Ignite Creation Date:
2025-12-25 @ 1:40 AM
Ignite Modification Date:
2026-02-25 @ 2:37 AM
Study NCT ID:
NCT02367794
Status:
COMPLETED
Last Update Posted:
2022-03-21
First Post:
2015-02-13
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
A Study of Atezolizumab in Combination With Carboplatin + Paclitaxel or Carboplatin + Nab-Paclitaxel Compared With Carboplatin + Nab-Paclitaxel in Participants With Stage IV Squamous Non-Small Cell Lung Cancer (NSCLC) [IMpower131]
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['Switzerland']}, 'interventionBrowseModule': {'meshes': [{'id': 'C000594389', 'term': 'atezolizumab'}, {'id': 'D000906', 'term': 'Antibodies'}, {'id': 'D016190', 'term': 'Carboplatin'}, {'id': 'C520255', 'term': '130-nm albumin-bound paclitaxel'}, {'id': 'D017239', 'term': 'Paclitaxel'}], 'ancestors': [{'id': 'D007136', 'term': 'Immunoglobulins'}, {'id': 'D007162', 'term': 'Immunoproteins'}, {'id': 'D001798', 'term': 'Blood Proteins'}, {'id': 'D011506', 'term': 'Proteins'}, {'id': 'D000602', 'term': 'Amino Acids, Peptides, and Proteins'}, {'id': 'D012712', 'term': 'Serum Globulins'}, {'id': 'D005916', 'term': 'Globulins'}, {'id': 'D056831', 'term': 'Coordination Complexes'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D043823', 'term': 'Taxoids'}, {'id': 'D043822', 'term': 'Cyclodecanes'}, {'id': 'D003516', 'term': 'Cycloparaffins'}, {'id': 'D006840', 'term': 'Hydrocarbons, Alicyclic'}, {'id': 'D006844', 'term': 'Hydrocarbons, Cyclic'}, {'id': 'D006838', 'term': 'Hydrocarbons'}, {'id': 'D004224', 'term': 'Diterpenes'}, {'id': 'D013729', 'term': 'Terpenes'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'genentech@druginfo.com', 'phone': '800-821-8590', 'title': 'Medical Communications', 'organization': 'Hoffmann-La Roche'}, 'certainAgreement': {'otherDetails': "The Study being conducted under this Agreement is part of the Overall Study. Investigator is free to publish in reputable journals or to present at professional conferences the results of the Study, but only after the first publication or presentation that involves the Overall Study. The Sponsor may request that Confidential Information be deleted and/or the publication be postponed in order to protect the Sponsor's intellectual property rights.", 'restrictionType': 'OTHER', 'piSponsorEmployee': False, 'restrictiveAgreement': True}}, 'adverseEventsModule': {'timeFrame': 'From the first study drug administration to the data cutoff date: 17 February 2021 (up to approximately 68 months).', 'description': 'All-cause mortality is reported for deaths that occurred during the study based on the ITT population, which included all randomized participants. Serious and other adverse events were reported based on the safety population, which included all randomized participants who received at least one dose of any study medication.', 'eventGroups': [{'id': 'EG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.', 'otherNumAtRisk': 334, 'deathsNumAtRisk': 340, 'otherNumAffected': 315, 'seriousNumAtRisk': 334, 'deathsNumAffected': 252, 'seriousNumAffected': 96}, {'id': 'EG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.', 'otherNumAtRisk': 334, 'deathsNumAtRisk': 343, 'otherNumAffected': 325, 'seriousNumAtRisk': 334, 'deathsNumAffected': 245, 'seriousNumAffected': 168}, {'id': 'EG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.', 'otherNumAtRisk': 332, 'deathsNumAtRisk': 338, 'otherNumAffected': 315, 'seriousNumAtRisk': 332, 'deathsNumAffected': 243, 'seriousNumAffected': 151}], 'otherEvents': [{'term': 'ANAEMIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 244, 'numAffected': 193}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 257, 'numAffected': 188}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 153, 'numAffected': 131}], 'organSystem': 'Blood and lymphatic system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'LEUKOPENIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 54, 'numAffected': 34}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 86, 'numAffected': 42}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 8, 'numAffected': 8}], 'organSystem': 'Blood and lymphatic system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'NEUTROPENIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 214, 'numAffected': 124}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 261, 'numAffected': 121}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 61, 'numAffected': 43}], 'organSystem': 'Blood and lymphatic system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'THROMBOCYTOPENIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 171, 'numAffected': 92}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 163, 'numAffected': 91}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 66, 'numAffected': 46}], 'organSystem': 'Blood and lymphatic system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'HYPOTHYROIDISM', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 2, 'numAffected': 2}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 40, 'numAffected': 34}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 30, 'numAffected': 27}], 'organSystem': 'Endocrine disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'ABDOMINAL PAIN', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 8, 'numAffected': 8}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 13, 'numAffected': 9}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 20, 'numAffected': 18}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'ABDOMINAL PAIN UPPER', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 17, 'numAffected': 17}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 17, 'numAffected': 13}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 15, 'numAffected': 12}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'CONSTIPATION', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 85, 'numAffected': 73}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 126, 'numAffected': 101}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 94, 'numAffected': 75}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'DIARRHOEA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 107, 'numAffected': 77}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 135, 'numAffected': 92}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 116, 'numAffected': 94}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'NAUSEA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 137, 'numAffected': 97}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 206, 'numAffected': 131}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 139, 'numAffected': 94}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'STOMATITIS', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 17, 'numAffected': 15}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 27, 'numAffected': 22}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 24, 'numAffected': 20}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'VOMITING', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 59, 'numAffected': 48}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 88, 'numAffected': 67}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 64, 'numAffected': 50}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'ASTHENIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 85, 'numAffected': 66}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 81, 'numAffected': 58}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 101, 'numAffected': 77}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'CHEST PAIN', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 19, 'numAffected': 18}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 31, 'numAffected': 25}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 35, 'numAffected': 28}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'FATIGUE', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 101, 'numAffected': 88}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 137, 'numAffected': 107}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 112, 'numAffected': 97}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'MALAISE', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 24, 'numAffected': 16}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 26, 'numAffected': 18}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 14, 'numAffected': 10}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'MUCOSAL INFLAMMATION', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 11, 'numAffected': 9}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 23, 'numAffected': 16}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 17, 'numAffected': 17}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'OEDEMA PERIPHERAL', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 25, 'numAffected': 22}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 32, 'numAffected': 25}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 28, 'numAffected': 23}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'PYREXIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 42, 'numAffected': 34}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 66, 'numAffected': 45}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 68, 'numAffected': 46}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'NASOPHARYNGITIS', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 11, 'numAffected': 9}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 28, 'numAffected': 21}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 35, 'numAffected': 23}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'PNEUMONIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 19, 'numAffected': 16}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 30, 'numAffected': 29}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 28, 'numAffected': 23}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'RESPIRATORY TRACT INFECTION', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 6, 'numAffected': 6}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 17, 'numAffected': 10}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 38, 'numAffected': 25}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'UPPER RESPIRATORY TRACT INFECTION', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 6, 'numAffected': 6}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 24, 'numAffected': 18}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 30, 'numAffected': 18}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'URINARY TRACT INFECTION', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 20, 'numAffected': 16}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 45, 'numAffected': 26}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 27, 'numAffected': 18}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'ALANINE AMINOTRANSFERASE INCREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 23, 'numAffected': 18}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 64, 'numAffected': 40}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 56, 'numAffected': 34}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'ASPARTATE AMINOTRANSFERASE INCREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 27, 'numAffected': 17}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 64, 'numAffected': 34}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 56, 'numAffected': 31}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'BLOOD ALKALINE PHOSPHATASE INCREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 8, 'numAffected': 8}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 18, 'numAffected': 17}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 33, 'numAffected': 25}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'BLOOD CREATININE INCREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 4, 'numAffected': 3}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 28, 'numAffected': 25}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 16, 'numAffected': 16}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'NEUTROPHIL COUNT DECREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 144, 'numAffected': 65}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 132, 'numAffected': 60}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 25, 'numAffected': 18}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'PLATELET COUNT DECREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 110, 'numAffected': 59}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 128, 'numAffected': 59}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 64, 'numAffected': 40}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'WEIGHT DECREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 14, 'numAffected': 14}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 38, 'numAffected': 32}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 22, 'numAffected': 21}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'WHITE BLOOD CELL COUNT DECREASED', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 68, 'numAffected': 36}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 64, 'numAffected': 32}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 19, 'numAffected': 12}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 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'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'HYPONATRAEMIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 5, 'numAffected': 5}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 17, 'numAffected': 11}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 22, 'numAffected': 17}], 'organSystem': 'Metabolism and nutrition disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'ARTHRALGIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 37, 'numAffected': 33}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 78, 'numAffected': 53}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 107, 'numAffected': 78}], 'organSystem': 'Musculoskeletal and connective tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'BACK PAIN', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 17, 'numAffected': 16}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 40, 'numAffected': 35}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 38, 'numAffected': 33}], 'organSystem': 'Musculoskeletal and connective tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'BONE PAIN', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 3, 'numAffected': 3}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 14, 'numAffected': 11}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 36, 'numAffected': 23}], 'organSystem': 'Musculoskeletal and connective tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MeDRA Version 23.1'}, {'term': 'MYALGIA', 'stats': [{'groupId': 'EG000', 'numAtRisk': 334, 'numEvents': 24, 'numAffected': 19}, {'groupId': 'EG001', 'numAtRisk': 334, 'numEvents': 23, 'numAffected': 22}, {'groupId': 'EG002', 'numAtRisk': 332, 'numEvents': 63, 'numAffected': 44}], 'organSystem': 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The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '5.6', 'groupId': 'OG000', 'lowerLimit': '5.5', 'upperLimit': '5.7'}, {'value': '6.5', 'groupId': 'OG001', 'lowerLimit': '5.7', 'upperLimit': '7.1'}, {'value': '5.6', 'groupId': 'OG002', 'lowerLimit': '5.5', 'upperLimit': '6.9'}]}]}], 'analyses': [{'pValue': '0.0006', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.75', 'ciLowerLimit': '0.64', 'ciUpperLimit': '0.88', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the ITT population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'PRIMARY', 'title': 'Overall Survival (OS) in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '340', 'groupId': 'OG000'}, {'value': '343', 'groupId': 'OG001'}, {'value': '338', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '13.5', 'groupId': 'OG000', 'lowerLimit': '12.2', 'upperLimit': '15.1'}, {'value': '14.2', 'groupId': 'OG001', 'lowerLimit': '12.3', 'upperLimit': '16.8'}, {'value': '12.6', 'groupId': 'OG002', 'lowerLimit': '11.6', 'upperLimit': '14.7'}]}]}], 'analyses': [{'pValue': '0.1581', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.88', 'ciLowerLimit': '0.73', 'ciUpperLimit': '1.05', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the ITT population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'OS in the in the Teff Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '322', 'groupId': 'OG000'}, {'value': '313', 'groupId': 'OG001'}, {'value': '308', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Teff >=-1.91', 'denoms': [{'units': 'Participants', 'counts': [{'value': '147', 'groupId': 'OG000'}, {'value': '124', 'groupId': 'OG001'}, {'value': '123', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '16.4', 'groupId': 'OG000', 'lowerLimit': '12.2', 'upperLimit': '19.7'}, {'value': '17.4', 'groupId': 'OG001', 'lowerLimit': '12.3', 'upperLimit': '23.8'}, {'value': '15.2', 'groupId': 'OG002', 'lowerLimit': '13.4', 'upperLimit': '22.8'}]}]}, {'title': 'Teff<-1.91', 'denoms': [{'units': 'Participants', 'counts': [{'value': '175', 'groupId': 'OG000'}, {'value': '189', 'groupId': 'OG001'}, {'value': '185', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '12.4', 'groupId': 'OG000', 'lowerLimit': '11.2', 'upperLimit': '14.3'}, {'value': '13.0', 'groupId': 'OG001', 'lowerLimit': '11.4', 'upperLimit': '14.8'}, {'value': '10.5', 'groupId': 'OG002', 'lowerLimit': '9.1', 'upperLimit': '12.6'}]}]}], 'analyses': [{'pValue': '0.4451', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.876', 'ciLowerLimit': '0.623', 'ciUpperLimit': '1.231', 'groupDescription': 'Teff \\>=-1.91 in ITT', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.7343', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.941', 'ciLowerLimit': '0.664', 'ciUpperLimit': '1.335', 'groupDescription': 'Teff \\>=-1.91 in ITT', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.6610', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.942', 'ciLowerLimit': '0.720', 'ciUpperLimit': '1.232', 'groupDescription': 'Teff \\<-1.91 Negative in ITT', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.0893', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.253', 'ciLowerLimit': '0.965', 'ciUpperLimit': '1.627', 'groupDescription': 'Teff \\<-1.91 Negative in ITT', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the in the Teff Population.', 'unitOfMeasure': 'Month', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'The Teff (\\>=-1.91) population and the Teff (\\<-1.91) population, defined as patients in the ITT population with Teff signature expression \\>=-1.91 and \\<-1.91, respectively.'}, {'type': 'SECONDARY', 'title': 'PFS as Determined by the Investigator Using RECIST v1.1 in the Teff Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '322', 'groupId': 'OG000'}, {'value': '313', 'groupId': 'OG001'}, {'value': '308', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Teff >=-1.91', 'denoms': [{'units': 'Participants', 'counts': [{'value': '147', 'groupId': 'OG000'}, {'value': '124', 'groupId': 'OG001'}, {'value': '123', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '5.6', 'groupId': 'OG000', 'lowerLimit': '5.1', 'upperLimit': '5.7'}, {'value': '7.0', 'groupId': 'OG001', 'lowerLimit': '5.5', 'upperLimit': '8.5'}, {'value': '7.0', 'groupId': 'OG002', 'lowerLimit': '5.6', 'upperLimit': '9.7'}]}]}, {'title': 'Teff<-1.91', 'denoms': [{'units': 'Participants', 'counts': [{'value': '175', 'groupId': 'OG000'}, {'value': '189', 'groupId': 'OG001'}, {'value': '185', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '5.7', 'groupId': 'OG000', 'lowerLimit': '5.5', 'upperLimit': '6.6'}, {'value': '6.2', 'groupId': 'OG001', 'lowerLimit': '5.6', 'upperLimit': '7.0'}, {'value': '5.5', 'groupId': 'OG002', 'lowerLimit': '4.5', 'upperLimit': '5.6'}]}]}], 'analyses': [{'pValue': '0.0006', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.61', 'ciLowerLimit': '0.46', 'ciUpperLimit': '0.81', 'groupDescription': 'Teff\\>=-1.91', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.630', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.06', 'ciLowerLimit': '0.84', 'ciUpperLimit': '1.33', 'groupDescription': 'Teff\\>=-1.91', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.258', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.88', 'ciLowerLimit': '0.70', 'ciUpperLimit': '1.10', 'groupDescription': 'Teff\\<-1.91', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.630', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.06', 'ciLowerLimit': '0.84', 'ciUpperLimit': '1.33', 'groupDescription': 'Teff\\<-1.91', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the Teff Population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'The Teff (\\>=-1.91) population and the Teff (\\<-1.91) population, defined as patients in the ITT population with Teff signature expression \\>=-1.91 and \\<-1.91, respectively.'}, {'type': 'SECONDARY', 'title': 'PFS as Determined by the Investigator Using RECIST v1.1 in the Tumor Cell (TC) 2/3 or Tumor-Infiltrating Immune Cell (IC) 2/3 Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '108', 'groupId': 'OG000'}, {'value': '115', 'groupId': 'OG001'}, {'value': '100', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '5.6', 'groupId': 'OG000', 'lowerLimit': '5.1', 'upperLimit': '5.7'}, {'value': '8.4', 'groupId': 'OG001', 'lowerLimit': '6.8', 'upperLimit': '10.4'}, {'value': '7.0', 'groupId': 'OG002', 'lowerLimit': '5.6', 'upperLimit': '8.3'}]}]}], 'analyses': [{'pValue': '<.0001', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.53', 'ciLowerLimit': '0.40', 'ciUpperLimit': '0.72', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}, {'pValue': '0.0018', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.61', 'ciLowerLimit': '0.45', 'ciUpperLimit': '0.84', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the Tumor Cell (TC) 2/3 or Tumor-Infiltrating Immune Cell (IC) 2/3 Population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'The PD-L1 TC2/3 or IC2/3 population is defined as particpants in the ITT population with PD-L1 TC2/3 or IC2/3 expression in baseline tumor tissue.'}, {'type': 'SECONDARY', 'title': 'PFS as Determined by the Investigator Using RECIST v1.1 in the TC1/2/3 or IC1/2/3 Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '169', 'groupId': 'OG000'}, {'value': '182', 'groupId': 'OG001'}, {'value': '167', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '5.6', 'groupId': 'OG000', 'lowerLimit': '5.3', 'upperLimit': '5.7'}, {'value': '7.1', 'groupId': 'OG001', 'lowerLimit': '5.8', 'upperLimit': '8.3'}, {'value': '7.0', 'groupId': 'OG002', 'lowerLimit': '5.6', 'upperLimit': '8.3'}]}]}], 'analyses': [{'pValue': '<.0001', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.61', 'ciLowerLimit': '0.48', 'ciUpperLimit': '0.77', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}, {'pValue': '<.0001', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.61', 'ciLowerLimit': '0.48', 'ciUpperLimit': '0.77', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the TC1/2/3 or IC1/2/3 Population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'The PD-L1 TC1/2/3 or IC1/2/3 population is defined as participants in the ITT population with PD-L1 TC1/2/3 or IC1/2/3 expression in baseline tumor tissue.'}, {'type': 'SECONDARY', 'title': 'OS in the TC2/3 or IC2/3 Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '108', 'groupId': 'OG000'}, {'value': '115', 'groupId': 'OG001'}, {'value': '100', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '14.5', 'groupId': 'OG000', 'lowerLimit': '12.1', 'upperLimit': '17.2'}, {'value': '20.4', 'groupId': 'OG001', 'lowerLimit': '13.8', 'upperLimit': '24.1'}, {'value': '14.8', 'groupId': 'OG002', 'lowerLimit': '11.1', 'upperLimit': '23.7'}]}]}], 'analyses': [{'pValue': '0.0518', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.725', 'ciLowerLimit': '0.524', 'ciUpperLimit': '1.004', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}, {'pValue': '0.2841', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.832', 'ciLowerLimit': '0.594', 'ciUpperLimit': '1.165', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause, in the TC2/3 or IC2/3 Population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'The PD-L1 TC2/3 or IC2/3 population is defined as particpants in the ITT population with PD-L1 TC2/3 or IC2/3 expression in baseline tumor tissue.'}, {'type': 'SECONDARY', 'title': 'OS in the TC1/2/3 or IC1/2/3 Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '169', 'groupId': 'OG000'}, {'value': '182', 'groupId': 'OG001'}, {'value': '167', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '15.0', 'groupId': 'OG000', 'lowerLimit': '12.4', 'upperLimit': '17.2'}, {'value': '14.8', 'groupId': 'OG001', 'lowerLimit': '12.1', 'upperLimit': '19.6'}, {'value': '14.9', 'groupId': 'OG002', 'lowerLimit': '12.5', 'upperLimit': '18.2'}]}]}], 'analyses': [{'pValue': '0.2956', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.871', 'ciLowerLimit': '0.671', 'ciUpperLimit': '1.129', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}, {'pValue': '0.2473', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.861', 'ciLowerLimit': '0.668', 'ciUpperLimit': '1.109', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the TC1/2/3 or IC1/2/3 Population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'The PD-L1 TC1/2/3 or IC1/2/3 population is defined as participants in the ITT population with PD-L1 TC1/2/3 or IC1/2/3 expression in baseline tumor tissue.'}, {'type': 'SECONDARY', 'title': 'Percentage of Participants With Objective Response as Determined by the Investigator Using RECIST v1.1 in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '339', 'groupId': 'OG000'}, {'value': '342', 'groupId': 'OG001'}, {'value': '337', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '41.0', 'groupId': 'OG000'}, {'value': '49.7', 'groupId': 'OG001'}, {'value': '49.3', 'groupId': 'OG002'}]}]}], 'analyses': [{'pValue': '0.0248', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Odds Ratio (OR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.41', 'ciLowerLimit': '1.04', 'ciUpperLimit': '1.91', 'statisticalMethod': 'Cochran-Mantel-Haenszel', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.0308', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Odds Ratio (OR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.40', 'ciLowerLimit': '1.03', 'ciUpperLimit': '1.90', 'statisticalMethod': 'Cochran-Mantel-Haenszel', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}], 'paramType': 'NUMBER', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'Proportion of participants with an objective response (CR or PR) in the ITT population.', 'unitOfMeasure': 'Percentage of participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'Duration of Response as Determined by the Investigator Using RECIST v1.1 in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '139', 'groupId': 'OG000'}, {'value': '170', 'groupId': 'OG001'}, {'value': '166', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '5.2', 'groupId': 'OG000', 'lowerLimit': '4.4', 'upperLimit': '5.6'}, {'value': '7.2', 'groupId': 'OG001', 'lowerLimit': '6.8', 'upperLimit': '9.5'}, {'value': '7.0', 'groupId': 'OG002', 'lowerLimit': '5.7', 'upperLimit': '8.3'}]}]}], 'analyses': [{'pValue': '<.0001', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.530', 'ciLowerLimit': '0.408', 'ciUpperLimit': '0.689', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}, {'pValue': '0.0007', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.640', 'ciLowerLimit': '0.493', 'ciUpperLimit': '0.831', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Unstratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'Duration of response is defined as the time from the first documented objective response to documented PD or death from any cause, whichever occurred first, in the ITT Population.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'Event Free Rate at 1 and 2 Years in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '184', 'groupId': 'OG000'}, {'value': '187', 'groupId': 'OG001'}, {'value': '170', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': '1 Year', 'denoms': [{'units': 'Participants', 'counts': [{'value': '184', 'groupId': 'OG000'}, {'value': '187', 'groupId': 'OG001'}, {'value': '170', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '56.28', 'groupId': 'OG000'}, {'value': '56.34', 'groupId': 'OG001'}, {'value': '52.30', 'groupId': 'OG002'}]}]}, {'title': '2 Year', 'denoms': [{'units': 'Participants', 'counts': [{'value': '49', 'groupId': 'OG000'}, {'value': '68', 'groupId': 'OG001'}, {'value': '50', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '26.58', 'groupId': 'OG000'}, {'value': '32.51', 'groupId': 'OG001'}, {'value': '27.79', 'groupId': 'OG002'}]}]}], 'analyses': [{'pValue': '0.9871', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Difference in Event Free Rate', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.06', 'ciLowerLimit': '-7.48', 'ciUpperLimit': '7.61', 'groupDescription': 'Event Free Rate (%) at Year 1', 'statisticalMethod': 'Z-test', 'nonInferiorityType': 'SUPERIORITY'}, {'pValue': '0.1133', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Difference in Event Free Rate', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '5.93', 'ciLowerLimit': '-1.41', 'ciUpperLimit': '13.26', 'groupDescription': 'Event Free Rate (%) at Year 2', 'statisticalMethod': 'Z-test', 'nonInferiorityType': 'SUPERIORITY'}, {'pValue': '0.3072', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Difference in Event Free Rate', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '-3.97', 'ciLowerLimit': '-11.60', 'ciUpperLimit': '3.65', 'groupDescription': 'Event Free Rate (%) at Year 1', 'statisticalMethod': 'Z-test', 'nonInferiorityType': 'SUPERIORITY'}, {'pValue': '0.7430', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Difference in Event Free Rate', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.21', 'ciLowerLimit': '-6.01', 'ciUpperLimit': '8.42', 'groupDescription': 'Event Free Rate (%) at Year 2', 'statisticalMethod': 'Z-test', 'nonInferiorityType': 'SUPERIORITY'}], 'paramType': 'NUMBER', 'timeFrame': '1 and 2 years', 'description': 'Event free rate at 1 and 2 years is defined as the proportion of participants alive at 1 and 2 years after randomization estimated using Kaplan-Meier (KM) methodology for the ITT population.', 'unitOfMeasure': 'Percentage of participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Participants still alive at 1 or 2 years after randomization from the ITT population.'}, {'type': 'SECONDARY', 'title': 'Time to Deterioration (TTD) in Patient-reported Lung Cancer Symptoms Using EORTC QLQ-C30 Symptom Subscales in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '340', 'groupId': 'OG000'}, {'value': '343', 'groupId': 'OG001'}, {'value': '338', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '3.2', 'groupId': 'OG000', 'lowerLimit': '2.6', 'upperLimit': '4.1'}, {'value': '4.2', 'groupId': 'OG001', 'lowerLimit': '3.2', 'upperLimit': '5.6'}, {'value': '3.0', 'groupId': 'OG002', 'lowerLimit': '2.6', 'upperLimit': '3.9'}]}]}], 'analyses': [{'pValue': '0.0461', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.797', 'ciLowerLimit': '0.638', 'ciUpperLimit': '0.996', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.7295', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '1.040', 'ciLowerLimit': '0.834', 'ciUpperLimit': '1.296', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'TTD in Patient-reported Lung Cancer Symptoms Using EORTC QLQ-C30 Symptom Subscales in the ITT Population. The EORTC QLQ-C30 is a validated and reliable self-report measure that consists of 30 questions that assess five aspects of patient functioning (physical, emotional, role, cognitive, and social), three symptom scales (fatigue, nausea and vomiting, pain), global health/quality of life, and six single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). EORTC scales and single-item measures will be linearly transformed so that each score has a range of 0-100. A high score for a functional scale represents a high or healthy level of functioning, and a high score for the global health status and HRQoL represents a high HRQoL; however, a high score for a symptom scale or item represents a high level of symptomatology or problems.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'TTD in Patient-reported Lung Cancer Symptoms Using EORTC QLQ-LC13 Symptom Subscales in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '340', 'groupId': 'OG000'}, {'value': '343', 'groupId': 'OG001'}, {'value': '338', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '2.6', 'groupId': 'OG000', 'lowerLimit': '2.2', 'upperLimit': '3.0'}, {'value': '3.4', 'groupId': 'OG001', 'lowerLimit': '2.7', 'upperLimit': '5.1'}, {'value': '2.8', 'groupId': 'OG002', 'lowerLimit': '2.1', 'upperLimit': '3.7'}]}]}], 'analyses': [{'pValue': '0.0942', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.828', 'ciLowerLimit': '0.663', 'ciUpperLimit': '1.033', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}, {'pValue': '0.7709', 'groupIds': ['OG000', 'OG002'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.968', 'ciLowerLimit': '0.776', 'ciUpperLimit': '1.207', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after the first participant enrolled', 'description': 'TTD was documented for a 3-symptom composite endpoint using the following EORTC QLQ-LC13 symptom scores: cough, chest pain, and dyspnea multi--item scale. In this instance, symptom deterioration will be determined as a \\>= 10-point increase above baseline in any of the listed symptom scores, whichever occurs first (cough, chest pain, and dyspnea multi-item scale). Confirmed clinically meaningful symptom deterioration will need to be held for the original symptom; a \\>= 10-point increase above baseline in a symptom score must be held for at least two consecutive assessments or an initial\\>=10-point increase above baseline followed by death within 3 weeks from the last assessment. A \\>= 10-point change in the EORTC scale score is perceived by patients as clinically significant.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'Change From Baseline in Patient-reported Lung Cancer Symptoms Score Using the SILC Scale Symptom Severity Score in the ITT Population', 'denoms': [{'units': 'Participants', 'counts': [{'value': '189', 'groupId': 'OG000'}, {'value': '215', 'groupId': 'OG001'}, {'value': '195', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Chest Pain, Week 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '171', 'groupId': 'OG000'}, {'value': '192', 'groupId': 'OG001'}, {'value': '166', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.04', 'spread': '0.93', 'groupId': 'OG000'}, {'value': '0.14', 'spread': '0.87', 'groupId': 'OG001'}, {'value': '0.44', 'spread': '1.03', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 2', 'denoms': [{'units': 'Participants', 'counts': [{'value': '160', 'groupId': 'OG000'}, {'value': '186', 'groupId': 'OG001'}, {'value': '165', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.08', 'spread': '0.89', 'groupId': 'OG000'}, {'value': '0.09', 'spread': '0.98', 'groupId': 'OG001'}, {'value': '0.28', 'spread': '1.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 3', 'denoms': [{'units': 'Participants', 'counts': [{'value': '165', 'groupId': 'OG000'}, {'value': '175', 'groupId': 'OG001'}, {'value': '165', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.14', 'spread': '0.95', 'groupId': 'OG000'}, {'value': '-0.03', 'spread': '0.78', 'groupId': 'OG001'}, {'value': '-0.05', 'spread': '1.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 4', 'denoms': [{'units': 'Participants', 'counts': [{'value': '157', 'groupId': 'OG000'}, {'value': '173', 'groupId': 'OG001'}, {'value': '169', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.19', 'spread': '0.98', 'groupId': 'OG000'}, {'value': '-0.05', 'spread': '0.98', 'groupId': 'OG001'}, {'value': '0.09', 'spread': '1.12', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 5', 'denoms': [{'units': 'Participants', 'counts': [{'value': '160', 'groupId': 'OG000'}, {'value': '172', 'groupId': 'OG001'}, {'value': '159', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.17', 'spread': '1.10', 'groupId': 'OG000'}, {'value': '-0.08', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.16', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 6', 'denoms': [{'units': 'Participants', 'counts': [{'value': '151', 'groupId': 'OG000'}, {'value': '170', 'groupId': 'OG001'}, {'value': '161', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.35', 'spread': '1.08', 'groupId': 'OG000'}, {'value': '-0.13', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.20', 'spread': '1.02', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 7', 'denoms': [{'units': 'Participants', 'counts': [{'value': '138', 'groupId': 'OG000'}, {'value': '166', 'groupId': 'OG001'}, {'value': '143', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.38', 'spread': '1.12', 'groupId': 'OG000'}, {'value': '-0.18', 'spread': '0.92', 'groupId': 'OG001'}, {'value': '-0.14', 'spread': '1.16', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 8', 'denoms': [{'units': 'Participants', 'counts': [{'value': '140', 'groupId': 'OG000'}, {'value': '162', 'groupId': 'OG001'}, {'value': '152', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.35', 'spread': '1.12', 'groupId': 'OG000'}, {'value': '-0.17', 'spread': '1.02', 'groupId': 'OG001'}, {'value': '-0.17', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 9', 'denoms': [{'units': 'Participants', 'counts': [{'value': '135', 'groupId': 'OG000'}, {'value': '162', 'groupId': 'OG001'}, {'value': '143', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.36', 'spread': '1.00', 'groupId': 'OG000'}, {'value': '-0.19', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '-0.21', 'spread': '1.10', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 10', 'denoms': [{'units': 'Participants', 'counts': [{'value': '133', 'groupId': 'OG000'}, {'value': '158', 'groupId': 'OG001'}, {'value': '146', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.20', 'spread': '1.09', 'groupId': 'OG000'}, {'value': '-0.16', 'spread': '1.00', 'groupId': 'OG001'}, {'value': '-0.08', 'spread': '1.19', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 11', 'denoms': [{'units': 'Participants', 'counts': [{'value': '132', 'groupId': 'OG000'}, {'value': '157', 'groupId': 'OG001'}, {'value': '137', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.27', 'spread': '1.08', 'groupId': 'OG000'}, {'value': '-0.24', 'spread': '0.91', 'groupId': 'OG001'}, {'value': '-0.09', 'spread': '1.16', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 12', 'denoms': [{'units': 'Participants', 'counts': [{'value': '128', 'groupId': 'OG000'}, {'value': '151', 'groupId': 'OG001'}, {'value': '136', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.34', 'spread': '1.05', 'groupId': 'OG000'}, {'value': '-0.21', 'spread': '1.01', 'groupId': 'OG001'}, {'value': '-0.30', 'spread': '1.05', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 13', 'denoms': [{'units': 'Participants', 'counts': [{'value': '117', 'groupId': 'OG000'}, {'value': '144', 'groupId': 'OG001'}, {'value': '130', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.31', 'spread': '1.24', 'groupId': 'OG000'}, {'value': '-0.22', 'spread': '1.02', 'groupId': 'OG001'}, {'value': '-0.17', 'spread': '1.10', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 14', 'denoms': [{'units': 'Participants', 'counts': [{'value': '105', 'groupId': 'OG000'}, {'value': '139', 'groupId': 'OG001'}, {'value': '138', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.32', 'spread': '1.18', 'groupId': 'OG000'}, {'value': '-0.24', 'spread': '0.88', 'groupId': 'OG001'}, {'value': '-0.15', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 15', 'denoms': [{'units': 'Participants', 'counts': [{'value': '97', 'groupId': 'OG000'}, {'value': '143', 'groupId': 'OG001'}, {'value': '132', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.45', 'spread': '1.19', 'groupId': 'OG000'}, {'value': '-0.28', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.17', 'spread': '1.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 16', 'denoms': [{'units': 'Participants', 'counts': [{'value': '102', 'groupId': 'OG000'}, {'value': '138', 'groupId': 'OG001'}, {'value': '121', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.28', 'spread': '1.10', 'groupId': 'OG000'}, {'value': '-0.14', 'spread': '1.00', 'groupId': 'OG001'}, {'value': '-0.23', 'spread': '1.10', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 17', 'denoms': [{'units': 'Participants', 'counts': [{'value': '101', 'groupId': 'OG000'}, {'value': '135', 'groupId': 'OG001'}, {'value': '129', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.32', 'spread': '1.11', 'groupId': 'OG000'}, {'value': '-0.17', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.24', 'spread': '1.10', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 18', 'denoms': [{'units': 'Participants', 'counts': [{'value': '93', 'groupId': 'OG000'}, {'value': '141', 'groupId': 'OG001'}, {'value': '129', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.28', 'spread': '1.08', 'groupId': 'OG000'}, {'value': '-0.13', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.17', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 19', 'denoms': [{'units': 'Participants', 'counts': [{'value': '85', 'groupId': 'OG000'}, {'value': '129', 'groupId': 'OG001'}, {'value': '118', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.18', 'spread': '1.09', 'groupId': 'OG000'}, {'value': '-0.10', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.16', 'spread': '1.07', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 20', 'denoms': [{'units': 'Participants', 'counts': [{'value': '75', 'groupId': 'OG000'}, {'value': '130', 'groupId': 'OG001'}, {'value': '114', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.23', 'spread': '1.07', 'groupId': 'OG000'}, {'value': '-0.15', 'spread': '0.94', 'groupId': 'OG001'}, {'value': '-0.17', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 21', 'denoms': [{'units': 'Participants', 'counts': [{'value': '69', 'groupId': 'OG000'}, {'value': '129', 'groupId': 'OG001'}, {'value': '113', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.37', 'spread': '1.02', 'groupId': 'OG000'}, {'value': '-0.07', 'spread': '1.02', 'groupId': 'OG001'}, {'value': '-0.18', 'spread': '1.14', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 22', 'denoms': [{'units': 'Participants', 'counts': [{'value': '79', 'groupId': 'OG000'}, {'value': '125', 'groupId': 'OG001'}, {'value': '109', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.27', 'spread': '1.18', 'groupId': 'OG000'}, {'value': '-0.08', 'spread': '1.01', 'groupId': 'OG001'}, {'value': '-0.14', 'spread': '1.16', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 23', 'denoms': [{'units': 'Participants', 'counts': [{'value': '70', 'groupId': 'OG000'}, {'value': '128', 'groupId': 'OG001'}, {'value': '106', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.29', 'spread': '1.16', 'groupId': 'OG000'}, {'value': '0.04', 'spread': '0.96', 'groupId': 'OG001'}, {'value': '-0.10', 'spread': '1.07', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 24', 'denoms': [{'units': 'Participants', 'counts': [{'value': '67', 'groupId': 'OG000'}, {'value': '121', 'groupId': 'OG001'}, {'value': '105', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.43', 'spread': '1.15', 'groupId': 'OG000'}, {'value': '-0.15', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '-0.17', 'spread': '1.14', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 25', 'denoms': [{'units': 'Participants', 'counts': [{'value': '48', 'groupId': 'OG000'}, {'value': '118', 'groupId': 'OG001'}, {'value': '104', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.25', 'spread': '1.24', 'groupId': 'OG000'}, {'value': '-0.17', 'spread': '1.06', 'groupId': 'OG001'}, {'value': '-0.20', 'spread': '1.10', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 26', 'denoms': [{'units': 'Participants', 'counts': [{'value': '48', 'groupId': 'OG000'}, {'value': '111', 'groupId': 'OG001'}, {'value': '99', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.50', 'spread': '1.20', 'groupId': 'OG000'}, {'value': '-0.06', 'spread': '1.08', 'groupId': 'OG001'}, {'value': '-0.11', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 27', 'denoms': [{'units': 'Participants', 'counts': [{'value': '42', 'groupId': 'OG000'}, {'value': '110', 'groupId': 'OG001'}, {'value': '95', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.35', 'spread': '1.29', 'groupId': 'OG000'}, {'value': '-0.17', 'spread': '1.03', 'groupId': 'OG001'}, {'value': '0.04', 'spread': '1.14', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 28', 'denoms': [{'units': 'Participants', 'counts': [{'value': '41', 'groupId': 'OG000'}, {'value': '103', 'groupId': 'OG001'}, {'value': '88', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.22', 'spread': '1.27', 'groupId': 'OG000'}, {'value': '-0.12', 'spread': '1.09', 'groupId': 'OG001'}, {'value': '-0.19', 'spread': '1.24', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 29', 'denoms': [{'units': 'Participants', 'counts': [{'value': '38', 'groupId': 'OG000'}, {'value': '100', 'groupId': 'OG001'}, {'value': '89', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.30', 'spread': '1.23', 'groupId': 'OG000'}, {'value': '-0.11', 'spread': '0.96', 'groupId': 'OG001'}, {'value': '-0.18', 'spread': '1.11', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 30', 'denoms': [{'units': 'Participants', 'counts': [{'value': '46', 'groupId': 'OG000'}, {'value': '104', 'groupId': 'OG001'}, {'value': '86', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.15', 'spread': '1.36', 'groupId': 'OG000'}, {'value': '-0.21', 'spread': '1.02', 'groupId': 'OG001'}, {'value': '-0.08', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 31', 'denoms': [{'units': 'Participants', 'counts': [{'value': '35', 'groupId': 'OG000'}, {'value': '97', 'groupId': 'OG001'}, {'value': '77', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.49', 'spread': '1.25', 'groupId': 'OG000'}, {'value': '-0.16', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.15', 'spread': '1.08', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 32', 'denoms': [{'units': 'Participants', 'counts': [{'value': '29', 'groupId': 'OG000'}, {'value': '91', 'groupId': 'OG001'}, {'value': '70', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.29', 'spread': '1.16', 'groupId': 'OG000'}, {'value': '-0.15', 'spread': '0.88', 'groupId': 'OG001'}, {'value': '-0.16', 'spread': '1.01', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 33', 'denoms': [{'units': 'Participants', 'counts': [{'value': '29', 'groupId': 'OG000'}, {'value': '93', 'groupId': 'OG001'}, {'value': '68', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.29', 'spread': '1.35', 'groupId': 'OG000'}, {'value': '-0.20', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '-0.10', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 34', 'denoms': [{'units': 'Participants', 'counts': [{'value': '33', 'groupId': 'OG000'}, {'value': '92', 'groupId': 'OG001'}, {'value': '73', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.15', 'spread': '1.42', 'groupId': 'OG000'}, {'value': '-0.04', 'spread': '0.89', 'groupId': 'OG001'}, {'value': '0.02', 'spread': '1.16', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 35', 'denoms': [{'units': 'Participants', 'counts': [{'value': '33', 'groupId': 'OG000'}, {'value': '90', 'groupId': 'OG001'}, {'value': '72', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.26', 'spread': '1.31', 'groupId': 'OG000'}, {'value': '-0.14', 'spread': '0.88', 'groupId': 'OG001'}, {'value': '-0.19', 'spread': '1.09', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 36', 'denoms': [{'units': 'Participants', 'counts': [{'value': '31', 'groupId': 'OG000'}, {'value': '83', 'groupId': 'OG001'}, {'value': '64', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.24', 'spread': '1.34', 'groupId': 'OG000'}, {'value': '-0.06', 'spread': '0.88', 'groupId': 'OG001'}, {'value': '-0.06', 'spread': '1.12', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 37', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}, {'value': '84', 'groupId': 'OG001'}, {'value': '65', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.27', 'spread': '1.37', 'groupId': 'OG000'}, {'value': '0.05', 'spread': '1.06', 'groupId': 'OG001'}, {'value': '-0.08', 'spread': '1.08', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 38', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}, {'value': '86', 'groupId': 'OG001'}, {'value': '65', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.19', 'spread': '1.30', 'groupId': 'OG000'}, {'value': '-0.09', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '-0.14', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 39', 'denoms': [{'units': 'Participants', 'counts': [{'value': '25', 'groupId': 'OG000'}, {'value': '75', 'groupId': 'OG001'}, {'value': '68', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.06', 'spread': '1.53', 'groupId': 'OG000'}, {'value': '-0.18', 'spread': '0.96', 'groupId': 'OG001'}, {'value': '-0.13', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 40', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}, {'value': '74', 'groupId': 'OG001'}, {'value': '62', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.06', 'spread': '1.31', 'groupId': 'OG000'}, {'value': '-0.11', 'spread': '0.85', 'groupId': 'OG001'}, {'value': '-0.06', 'spread': '1.01', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 41', 'denoms': [{'units': 'Participants', 'counts': [{'value': '22', 'groupId': 'OG000'}, {'value': '69', 'groupId': 'OG001'}, {'value': '60', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.14', 'spread': '1.21', 'groupId': 'OG000'}, {'value': '-0.14', 'spread': '0.92', 'groupId': 'OG001'}, {'value': '-0.13', 'spread': '1.05', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 42', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}, {'value': '77', 'groupId': 'OG001'}, {'value': '60', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.10', 'spread': '1.50', 'groupId': 'OG000'}, {'value': '-0.05', 'spread': '0.94', 'groupId': 'OG001'}, {'value': '-0.11', 'spread': '1.02', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 43', 'denoms': [{'units': 'Participants', 'counts': [{'value': '23', 'groupId': 'OG000'}, {'value': '72', 'groupId': 'OG001'}, {'value': '58', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.13', 'spread': '1.59', 'groupId': 'OG000'}, {'value': '-0.08', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '0.05', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 44', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '93', 'groupId': 'OG001'}, {'value': '60', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.08', 'spread': '1.52', 'groupId': 'OG000'}, {'value': '-0.25', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '-0.10', 'spread': '1.07', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 45', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '64', 'groupId': 'OG001'}, {'value': '51', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.15', 'spread': '1.70', 'groupId': 'OG000'}, {'value': '-0.21', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '-0.05', 'spread': '1.20', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 46', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '61', 'groupId': 'OG001'}, {'value': '53', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'spread': '1.39', 'groupId': 'OG000'}, {'value': '-0.16', 'spread': '1.04', 'groupId': 'OG001'}, {'value': '-0.07', 'spread': '1.33', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 47', 'denoms': [{'units': 'Participants', 'counts': [{'value': '20', 'groupId': 'OG000'}, {'value': '64', 'groupId': 'OG001'}, {'value': '48', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.18', 'spread': '1.29', 'groupId': 'OG000'}, {'value': '-0.16', 'spread': '0.99', 'groupId': 'OG001'}, {'value': '0.04', 'spread': '1.29', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 48', 'denoms': [{'units': 'Participants', 'counts': [{'value': '19', 'groupId': 'OG000'}, {'value': '62', 'groupId': 'OG001'}, {'value': '52', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.08', 'spread': '1.53', 'groupId': 'OG000'}, {'value': '-0.17', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '0.00', 'spread': '1.32', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 49', 'denoms': [{'units': 'Participants', 'counts': [{'value': '13', 'groupId': 'OG000'}, {'value': '57', 'groupId': 'OG001'}, {'value': '45', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.23', 'spread': '1.59', 'groupId': 'OG000'}, {'value': 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'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 67', 'denoms': [{'units': 'Participants', 'counts': [{'value': '5', 'groupId': 'OG000'}, {'value': '33', 'groupId': 'OG001'}, {'value': '20', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.50', 'spread': '1.27', 'groupId': 'OG000'}, {'value': '-0.08', 'spread': '1.04', 'groupId': 'OG001'}, {'value': '-0.43', 'spread': '1.27', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 68', 'denoms': [{'units': 'Participants', 'counts': [{'value': '6', 'groupId': 'OG000'}, {'value': '33', 'groupId': 'OG001'}, {'value': '19', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.08', 'spread': '1.77', 'groupId': 'OG000'}, {'value': '-0.09', 'spread': '1.02', 'groupId': 'OG001'}, {'value': '-0.53', 'spread': '1.23', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 69', 'denoms': [{'units': 'Participants', 'counts': [{'value': '5', 'groupId': 'OG000'}, {'value': '31', 'groupId': 'OG001'}, {'value': '18', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.70', 'spread': '1.60', 'groupId': 'OG000'}, {'value': '-0.15', 'spread': '1.08', 'groupId': 'OG001'}, {'value': '-0.03', 'spread': '1.14', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 70', 'denoms': [{'units': 'Participants', 'counts': [{'value': '5', 'groupId': 'OG000'}, {'value': '32', 'groupId': 'OG001'}, {'value': '19', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.30', 'spread': '1.79', 'groupId': 'OG000'}, {'value': '-0.06', 'spread': '0.97', 'groupId': 'OG001'}, {'value': '-0.32', 'spread': '1.08', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 71', 'denoms': [{'units': 'Participants', 'counts': [{'value': '6', 'groupId': 'OG000'}, {'value': '27', 'groupId': 'OG001'}, {'value': '15', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.08', 'spread': '1.72', 'groupId': 'OG000'}, {'value': '-0.13', 'spread': '0.91', 'groupId': 'OG001'}, {'value': 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'groupId': 'OG001'}, {'value': '-0.21', 'spread': '1.25', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 77', 'denoms': [{'units': 'Participants', 'counts': [{'value': '6', 'groupId': 'OG000'}, {'value': '22', 'groupId': 'OG001'}, {'value': '10', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'spread': '1.76', 'groupId': 'OG000'}, {'value': '0.00', 'spread': '1.15', 'groupId': 'OG001'}, {'value': '-0.05', 'spread': '1.21', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 78', 'denoms': [{'units': 'Participants', 'counts': [{'value': '7', 'groupId': 'OG000'}, {'value': '22', 'groupId': 'OG001'}, {'value': '11', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.07', 'spread': '1.62', 'groupId': 'OG000'}, {'value': '-0.11', 'spread': '1.11', 'groupId': 'OG001'}, {'value': '0.00', 'spread': '1.02', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 79', 'denoms': [{'units': 'Participants', 'counts': [{'value': '6', 'groupId': 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{'value': '-0.37', 'spread': '0.95', 'groupId': 'OG001'}, {'value': '0.33', 'spread': '1.37', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 87', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '12', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '1.00', 'spread': '1.73', 'groupId': 'OG000'}, {'value': '-0.25', 'spread': '1.10', 'groupId': 'OG001'}, {'value': '0.13', 'spread': '0.99', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 88', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '15', 'groupId': 'OG001'}, {'value': '7', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.83', 'spread': '1.44', 'groupId': 'OG000'}, {'value': '-0.20', 'spread': '1.22', 'groupId': 'OG001'}, {'value': '0.00', 'spread': '1.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 89', 'denoms': [{'units': 'Participants', 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'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '7', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.67', 'spread': '2.08', 'groupId': 'OG000'}, {'value': '0.00', 'spread': '1.53', 'groupId': 'OG001'}, {'value': '0.07', 'spread': '1.02', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 100', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '1.25', 'spread': '1.77', 'groupId': 'OG000'}, {'value': '-0.15', 'spread': '1.43', 'groupId': 'OG001'}, {'value': '0.00', 'spread': '1.20', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 101', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '7', 'groupId': 'OG002'}]}], 'categories': [{'measurements': 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Pain, Week 104', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '8', 'groupId': 'OG001'}, {'value': '4', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.25', 'spread': '0.35', 'groupId': 'OG000'}, {'value': '-0.56', 'spread': '1.05', 'groupId': 'OG001'}, {'value': '0.00', 'spread': '1.41', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 105', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '6', 'groupId': 'OG001'}, {'value': '6', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.50', 'spread': '0.00', 'groupId': 'OG000'}, {'value': '-0.50', 'spread': '0.84', 'groupId': 'OG001'}, {'value': '0.00', 'spread': '1.10', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 106', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '9', 'groupId': 'OG001'}, {'value': '5', 'groupId': 'OG002'}]}], 'categories': 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'OG002'}]}]}, {'title': 'Chest Pain, Week 109', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '5', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.50', 'spread': '0.71', 'groupId': 'OG000'}, {'value': '-0.90', 'spread': '1.24', 'groupId': 'OG001'}, {'value': '0.25', 'spread': '1.77', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 110', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}, {'value': '4', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'spread': '0.71', 'groupId': 'OG000'}, {'value': '-0.50', 'spread': '1.32', 'groupId': 'OG001'}, {'value': '-0.38', 'spread': '1.11', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 111', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '4', 'groupId': 'OG001'}, {'value': '4', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.25', 'spread': '0.35', 'groupId': 'OG000'}, {'value': '-0.25', 'spread': '1.26', 'groupId': 'OG001'}, {'value': '-0.38', 'spread': '0.48', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 112', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.50', 'spread': '0.00', 'groupId': 'OG000'}, {'value': '-0.67', 'spread': '1.15', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 113', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '4', 'groupId': 'OG001'}, {'value': '3', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG000'}, {'value': '-0.50', 'spread': '1.00', 'groupId': 'OG001'}, {'value': '-0.67', 'spread': '0.58', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 114', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.25', 'spread': '1.06', 'groupId': 'OG000'}, {'value': '-0.50', 'spread': '1.32', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 115', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '4', 'groupId': 'OG001'}, {'value': '3', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.25', 'spread': '1.06', 'groupId': 'OG000'}, {'value': '-0.50', 'spread': '1.00', 'groupId': 'OG001'}, {'value': '-0.67', 'spread': '0.58', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 116', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}, {'value': '3', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.50', 'spread': '0.71', 'groupId': 'OG000'}, {'value': '-0.67', 'spread': '1.15', 'groupId': 'OG001'}, {'value': '-0.67', 'spread': '0.58', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 117', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '2', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.25', 'spread': '1.06', 'groupId': 'OG000'}, {'value': '-1.00', 'spread': '1.41', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 118', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG000'}, {'value': '0.00', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 119', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 120', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 121', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 122', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG001'}, {'value': '-1.00', 'spread': '0.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 123', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG001'}, {'value': '-1.00', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 124', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.00', 'groupId': 'OG001'}, {'value': '-0.50', 'groupId': 'OG002'}]}]}, {'title': 'Chest Pain, Week 125', 'denoms': [{'units': 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'counts': [{'value': '52', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.10', 'spread': '1.23', 'groupId': 'OG000'}]}]}, {'title': 'Chest Pain, Survival Follow-Up Month 3', 'denoms': [{'units': 'Participants', 'counts': [{'value': '40', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.09', 'spread': '1.13', 'groupId': 'OG000'}]}]}, {'title': 'Chest Pain, Survival Follow-Up Month 4', 'denoms': [{'units': 'Participants', 'counts': [{'value': '32', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.13', 'spread': '1.15', 'groupId': 'OG000'}]}]}, {'title': 'Chest Pain, Survival Follow-Up Month 5', 'denoms': [{'units': 'Participants', 'counts': [{'value': '26', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.02', 'spread': '1.34', 'groupId': 'OG000'}]}]}, {'title': 'Chest Pain, Survival Follow-Up Month 6', 'denoms': [{'units': 'Participants', 'counts': [{'value': '23', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.22', 'spread': '0.99', 'groupId': 'OG000'}]}]}, {'title': 'Chest Pain, Survival Follow-Up Month 7', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.33', 'spread': '0.58', 'groupId': 'OG000'}]}]}, {'title': 'Chest Pain, Survival Follow-Up Month 8', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': 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'groupId': 'OG001'}, {'value': '-0.19', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Cough, Week 6', 'denoms': [{'units': 'Participants', 'counts': [{'value': '151', 'groupId': 'OG000'}, {'value': '170', 'groupId': 'OG001'}, {'value': '161', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.27', 'spread': '1.05', 'groupId': 'OG000'}, {'value': '-0.22', 'spread': '1.01', 'groupId': 'OG001'}, {'value': '-0.35', 'spread': '1.11', 'groupId': 'OG002'}]}]}, {'title': 'Cough, Week 7', 'denoms': [{'units': 'Participants', 'counts': [{'value': '138', 'groupId': 'OG000'}, {'value': '166', 'groupId': 'OG001'}, {'value': '143', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.27', 'spread': '1.06', 'groupId': 'OG000'}, {'value': '-0.27', 'spread': '1.07', 'groupId': 'OG001'}, {'value': '-0.47', 'spread': '1.11', 'groupId': 'OG002'}]}]}, {'title': 'Cough, Week 8', 'denoms': [{'units': 'Participants', 'counts': [{'value': '140', 'groupId': 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'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.80', 'groupId': 'OG001'}, {'value': '-1.40', 'spread': '0.28', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 120', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.80', 'groupId': 'OG001'}, {'value': '-1.10', 'spread': '0.42', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 121', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.80', 'groupId': 'OG001'}, {'value': '-1.30', 'spread': '0.14', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 122', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '2', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.80', 'groupId': 'OG001'}, {'value': '-1.30', 'spread': '0.14', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 123', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.80', 'groupId': 'OG001'}, {'value': '-1.00', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 124', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-0.80', 'groupId': 'OG001'}, {'value': '-1.20', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 125', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-1.00', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 126', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-1.20', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Week 127', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '1', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '-1.20', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Time of First Pd', 'denoms': [{'units': 'Participants', 'counts': [{'value': '103', 'groupId': 'OG000'}, {'value': '107', 'groupId': 'OG001'}, {'value': '106', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.38', 'spread': '1.06', 'groupId': 'OG000'}, {'value': '0.42', 'spread': '0.95', 'groupId': 'OG001'}, {'value': '0.27', 'spread': '1.13', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Time of Last Tx Dose', 'denoms': [{'units': 'Participants', 'counts': [{'value': '161', 'groupId': 'OG000'}, {'value': '172', 'groupId': 'OG001'}, {'value': '151', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.43', 'spread': '0.91', 'groupId': 'OG000'}, {'value': '0.28', 'spread': '1.01', 'groupId': 'OG001'}, {'value': '0.28', 'spread': '1.00', 'groupId': 'OG002'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '86', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.56', 'spread': '1.09', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 2', 'denoms': [{'units': 'Participants', 'counts': [{'value': '52', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.71', 'spread': '0.89', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 3', 'denoms': [{'units': 'Participants', 'counts': [{'value': '40', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.67', 'spread': '1.06', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 4', 'denoms': [{'units': 'Participants', 'counts': [{'value': '32', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.57', 'spread': '0.91', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 5', 'denoms': [{'units': 'Participants', 'counts': [{'value': '26', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.66', 'spread': '1.02', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 6', 'denoms': [{'units': 'Participants', 'counts': [{'value': '23', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.63', 'spread': '1.09', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 7', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '1.07', 'spread': '1.36', 'groupId': 'OG000'}]}]}, {'title': 'Dyspnoea, Survival Follow-Up Month 8', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}]}], 'categories': [{'measurements': [{'value': '0.10', 'spread': '0.14', 'groupId': 'OG000'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline up to approximately 30 months after first participant enrolled', 'description': "Change from baseline per SILC scale will be analyzed for each lung cancer symptoms scores. SILC questionnaire comprises 3 individual symptoms \\& are scored at individual symptom level, thus have a dyspnea score, chest pain score, \\& cough score. There are a total of 9 questions in SILC questionnaire, each question has a minimum value of 0 \\& maximum value of 4. Each individual symptom score is calculated as average of responses for symptom items. 'Chest pain' score is mean of question 1 \\& 2, 'Cough' score is mean of question 3 \\& 4 and 'Dyspnea' score is mean of question 5 to 9 in SILC questionnaire. An increase in score is suggestive of a worsening in symptomology. A score change of ≥0.3 points for dyspnea \\& cough symptom scores is considered to be clinically significant; whereas a score change of ≥0.5 points for chest pain score is considered to be clinically significant. (Note: PD=progression of disease)", 'unitOfMeasure': 'Units on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'PFS as Determined by the Investigator Using RECIST v1.1 in the ITT Population (Arm A and Arm B)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '343', 'groupId': 'OG000'}, {'value': '338', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG001', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '6.5', 'groupId': 'OG000', 'lowerLimit': '5.7', 'upperLimit': '7.1'}, {'value': '5.6', 'groupId': 'OG001', 'lowerLimit': '5.5', 'upperLimit': '6.9'}]}]}], 'analyses': [{'pValue': '0.4007', 'groupIds': ['OG000', 'OG001'], 'paramType': 'Hazard Ratio (HR)', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.930', 'ciLowerLimit': '0.784', 'ciUpperLimit': '1.102', 'statisticalMethod': 'Log Rank', 'nonInferiorityType': 'SUPERIORITY', 'nonInferiorityComment': 'Stratified Analysis'}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the ITT Population Arm A and Arm B.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'OS in the ITT Population (Arm A and Arm B)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '343', 'groupId': 'OG000'}, {'value': '338', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG001', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '14.2', 'groupId': 'OG000', 'lowerLimit': '12.3', 'upperLimit': '16.8'}, {'value': '12.6', 'groupId': 'OG001', 'lowerLimit': '11.6', 'upperLimit': '14.7'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the ITT Population, Arm A and Arm B.', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Intent To Treat (ITT) was defined as all randomized participants, irrespective of whether the assigned treatment was actually received.'}, {'type': 'SECONDARY', 'title': 'Percentage of Participants With Adverse Events', 'denoms': [{'units': 'Participants', 'counts': [{'value': '334', 'groupId': 'OG000'}, {'value': '334', 'groupId': 'OG001'}, {'value': '332', 'groupId': 'OG002'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'categories': [{'measurements': [{'value': '97.0', 'groupId': 'OG000'}, {'value': '99.4', 'groupId': 'OG001'}, {'value': '97.9', 'groupId': 'OG002'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to approximately 68 months after first participant enrolled', 'description': 'Percentage of participants with at least one adverse event.', 'unitOfMeasure': 'Percentage of participants', 'reportingStatus': 'POSTED', 'populationDescription': 'The safety population included all treated patients, defined as randomized patients who received any protocol treatment.'}, {'type': 'SECONDARY', 'title': 'Percentage of Participants With Anti-therapeutic Antibody (ATA) Response to Atezolizumab', 'denoms': [{'units': 'Participants', 'counts': [{'value': '338', 'groupId': 'OG000'}, {'value': '343', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Baseline evaluable participants', 'denoms': [{'units': 'Participants', 'counts': [{'value': '321', 'groupId': 'OG000'}, {'value': '320', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '3.1', 'groupId': 'OG000'}, {'value': '1.9', 'groupId': 'OG001'}]}]}, {'title': 'Post-baseline evaluable participants', 'denoms': [{'units': 'Participants', 'counts': [{'value': '308', 'groupId': 'OG000'}, {'value': '313', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '48.1', 'groupId': 'OG000'}, {'value': '21.4', 'groupId': 'OG001'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'Percentage of participants with Anti-therapeutic Antibody (ATA) response to atezolizumab.', 'unitOfMeasure': 'Percentage of participants', 'reportingStatus': 'POSTED', 'populationDescription': 'The baseline ADA evaluable population for each study treatment included participants who had a baseline ADA result. The post-baseline ADA evaluable population for each study treatment included participants who had at least one post baseline ADA result and who had received at least one dose of that study treatment.'}, {'type': 'SECONDARY', 'title': 'Maximum Observed Serum Atezolizumab Concentration (Cmax)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '327', 'groupId': 'OG000'}, {'value': '328', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Cycle 1 Day 1 Post dose', 'denoms': [{'units': 'Participants', 'counts': [{'value': '309', 'groupId': 'OG000'}, {'value': '302', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '372', 'spread': '116', 'groupId': 'OG000'}, {'value': '378', 'spread': '124', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 3 Day 1 Post dose', 'denoms': [{'units': 'Participants', 'counts': [{'value': '251', 'groupId': 'OG000'}, {'value': '263', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '470', 'spread': '147', 'groupId': 'OG000'}, {'value': '444', 'spread': '119', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Cycle 1 Day 1 and Cycle 3 Day 1 (Cycle length = 21 days)', 'description': 'Maximum observed serum atezolizumab concentration (Cmax). The predose samples will be collected on the same day of treatment administration. The infusion duration of atezolizumab will be of 30-60 minutes.', 'unitOfMeasure': 'µg/mL', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'The pharmacokinetic evaluable population is defined as all participants who received any dose of atezolizumab, carboplatin, paclitaxel, or nab paclitaxel and who had evaluable PK samples post-dose.'}, {'type': 'SECONDARY', 'title': 'Minimum Observed Serum Atezolizumab Concentration (Cmin)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '327', 'groupId': 'OG000'}, {'value': '328', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Cycle 1 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '311', 'groupId': 'OG000'}, {'value': '308', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': 'NA', 'spread': 'NA', 'comment': 'Below the level of detection.', 'groupId': 'OG000'}, {'value': 'NA', 'spread': 'NA', 'comment': 'Below the level of detection.', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 2 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '285', 'groupId': 'OG000'}, {'value': '289', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '63.9', 'spread': '29.9', 'groupId': 'OG000'}, {'value': '69.5', 'spread': '34.7', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 3 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '267', 'groupId': 'OG000'}, {'value': '281', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '103', 'spread': '40.1', 'groupId': 'OG000'}, {'value': '107', 'spread': '52.0', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 4 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '256', 'groupId': 'OG000'}, {'value': '252', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '128', 'spread': '62.3', 'groupId': 'OG000'}, {'value': '126', 'spread': '68.4', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 8 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '172', 'groupId': 'OG000'}, {'value': '180', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '188', 'spread': '80.4', 'groupId': 'OG000'}, {'value': '190', 'spread': '84.6', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 16 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '66', 'groupId': 'OG000'}, {'value': '78', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '201', 'spread': '79.2', 'groupId': 'OG000'}, {'value': '212', 'spread': '78.1', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 24 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '27', 'groupId': 'OG000'}, {'value': '30', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '187', 'spread': '90.4', 'groupId': 'OG000'}, {'value': '224', 'spread': '134', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 32 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '13', 'groupId': 'OG000'}, {'value': '9', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '242', 'spread': '88.4', 'groupId': 'OG000'}, {'value': '210', 'spread': '102', 'groupId': 'OG001'}]}]}, {'title': 'Cycle 40 Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '308', 'spread': '141', 'groupId': 'OG000'}, {'value': '174', 'spread': 'NA', 'comment': 'Not evaluable; only 1 participant.', 'groupId': 'OG001'}]}]}, {'title': 'Treatment Discontinuation Visit', 'denoms': [{'units': 'Participants', 'counts': [{'value': '133', 'groupId': 'OG000'}, {'value': '140', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '126', 'spread': '93.7', 'groupId': 'OG000'}, {'value': '137', 'spread': '103', 'groupId': 'OG001'}]}]}, {'title': 'Day 120 Post Last Dose', 'denoms': [{'units': 'Participants', 'counts': [{'value': '49', 'groupId': 'OG000'}, {'value': '62', 'groupId': 'OG001'}]}], 'categories': [{'measurements': [{'value': '7.81', 'spread': '9.76', 'groupId': 'OG000'}, {'value': '9.47', 'spread': '13.1', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Predose on Day 1 of Cycles 1-4, 8, 16, every 8 cycle thereafter (up to 30 months), at treatment discontinuation (up to 30 months), and at 120 days after the last dose of atezolizumab (up to approximately 30 months, each cycle is 21 days)', 'description': 'Minimum observed serum atezolizumab concentration (Cmin). The predose samples will be collected on the same day of treatment administration.', 'unitOfMeasure': 'µg/mL', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'The pharmacokinetic evaluable population is defined as all participants who received any dose of atezolizumab, carboplatin, paclitaxel, or nab paclitaxel and who had evaluable PK samples post-dose.'}, {'type': 'SECONDARY', 'title': 'Plasma Concentrations for Paclitaxel', 'denoms': [{'units': 'Participants', 'counts': [{'value': '35', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}], 'classes': [{'title': 'Cycle 1 Day 1 Prior to Infusion', 'denoms': [{'units': 'Participants', 'counts': [{'value': '32', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': 'NA', 'spread': 'NA', 'comment': 'Below the level of detection.', 'groupId': 'OG000'}]}]}, {'title': 'Cycle 1 Day 1 Before end of Infusion', 'denoms': [{'units': 'Participants', 'counts': [{'value': '30', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': '5860', 'spread': '2410', 'groupId': 'OG000'}]}]}, {'title': 'Cycle 1 Day 1 After Infusion', 'denoms': [{'units': 'Participants', 'counts': [{'value': '33', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': '2960', 'spread': '2770', 'groupId': 'OG000'}]}]}, {'title': 'Cycle 3 Day 1 Prior to Infusion', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': 'NA', 'spread': 'NA', 'comment': 'Below the threshold of the assay.', 'groupId': 'OG000'}]}]}, {'title': 'Cycle 3 Day 1 Before end of Infusion', 'denoms': [{'units': 'Participants', 'counts': [{'value': '23', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': '21900', 'spread': '42600', 'groupId': 'OG000'}]}]}, {'title': 'Cycle 3 Day 1 After Infusion', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': '11000', 'spread': '30700', 'groupId': 'OG000'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Prior to infusion (within same day of treatment administration), 5-10 minutes before the end of infusion, and 1 hour after the end of infusion (infusion duration 180 minutes) on Day 1 of Cycles 1 and 3 (each cycle is 21 days)', 'description': 'Plasma concentrations for paclitaxel.', 'unitOfMeasure': 'ng/mL', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'The pharmacokinetic evaluable population is defined as all participants who received any dose of atezolizumab, carboplatin, paclitaxel, or nab paclitaxel and who had evaluable PK samples post-dose.'}, {'type': 'SECONDARY', 'title': 'Plasma Concentrations for Nab-Paclitaxel', 'denoms': [{'units': 'Participants', 'counts': [{'value': '32', 'groupId': 'OG000'}, {'value': '38', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. 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Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. 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The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'OG002', 'title': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; carboplatin was administered on Day 1 of each 21-day cycle, nab-paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. 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The Day 1 order of drug administration was as follows: nab-paclitaxel, then carboplatin. Participants who experienced disease progression at any time during the induction phase discontinued all study treatment. In the maintenance phase, participants received best supportive care.'}, {'id': 'FG001', 'title': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab and carboplatin were administered on Day 1 of each 21-day cycle. Nab-Paclitaxel was administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. 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Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'BG002', 'title': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study consisted of four or six cycles; atezolizumab, paclitaxel, and carboplatin were administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration was as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experienced no further clinical benefit at any time during the induction phase discontinued all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants began maintenance therapy with atezolizumab. Atezolizumab was continued as long as there was clinical benefit to the participant.'}, {'id': 'BG003', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '64.9', 'spread': '8.1', 'groupId': 'BG000'}, {'value': '64.0', 'spread': '9.2', 'groupId': 'BG001'}, {'value': '65.0', 'spread': '8.3', 'groupId': 'BG002'}, {'value': '64.6', 'spread': '8.6', 'groupId': 'BG003'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'Years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '63', 'groupId': 'BG000'}, {'value': '63', 'groupId': 'BG001'}, {'value': '60', 'groupId': 'BG002'}, {'value': '186', 'groupId': 'BG003'}]}, {'title': 'Male', 'measurements': [{'value': '277', 'groupId': 'BG000'}, {'value': '280', 'groupId': 'BG001'}, {'value': '278', 'groupId': 'BG002'}, {'value': '835', 'groupId': 'BG003'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Ethnicity (NIH/OMB)', 'classes': [{'categories': [{'title': 'Hispanic or Latino', 'measurements': [{'value': '24', 'groupId': 'BG000'}, {'value': '27', 'groupId': 'BG001'}, {'value': '28', 'groupId': 'BG002'}, {'value': '79', 'groupId': 'BG003'}]}, {'title': 'Not Hispanic or Latino', 'measurements': [{'value': '299', 'groupId': 'BG000'}, {'value': '306', 'groupId': 'BG001'}, {'value': '297', 'groupId': 'BG002'}, {'value': '902', 'groupId': 'BG003'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '17', 'groupId': 'BG000'}, {'value': '10', 'groupId': 'BG001'}, {'value': '13', 'groupId': 'BG002'}, {'value': '40', 'groupId': 'BG003'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Race (NIH/OMB)', 'classes': [{'categories': [{'title': 'American Indian or Alaska Native', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '1', 'groupId': 'BG001'}, {'value': '3', 'groupId': 'BG002'}, {'value': '5', 'groupId': 'BG003'}]}, {'title': 'Asian', 'measurements': [{'value': '37', 'groupId': 'BG000'}, {'value': '41', 'groupId': 'BG001'}, {'value': '34', 'groupId': 'BG002'}, {'value': '112', 'groupId': 'BG003'}]}, {'title': 'Native Hawaiian or Other Pacific Islander', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}, {'value': '1', 'groupId': 'BG003'}]}, {'title': 'Black or African American', 'measurements': [{'value': '7', 'groupId': 'BG000'}, {'value': '4', 'groupId': 'BG001'}, {'value': '3', 'groupId': 'BG002'}, {'value': '14', 'groupId': 'BG003'}]}, {'title': 'White', 'measurements': [{'value': '290', 'groupId': 'BG000'}, {'value': '289', 'groupId': 'BG001'}, {'value': '290', 'groupId': 'BG002'}, {'value': '869', 'groupId': 'BG003'}]}, {'title': 'More than one race', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '6', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}, {'value': '8', 'groupId': 'BG003'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '4', 'groupId': 'BG000'}, {'value': '2', 'groupId': 'BG001'}, {'value': '6', 'groupId': 'BG002'}, {'value': '12', 'groupId': 'BG003'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}]}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2018-10-24', 'size': 3651648, 'label': 'Study Protocol', 'hasIcf': False, 'hasSap': False, 'filename': 'Prot_000.pdf', 'typeAbbrev': 'Prot', 'uploadDate': '2019-09-25T13:06', 'hasProtocol': True}, {'date': '2018-01-11', 'size': 921776, 'label': 'Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'SAP_001.pdf', 'typeAbbrev': 'SAP', 'uploadDate': '2019-09-25T13:06', 'hasProtocol': False}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 1021}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2015-06-11', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-03', 'completionDateStruct': {'date': '2021-02-17', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2022-03-17', 'studyFirstSubmitDate': '2015-02-13', 'resultsFirstSubmitDate': '2019-09-25', 'studyFirstSubmitQcDate': '2015-02-13', 'lastUpdatePostDateStruct': {'date': '2022-03-21', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2019-10-21', 'studyFirstPostDateStruct': {'date': '2015-02-20', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2019-11-12', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2018-10-03', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Progression Free Survival (PFS) as Determined by the Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in the Intent-to-Treat (ITT) Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the ITT population.'}, {'measure': 'Overall Survival (OS) in the ITT Population', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the ITT population.'}], 'secondaryOutcomes': [{'measure': 'OS in the in the Teff Population', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the in the Teff Population.'}, {'measure': 'PFS as Determined by the Investigator Using RECIST v1.1 in the Teff Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the Teff Population.'}, {'measure': 'PFS as Determined by the Investigator Using RECIST v1.1 in the Tumor Cell (TC) 2/3 or Tumor-Infiltrating Immune Cell (IC) 2/3 Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the Tumor Cell (TC) 2/3 or Tumor-Infiltrating Immune Cell (IC) 2/3 Population.'}, {'measure': 'PFS as Determined by the Investigator Using RECIST v1.1 in the TC1/2/3 or IC1/2/3 Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the TC1/2/3 or IC1/2/3 Population.'}, {'measure': 'OS in the TC2/3 or IC2/3 Population', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause, in the TC2/3 or IC2/3 Population.'}, {'measure': 'OS in the TC1/2/3 or IC1/2/3 Population', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the TC1/2/3 or IC1/2/3 Population.'}, {'measure': 'Percentage of Participants With Objective Response as Determined by the Investigator Using RECIST v1.1 in the ITT Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'Proportion of participants with an objective response (CR or PR) in the ITT population.'}, {'measure': 'Duration of Response as Determined by the Investigator Using RECIST v1.1 in the ITT Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'Duration of response is defined as the time from the first documented objective response to documented PD or death from any cause, whichever occurred first, in the ITT Population.'}, {'measure': 'Event Free Rate at 1 and 2 Years in the ITT Population', 'timeFrame': '1 and 2 years', 'description': 'Event free rate at 1 and 2 years is defined as the proportion of participants alive at 1 and 2 years after randomization estimated using Kaplan-Meier (KM) methodology for the ITT population.'}, {'measure': 'Time to Deterioration (TTD) in Patient-reported Lung Cancer Symptoms Using EORTC QLQ-C30 Symptom Subscales in the ITT Population', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'TTD in Patient-reported Lung Cancer Symptoms Using EORTC QLQ-C30 Symptom Subscales in the ITT Population. The EORTC QLQ-C30 is a validated and reliable self-report measure that consists of 30 questions that assess five aspects of patient functioning (physical, emotional, role, cognitive, and social), three symptom scales (fatigue, nausea and vomiting, pain), global health/quality of life, and six single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). EORTC scales and single-item measures will be linearly transformed so that each score has a range of 0-100. A high score for a functional scale represents a high or healthy level of functioning, and a high score for the global health status and HRQoL represents a high HRQoL; however, a high score for a symptom scale or item represents a high level of symptomatology or problems.'}, {'measure': 'TTD in Patient-reported Lung Cancer Symptoms Using EORTC QLQ-LC13 Symptom Subscales in the ITT Population', 'timeFrame': 'Up to approximately 30 months after the first participant enrolled', 'description': 'TTD was documented for a 3-symptom composite endpoint using the following EORTC QLQ-LC13 symptom scores: cough, chest pain, and dyspnea multi--item scale. In this instance, symptom deterioration will be determined as a \\>= 10-point increase above baseline in any of the listed symptom scores, whichever occurs first (cough, chest pain, and dyspnea multi-item scale). Confirmed clinically meaningful symptom deterioration will need to be held for the original symptom; a \\>= 10-point increase above baseline in a symptom score must be held for at least two consecutive assessments or an initial\\>=10-point increase above baseline followed by death within 3 weeks from the last assessment. A \\>= 10-point change in the EORTC scale score is perceived by patients as clinically significant.'}, {'measure': 'Change From Baseline in Patient-reported Lung Cancer Symptoms Score Using the SILC Scale Symptom Severity Score in the ITT Population', 'timeFrame': 'Baseline up to approximately 30 months after first participant enrolled', 'description': "Change from baseline per SILC scale will be analyzed for each lung cancer symptoms scores. SILC questionnaire comprises 3 individual symptoms \\& are scored at individual symptom level, thus have a dyspnea score, chest pain score, \\& cough score. There are a total of 9 questions in SILC questionnaire, each question has a minimum value of 0 \\& maximum value of 4. Each individual symptom score is calculated as average of responses for symptom items. 'Chest pain' score is mean of question 1 \\& 2, 'Cough' score is mean of question 3 \\& 4 and 'Dyspnea' score is mean of question 5 to 9 in SILC questionnaire. An increase in score is suggestive of a worsening in symptomology. A score change of ≥0.3 points for dyspnea \\& cough symptom scores is considered to be clinically significant; whereas a score change of ≥0.5 points for chest pain score is considered to be clinically significant. (Note: PD=progression of disease)"}, {'measure': 'PFS as Determined by the Investigator Using RECIST v1.1 in the ITT Population (Arm A and Arm B)', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'PFS is defined as the time between the date of randomization and the date of first documented disease progression or death, whichever occurs first, in the ITT Population Arm A and Arm B.'}, {'measure': 'OS in the ITT Population (Arm A and Arm B)', 'timeFrame': 'Up to approximately 39 months after first participant enrolled', 'description': 'OS is defined as the time between the date of randomization and date of death from any cause in the ITT Population, Arm A and Arm B.'}, {'measure': 'Percentage of Participants With Adverse Events', 'timeFrame': 'Up to approximately 68 months after first participant enrolled', 'description': 'Percentage of participants with at least one adverse event.'}, {'measure': 'Percentage of Participants With Anti-therapeutic Antibody (ATA) Response to Atezolizumab', 'timeFrame': 'Up to approximately 30 months after first participant enrolled', 'description': 'Percentage of participants with Anti-therapeutic Antibody (ATA) response to atezolizumab.'}, {'measure': 'Maximum Observed Serum Atezolizumab Concentration (Cmax)', 'timeFrame': 'Cycle 1 Day 1 and Cycle 3 Day 1 (Cycle length = 21 days)', 'description': 'Maximum observed serum atezolizumab concentration (Cmax). The predose samples will be collected on the same day of treatment administration. The infusion duration of atezolizumab will be of 30-60 minutes.'}, {'measure': 'Minimum Observed Serum Atezolizumab Concentration (Cmin)', 'timeFrame': 'Predose on Day 1 of Cycles 1-4, 8, 16, every 8 cycle thereafter (up to 30 months), at treatment discontinuation (up to 30 months), and at 120 days after the last dose of atezolizumab (up to approximately 30 months, each cycle is 21 days)', 'description': 'Minimum observed serum atezolizumab concentration (Cmin). The predose samples will be collected on the same day of treatment administration.'}, {'measure': 'Plasma Concentrations for Paclitaxel', 'timeFrame': 'Prior to infusion (within same day of treatment administration), 5-10 minutes before the end of infusion, and 1 hour after the end of infusion (infusion duration 180 minutes) on Day 1 of Cycles 1 and 3 (each cycle is 21 days)', 'description': 'Plasma concentrations for paclitaxel.'}, {'measure': 'Plasma Concentrations for Nab-Paclitaxel', 'timeFrame': 'Prior to infusion (within same day of treatment administration), 5-10 minutes before the end of infusion, and 1 hour after the end of infusion (infusion duration 30 minutes) on Day 1 of Cycles 1 and 3 (each cycle is 21 days)', 'description': 'Plasma concentrations for nab-paclitaxel.'}, {'measure': 'Plasma Concentrations for Carboplatin', 'timeFrame': 'Prior to infusion (within same day of treatment administration), 5-10 minutes before the end of infusion, and 1 hour after the end of infusion (infusion duration 15 to 30 minutes) on Day 1 of Cycles 1 and 3 (each cycle is 21 days)', 'description': 'Plasma concentrations for carboplatin.'}]}, 'conditionsModule': {'conditions': ['Squamous Non-Small Cell Lung Cancer']}, 'referencesModule': {'references': [{'pmid': '35511917', 'type': 'DERIVED', 'citation': 'Ton TGN, Pal N, Trinh H, Mahrus S, Bretscher MT, Machado RJM, Sadetsky N, Chaudhary N, Lu MW, Riely GJ. Replication of Overall Survival, Progression-Free Survival, and Overall Response in Chemotherapy Arms of Non-Small Cell Lung Cancer Trials Using Real-World Data. Clin Cancer Res. 2022 Jul 1;28(13):2844-2853. doi: 10.1158/1078-0432.CCR-22-0471.'}]}, 'descriptionModule': {'briefSummary': 'This randomized, open-label study will evaluate the safety and efficacy of atezolizumab (MPDL3280A) in combination with carboplatin + paclitaxel or carboplatin + nab-paclitaxel compared with treatment with carboplatin + nab-paclitaxel in chemotherapy-naive participants with Stage IV squamous NSCLC.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1\n* Histologically or cytologically confirmed, treatment-naïve Stage IV squamous NSCLC\n* Previously obtained archival tumor tissue or tissue obtained from biopsy at screening\n* Measurable disease as defined by RECIST v1.1\n* Adequate hematologic and end organ function\n\nExclusion Criteria:\n\n* Active or untreated central nervous system (CNS) metastasis\n* Malignancies other than NSCLC within 5 years prior to randomization, with the exception of those with a negligible risk of metastasis or death treated with expected curative outcome\n* Pregnant or lactating women\n* History of autoimmune disease\n* History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest Computed Tomography (CT) scan, History of radiation pneumonitis in the radiation field (fibrosis) is permitted\n* Positive test for Human Immunodeficiency Virus (HIV)\n* Active hepatitis B or hepatitis C\n* Prior treatment with cluster of differentiation 137 (CD137) agonists or immune checkpoint blockade therapies, anti-programmed death-1 (anti-PD-1), and anti-PD-L1 therapeutic antibody\n* Severe infection within 4 weeks prior to randomization\n* Significant history of cardiovascular disease'}, 'identificationModule': {'nctId': 'NCT02367794', 'briefTitle': 'A Study of Atezolizumab in Combination With Carboplatin + Paclitaxel or Carboplatin + Nab-Paclitaxel Compared With Carboplatin + Nab-Paclitaxel in Participants With Stage IV Squamous Non-Small Cell Lung Cancer (NSCLC) [IMpower131]', 'organization': {'class': 'INDUSTRY', 'fullName': 'Hoffmann-La Roche'}, 'officialTitle': 'A Phase III, Open-Label, Multicenter, Randomized Study Evaluating the Efficacy and Safety of Atezolizumab (MPDL3280A, Anti-PD-L1 Antibody) in Combination With Carboplatin+Paclitaxel or Atezolizumab in Combination With Carboplatin+Nab-Paclitaxel Versus Carboplatin+Nab-Paclitaxel in Chemotherapy-Naive Patients With Stage IV Squamous Non-Small Cell Lung Cancer', 'orgStudyIdInfo': {'id': 'GO29437'}, 'secondaryIdInfos': [{'id': '2014-003208-59', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'description': 'The induction phase of the study will consist of four or six cycles; atezolizumab, paclitaxel, and carboplatin will be administered on Day 1 of each 21-day cycle. The Day 1 order of drug administration is as follows: atezolizumab, then paclitaxel, then carboplatin. Participants who experience no further clinical benefit at any time during the induction phase will discontinue all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants will begin maintenance therapy with atezolizumab. Atezolizumab will be continued as long as there is a clinical benefit to the participant.', 'interventionNames': ['Drug: Atezolizumab (MPDL3280A), an engineered anti-programmed death-ligand 1 (anti-PD-L1) antibody', 'Drug: Carboplatin', 'Drug: Paclitaxel']}, {'type': 'EXPERIMENTAL', 'label': 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study will consist of four or six cycles; atezolizumab and carboplatin will be administered on Day 1 of each 21-day cycle. Nab-Paclitaxel will be administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration is as follows: atezolizumab, then nab-paclitaxel, then carboplatin. Participants who experience no further clinical benefit at any time during the induction phase will discontinue all study treatments. In the absence of the above criteria, after the 4- or 6-cycle induction phase, participants will begin maintenance therapy with atezolizumab. Atezolizumab will be continued as long as there is a clinical benefit to the participant.', 'interventionNames': ['Drug: Atezolizumab (MPDL3280A), an engineered anti-programmed death-ligand 1 (anti-PD-L1) antibody', 'Drug: Carboplatin', 'Drug: Nab-Paclitaxel']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Arm C: Nab-Paclitaxel + Carboplatin', 'description': 'The induction phase of the study will consist of four or six cycles; carboplatin will be administered on Day 1 of each 21-day cycle, nab-paclitaxel will be administered on Days 1, 8, and 15 of each 21-day cycle. The Day 1 order of drug administration is as follows: nab-paclitaxel, then carboplatin. Participants who experience disease progression at any time during the induction phase will discontinue all study treatment. In the maintenance phase, participants will receive best supportive care.', 'interventionNames': ['Drug: Carboplatin', 'Drug: Nab-Paclitaxel']}], 'interventions': [{'name': 'Atezolizumab (MPDL3280A), an engineered anti-programmed death-ligand 1 (anti-PD-L1) antibody', 'type': 'DRUG', 'otherNames': ['Tecentriq'], 'description': 'Atezolizumab 1200 milligrams (mg) intravenous infusion (IV) on day 1 of each 21-day cycle.', 'armGroupLabels': ['Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin']}, {'name': 'Carboplatin', 'type': 'DRUG', 'description': 'Carboplatin area under the concentration curve (AUC) 6 milligrams per milliliter per minute (mg/mL/min) on Day 1 of each 21-day cycle for 4 or 6 cycles.', 'armGroupLabels': ['Arm A: Atezolizumab + Paclitaxel + Carboplatin', 'Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'Arm C: Nab-Paclitaxel + Carboplatin']}, {'name': 'Nab-Paclitaxel', 'type': 'DRUG', 'description': 'Nab-paclitaxel 100 milligrams per meter squared (mg/m\\^2) IV on Day 1, 8, and 15 of each 21-day cycle for 4 or 6 cycles.', 'armGroupLabels': ['Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin', 'Arm C: Nab-Paclitaxel + Carboplatin']}, {'name': 'Paclitaxel', 'type': 'DRUG', 'description': 'Paclitaxel 200 mg/m\\^2 IV on Day 1 of each 21-day cycle for 4 or 6 cycles. Participants of Asian race/ethnicity will be administered paclitaxel 175 mg/m\\^2 IV.', 'armGroupLabels': ['Arm A: Atezolizumab + Paclitaxel + Carboplatin']}]}, 'contactsLocationsModule': {'locations': [{'zip': '85224', 'city': 'Chandler', 'state': 'Arizona', 'country': 'United States', 'facility': 'Ironwood Cancer & Research Centers', 'geoPoint': {'lat': 33.30616, 'lon': -111.84125}}, {'zip': '72762', 'city': 'Springdale', 'state': 'Arkansas', 'country': 'United States', 'facility': 'Highlands Oncology Group', 'geoPoint': {'lat': 36.18674, 'lon': -94.12881}}, {'city': 'Bellflower', 'state': 'California', 'country': 'United States', 'facility': 'Southern CA Permanente Med Grp', 'geoPoint': {'lat': 33.88168, 'lon': -118.11701}}, {'zip': '94611', 'city': 'Oakland', 'state': 'California', 'country': 'United States', 'facility': 'Kaiser Permanente Oakland Medical Center', 'geoPoint': {'lat': 37.80437, 'lon': -122.2708}}, {'zip': '95825', 'city': 'Sacramento', 'state': 'California', 'country': 'United States', 'facility': 'Kaiser Permanente - Sacramento Medical Center and Medical Offices', 'geoPoint': {'lat': 38.58157, 'lon': -121.4944}}, {'zip': '94577', 'city': 'San Leandro', 'state': 'California', 'country': 'United States', 'facility': 'Kaiser Permanente - San Leandro Medical Center', 'geoPoint': {'lat': 37.72493, 'lon': -122.15608}}, {'zip': '95051', 'city': 'Santa Clara', 'state': 'California', 'country': 'United States', 'facility': 'Kaiser Permanente - Santa Clara', 'geoPoint': {'lat': 37.35411, 'lon': -121.95524}}, {'zip': '94589', 'city': 'Vallejo', 'state': 'California', 'country': 'United States', 'facility': 'Kaiser Permanente; Oncology Clinical Trials', 'geoPoint': {'lat': 38.10409, 'lon': -122.25664}}, {'zip': '94596', 'city': 'Walnut Creek', 'state': 'California', 'country': 'United States', 'facility': 'Kaiser Permanente - Walnut Creek', 'geoPoint': {'lat': 37.90631, 'lon': -122.06496}}, {'zip': '80218', 'city': 'Denver', 'state': 'Colorado', 'country': 'United States', 'facility': 'Rocky Mountain Cancer Center', 'geoPoint': {'lat': 39.73915, 'lon': -104.9847}}, {'zip': '06810', 'city': 'Danbury', 'state': 'Connecticut', 'country': 'United States', 'facility': 'Danbury Hospital', 'geoPoint': {'lat': 41.39482, 'lon': -73.45401}}, {'zip': '33308', 'city': 'Fort Lauderdale', 'state': 'Florida', 'country': 'United States', 'facility': 'Holy Cross Hospital Inc', 'geoPoint': {'lat': 26.12231, 'lon': -80.14338}}, {'zip': '33916', 'city': 'Fort Myers', 'state': 'Florida', 'country': 'United States', 'facility': 'SCRI Florida Cancer Specialists South', 'geoPoint': {'lat': 26.62168, 'lon': -81.84059}}, {'zip': '33410', 'city': 'Palm Beach Gardens', 'state': 'Florida', 'country': 'United States', 'facility': 'Florida Cancer Specialists', 'geoPoint': {'lat': 26.82339, 'lon': -80.13865}}, {'zip': '34952', 'city': 'Port Saint Lucie', 'state': 'Florida', 'country': 'United States', 'facility': 'Hematology Oncology Associates of the Treasure Coast', 'geoPoint': {'lat': 27.29393, 'lon': -80.35033}}, {'zip': '33705', 'city': 'St. Petersburg', 'state': 'Florida', 'country': 'United States', 'facility': "Florida Cancer Specialists (St. Petersburg - St. Anthony's Professional Building)", 'geoPoint': {'lat': 27.77086, 'lon': -82.67927}}, {'zip': '30607', 'city': 'Athens', 'state': 'Georgia', 'country': 'United States', 'facility': 'University Cancer & Blood Center, LLC; Research', 'geoPoint': {'lat': 33.96095, 'lon': -83.37794}}, {'zip': '30117', 'city': 'Carrollton', 'state': 'Georgia', 'country': 'United States', 'facility': 'Northwest Georgia Oncology Centers, a Service of Wellstar Cobb Hospital', 'geoPoint': {'lat': 33.58011, 'lon': -85.07661}}, {'zip': '31201', 'city': 'Macon', 'state': 'Georgia', 'country': 'United States', 'facility': 'Central Georgia Cancer Care PC', 'geoPoint': {'lat': 32.84069, 'lon': -83.6324}}, {'zip': '30265', 'city': 'Newnan', 'state': 'Georgia', 'country': 'United States', 'facility': 'Southeastern Regional Medical Center, Inc.', 'geoPoint': {'lat': 33.38067, 'lon': -84.79966}}, {'zip': '60637', 'city': 'Chicago', 'state': 'Illinois', 'country': 'United States', 'facility': 'University of Chicago', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '60435', 'city': 'Joliet', 'state': 'Illinois', 'country': 'United States', 'facility': 'Joliet Oncology-Hematology; Associates, Ltd.', 'geoPoint': {'lat': 41.52519, 'lon': -88.0834}}, {'zip': '62301', 'city': 'Quincy', 'state': 'Illinois', 'country': 'United States', 'facility': 'Quincy Medical Group', 'geoPoint': {'lat': 39.9356, 'lon': -91.40987}}, {'zip': '46845', 'city': 'Fort Wayne', 'state': 'Indiana', 'country': 'United States', 'facility': 'Fort Wayne Med Oncology & Hematology Inc', 'geoPoint': {'lat': 41.1306, 'lon': -85.12886}}, {'zip': '52722', 'city': 'Bettendorf', 'state': 'Iowa', 'country': 'United States', 'facility': 'Hematology-Oncology; Associates of the Quad Cities', 'geoPoint': {'lat': 41.52448, 'lon': -90.51569}}, {'zip': '51101', 'city': 'Sioux City', 'state': 'Iowa', 'country': 'United States', 'facility': 'Siouxland Hematology/Oncology', 'geoPoint': {'lat': 42.49999, 'lon': -96.40031}}, {'zip': '02421', 'city': 'Lexington', 'state': 'Kentucky', 'country': 'United States', 'facility': 'Lahey Clinic Med Ctr', 'geoPoint': {'lat': 37.98869, 'lon': -84.47772}}, {'zip': '40202', 'city': 'Louisville', 'state': 'Kentucky', 'country': 'United States', 'facility': 'Norton Cancer Institute', 'geoPoint': {'lat': 38.25424, 'lon': -85.75941}}, {'zip': '70121', 'city': 'New Orleans', 'state': 'Louisiana', 'country': 'United States', 'facility': 'Ochsner Clinic Foundation', 'geoPoint': {'lat': 29.95465, 'lon': -90.07507}}, {'zip': '04074', 'city': 'Scarborough', 'state': 'Maine', 'country': 'United States', 'facility': 'New England Cancer Specialists', 'geoPoint': {'lat': 43.57814, 'lon': -70.32172}}, {'zip': '02719', 'city': 'Fairhaven', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Southcoast Health System; Southcoast Centers For Cancer Care', 'geoPoint': {'lat': 41.6376, 'lon': -70.90365}}, {'zip': '48106', 'city': 'Ann Arbor', 'state': 'Michigan', 'country': 'United States', 'facility': 'St. Joseph Mercy Health System', 'geoPoint': {'lat': 42.27756, 'lon': -83.74088}}, {'zip': '48201', 'city': 'Detroit', 'state': 'Michigan', 'country': 'United States', 'facility': 'Karmanos Cancer Institute', 'geoPoint': {'lat': 42.33143, 'lon': -83.04575}}, {'zip': '55805', 'city': 'Duluth', 'state': 'Minnesota', 'country': 'United States', 'facility': "St. Luke's Regional Cancer Center", 'geoPoint': {'lat': 46.78327, 'lon': -92.10658}}, {'zip': '38801', 'city': 'Tupelo', 'state': 'Mississippi', 'country': 'United States', 'facility': 'Hematology and Oncology Associates at Bridgepoint', 'geoPoint': {'lat': 34.25807, 'lon': -88.70464}}, {'zip': '59102', 'city': 'Billings', 'state': 'Montana', 'country': 'United States', 'facility': 'Billings Clinic', 'geoPoint': {'lat': 45.78329, 'lon': -108.50069}}, {'zip': '07652', 'city': 'Paramus', 'state': 'New Jersey', 'country': 'United States', 'facility': 'Valley Hospital; 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