Ignite Creation Date:
2025-12-24 @ 11:25 PM
Ignite Modification Date:
2026-02-23 @ 12:22 PM
Study NCT ID:
NCT06426056
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-05-23
First Post:
2024-05-17
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Nab-Paclitaxel Plus Cisplatin With Concurrent Radiotherapy for Patients With Locally Advanced Cervical Cancer: A Multicentre, Single-arm, Phase II Trial.
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D002583', 'term': 'Uterine Cervical Neoplasms'}], 'ancestors': [{'id': 'D014594', 'term': 'Uterine Neoplasms'}, {'id': 'D005833', 'term': 'Genital Neoplasms, Female'}, {'id': 'D014565', 'term': 'Urogenital Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D002577', 'term': 'Uterine Cervical Diseases'}, {'id': 'D014591', 'term': 'Uterine Diseases'}, {'id': 'D005831', 'term': 'Genital Diseases, Female'}, {'id': 'D052776', 'term': 'Female Urogenital Diseases'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D000091662', 'term': 'Genital Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D011878', 'term': 'Radiotherapy'}, {'id': 'D013660', 'term': 'Taxes'}, {'id': 'D017239', 'term': 'Paclitaxel'}, {'id': 'D007267', 'term': 'Injections'}, {'id': 'D002945', 'term': 'Cisplatin'}], 'ancestors': [{'id': 'D013812', 'term': 'Therapeutics'}, {'id': 'D004467', 'term': 'Economics'}, {'id': 'D004472', 'term': 'Health Care Economics and Organizations'}, {'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': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D004224', 'term': 'Diterpenes'}, {'id': 'D013729', 'term': 'Terpenes'}, {'id': 'D004333', 'term': 'Drug Administration Routes'}, {'id': 'D004358', 'term': 'Drug Therapy'}, {'id': 'D017606', 'term': 'Chlorine Compounds'}, {'id': 'D007287', 'term': 'Inorganic Chemicals'}, {'id': 'D017672', 'term': 'Nitrogen Compounds'}, {'id': 'D017671', 'term': 'Platinum Compounds'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP', 'interventionModelDescription': 'Radiation Therapy Concurrently With Nab-Paclitaxel Plus Cisplatin'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 64}}, 'statusModule': {'overallStatus': 'NOT_YET_RECRUITING', 'startDateStruct': {'date': '2024-06', 'type': 'ESTIMATED'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2024-04', 'completionDateStruct': {'date': '2028-10', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2024-05-17', 'studyFirstSubmitDate': '2024-05-17', 'studyFirstSubmitQcDate': '2024-05-17', 'lastUpdatePostDateStruct': {'date': '2024-05-23', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2024-05-23', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-09', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'ORR (objective response rate)', 'timeFrame': 'the 1, 3, 6, 9, 12 months after the end of the treatment', 'description': 'ORR(objective response rate)=CR (complete response)+PR(partial response)/all participants'}], 'secondaryOutcomes': [{'measure': 'AE', 'timeFrame': 'the 1, 3, 6, 9, 12 months, and 2, 3 years after the end of the treatment', 'description': 'adverse events'}, {'measure': 'OS', 'timeFrame': 'the 1, 2, and 3 years after the end of the treatment', 'description': 'objective response rate'}, {'measure': 'PFS', 'timeFrame': 'the 1, 2, and 3 years after the end of the treatment', 'description': 'progression-free survival'}, {'measure': 'DOR', 'timeFrame': 'the 1, 3, 6, 9, 12 months, and 2, 3 years after the end of the treatment', 'description': 'duration of response'}, {'measure': 'DCR', 'timeFrame': 'the 1, 3, 6, 9, 12 months, and 2, 3 years after the end of the treatment', 'description': 'disease control rate'}, {'measure': 'CBR', 'timeFrame': 'the 1, 3, 6, 9, 12 months, and 2, 3 years after the end of the treatment', 'description': 'clinical benefit rate'}]}, 'oversightModule': {'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Cervical Cancer']}, 'descriptionModule': {'briefSummary': 'Based on the Phase I trial completed by the sponsor, the Phase II clinical trial aims to investigate the effectiveness and safety of image guidance volume-modulated arc radiation therapy concurrently with Nab-Paclitaxel plus Cisplatin for patients with locally advanced cervical cancer.'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '75 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* (1) Stage IB3 to IVA disease based on the 2018 International Federation of Gynecology and Obstetrics (FIGO) system;\n* (2) Eastern Cooperative Oncology Group at 2 or less;\n* (3) Life expectancy of greater than 3 months;\n* (4) Left ventricular ejection fraction at ≥55%;\n* (5) Neutrophil count at ≥1500/mm\\^3, platelet count at ≥100,000/mm\\^3 or hemoglobin at ≥9.0 g/dL;\n* (6) Serum creatinine at \\<1.5 times the upper limit of the normal reference range;\n* (7) Alanine transaminase or aspartate aminotransferase at \\>2.5 times the upper limit of the normal reference range;\n* (8) Non pregnant or lactating women;\n* (9) Women of childbearing age willing to adopt reliable contraceptive measures;\n* (10) Sign informed consent form.\n\nExclusion Criteria:\n\n* (1) Individuals who have previously received chemotherapy with albumin bound paclitaxel;\n* (2) Individuals who have previously received abdominal or pelvic radiation therapy;\n* (3) Individuals who have received neoadjuvant chemotherapy or targeted, immunotherapy, and other anti-tumor treatments prior to concurrent chemoradiotherapy and chemotherapy;\n* (4) Individuals with central nervous system diseases or brain metastases；\n* (5) Other malignant tumors other than cervical cancer have appeared within the past 5 years;\n* (6) Previously experienced sensory or motor neuropathy (Grade ≥ 2) ;\n* (7) The researchers evaluate that the uncontrolled serious medical diseases that will affect the ability of the participants to receive the treatment of the clinical trial, such as complicated with serious medical diseases, including serious heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hypertension, uncontrolled infection, active peptic ulcer, etc;\n* (8) known to be allergic to paclitaxel;\n* (9) Received other experimental drugs or participated in clinical studies for other anti-cancer treatment purposes within 30 days of the first chemotherapy administration;\n* (10) Serious infections occurring within 4 weeks prior to the start of research treatment, including but not limited to complications of infection requiring hospitalization, bacteremia, or severe pneumonia;\n* (11) Human immunodeficiency virus (HIV) positive individuals;\n* (12) Uncontrolled or active viral hepatitis or infection with human immunodeficiency virus;\n* (13) Researchers determine that it is not suitable to participate in this study.'}, 'identificationModule': {'nctId': 'NCT06426056', 'briefTitle': 'Nab-Paclitaxel Plus Cisplatin With Concurrent Radiotherapy for Patients With Locally Advanced Cervical Cancer: A Multicentre, Single-arm, Phase II Trial.', 'organization': {'class': 'OTHER', 'fullName': 'Peking University Third Hospital'}, 'officialTitle': 'Nab-Paclitaxel Plus Cisplatin With Concurrent Radiotherapy for Patients With Locally Advanced Cervical Cancer:A Multicentre, Single-arm, Phase II Trial.', 'orgStudyIdInfo': {'id': 'M2024240'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Experimental group', 'description': 'Image guidance volume modulated arc therapy included 50.4 Gy in 28 fractions to the pelvis and 59.4 Gy simultaneous boost in 28 fractions to involved pelvic and para-aortic lymph nodes, and subsequent high-dose-rate intracavitary brachytherapy at a total dose of 30.0-36.0 Gy in 5-6 fractions, twice a week. Concurrent chemotherapy regimen included weekly cisplatin (40 mg/m\\^2) and weekly nab-paclitaxel at escalating doses (33 mg/m\\^2 per week).', 'interventionNames': ['Radiation: radiotherapy', 'Drug: Nab paclitaxel', 'Drug: Cisplatin']}], 'interventions': [{'name': 'radiotherapy', 'type': 'RADIATION', 'otherNames': ['RT'], 'description': 'Image guidance volume modulated arc therapy included 50.4 Gy in 28 fractions to the pelvis and 59.4 Gy simultaneous boost in 28 fractions to involved pelvic and para-aortic lymph nodes, and subsequent high-dose-rate intracavitary brachytherapy at a total dose of 30.0-36.0 Gy in 5-6 fractions, twice a week.', 'armGroupLabels': ['Experimental group']}, {'name': 'Nab paclitaxel', 'type': 'DRUG', 'otherNames': ['paclitaxel for injection (albumin bound)'], 'description': 'Concurrent chemotherapy regimen included weekly cisplatin (40 mg/m\\^2) and weekly nab-paclitaxel at escalating doses (33 mg/m\\^2 per week).', 'armGroupLabels': ['Experimental group']}, {'name': 'Cisplatin', 'type': 'DRUG', 'description': 'Concurrent chemotherapy regimen included weekly cisplatin (40 mg/m\\^2) and weekly nab-paclitaxel at escalating doses (33 mg/m\\^2 per week).', 'armGroupLabels': ['Experimental group']}]}, 'contactsLocationsModule': {'centralContacts': [{'name': 'Ping Jiang, doctor', 'role': 'CONTACT', 'email': 'jiangping@bjmu.edu.cn', 'phone': '86010-82266699'}], 'overallOfficials': [{'name': 'Ping Jiang, Doctor', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Peking University Third Hospital'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Peking University Third Hospital', 'class': 'OTHER'}, 'collaborators': [{'name': 'Jilin Provincial Tumor Hospital', 'class': 'OTHER'}, {'name': 'Affiliated Hospital of Hebei University', 'class': 'OTHER'}, {'name': 'Hebei Medical University Fourth Hospital', 'class': 'OTHER'}], 'responsibleParty': {'type': 'SPONSOR'}}}}