Ignite Creation Date:
2025-12-25 @ 2:51 AM
Ignite Modification Date:
2025-12-31 @ 11:37 PM
Study NCT ID:
NCT07110233
Status:
NOT_YET_RECRUITING
Last Update Posted:
2025-08-07
First Post:
2025-07-31
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Yttrium-90 Radiation Segmentectomy for Hepatocellular Carcinoma
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006528', 'term': 'Carcinoma, Hepatocellular'}, {'id': 'D008113', 'term': 'Liver Neoplasms'}], 'ancestors': [{'id': 'D000230', 'term': 'Adenocarcinoma'}, {'id': 'D002277', 'term': 'Carcinoma'}, {'id': 'D009375', 'term': 'Neoplasms, Glandular and Epithelial'}, {'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D004067', 'term': 'Digestive System Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D004066', 'term': 'Digestive System Diseases'}, {'id': 'D008107', 'term': 'Liver Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'DIAGNOSTIC', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 64}}, 'statusModule': {'overallStatus': 'NOT_YET_RECRUITING', 'startDateStruct': {'date': '2025-11-01', 'type': 'ESTIMATED'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-07', 'completionDateStruct': {'date': '2028-05-31', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-07-31', 'studyFirstSubmitDate': '2025-07-31', 'studyFirstSubmitQcDate': '2025-07-31', 'lastUpdatePostDateStruct': {'date': '2025-08-07', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2025-08-07', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2028-05-31', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Objective Response Rate (ORR) by mRECIST', 'timeFrame': 'Up to 6 months', 'description': 'The objective response rate (ORR) after radiation segmentectomy in participants will be evaluated using a modified Response Evaluation Criteria in Solid Tumors (mRECIST) based on the best tumor response where Complete Response (CR) is defined as the disappearance of any intratumoral arterial enhancement in all target lesions, Partial Response (PR) is defined as a 30% decrease in the sum of diameters of viable (enhancement in the arterial phase) target lesions, taking as reference the baseline sum of the diameters of target lesions, Stable Disease (SD) is defined as any cases that do not qualify for either partial response or progressive disease, and Progressive Disease (PD) is defined as an increase of at least 20% in the sum of the diameters of viable (enhancing) target lesions, taking as reference the smallest sum of the diameters of viable (enhancing) target lesions recorded since treatment started.'}, {'measure': 'Percentage of participants with treatment-related adverse events', 'timeFrame': 'Up to 6 months', 'description': 'The percentage of participants with grade 3 or greater, treatment-related adverse events as classified by NCI Common Terminology Criteria for Adverse Events (CTCAE) will be reported.'}], 'secondaryOutcomes': [{'measure': 'Median time from TheraSphere administration to transplant', 'timeFrame': 'Up to 3 years', 'description': 'Transplant-free survival is defined as the time to transplant in months from TheraSphere administration until transplant or death by any cause using the Kaplan-Meier estimator and 90% confidence intervals.'}, {'measure': 'Median time to disease progression', 'timeFrame': 'Up to 3 years', 'description': 'Progression-free survival is defined as the time to tumor progression (in-field, distant intrahepatic, extrahepatic) based on mRECIST in months from TheraSphere administration until disease progression or death by any cause using the Kaplan-Meier estimator and 90% confidence intervals will be reported.'}, {'measure': 'Changes in mean Functional Assessment of Cancer Therapy - Hepatobiliary (FACT-Hep) survey results over time', 'timeFrame': 'Up to 6 months', 'description': 'The FACT-Hep is a 45-item self-report instrument developed to assess health-related quality of life (HRQoL) in persons diagnosed with hepatobiliary cancers and consists of the Functional Assessment of Cancer Therapy scale (FACT-G) which is a 27-item questionnaire designed to measure four domains of HRQOL in cancer patients: Physical, social, emotional, and functional well-being and also includes a Hepatobiliary Cancer Subscale (HCS) which consists of an additional 18-items focusing on disease-specific symptoms such as back and stomach pain, gastrointestinal issues, anorexia, weight loss, and jaundice. Each item response score ranges from 0 (not at all) to 4 (very much) with a total score range from 0-180. The higher the score, the better the HRQoL. The change in mean scores over time will be reported.'}, {'measure': 'Changes in mean EuroQol five-dimensional Questionnaire (EQ-5D) survey results over time', 'timeFrame': 'Up to 6 months', 'description': 'EQ-5D is a standardized instrument for measuring generic health status. The health status is measured in terms of five dimensions (5D); mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The respondents self-rate their level of severity for each dimension by selecting one of the following responses: no problems (0), slight problems (1), mild problems (2), moderate problems (3), or severe problems (4) with a particular dimension. Lower scores indicate less issues/problems with that particular health dimension. The change in mean scores over time will be reported.'}, {'measure': 'Best observed tumor response by mRECIST.', 'timeFrame': 'Up to 1 year', 'description': 'Best imaging response at 1 year will be determined based on mRECIST criteria among imaging follow up within 1 year of treatment.'}, {'measure': 'Proportion of participants on an active liver transplant waitlist who receive a transplant', 'timeFrame': 'Up to 3 years', 'description': 'Participants status on the transplant list will be recorded and the proportion of them among all enrolled participants will be reported.'}, {'measure': 'Proportion of participants requiring additional therapies', 'timeFrame': 'Up to 3 years', 'description': 'The proportion of participants that need subsequent loco-regional therapies as deemed clinically indicated after TheraSphere administration will be reported.'}, {'measure': 'Proportion of participants with Complete pathologic response (CPN)', 'timeFrame': 'Up to 3 years', 'description': 'The proportion of participants who underwent a liver transplant and demonstrated CPN post-transplant will be reported.'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': True}, 'conditionsModule': {'conditions': ['Hepatocellular Carcinoma', 'Unresectable Hepatocellular Carcinoma', 'Hepatocellular Cancer', 'Hepatocellular Carcinoma Non-resectable']}, 'descriptionModule': {'briefSummary': 'This is a prospective, single-blinded, single-arm, open-label Phase II trial of trans-arterial radiation segmentectomy using Yttrium-90 glass microspheres (TheraSphere®) for Hepatocellular Carcinoma (HCC) participants with unresectable Barcelona clinic liver cancer (BCLC) stage A disease.', 'detailedDescription': 'PRIMARY OBJECTIVES:\n\nI. To evaluate the objective response rate (ORR) after radiation segmentectomy in participants with BCLC Stage A HCC and 1) a single solitary tumor measuring 2-5 centimeters (cm) and 2) 2 or 3 lesions each ≤ 3 cm.\n\nII. To assess the safety of radiation segmentectomy.\n\nSECONDARY OBJECTIVES:\n\nI. To evaluate transplant-free survival.\n\nII. To evaluate progression-free survival.\n\nIII. To evaluate the quality of life of participants.\n\nIV. To evaluate the best imaging response. V. To determine the proportion of participants who remain active on the wait list for liver transplant and eventually are transplanted.\n\nVI. The evaluate the number of participants that need additional treatment after TheraSphere® administration.\n\nVII. Complete pathologic response (CPN) on liver explants among participants who underwent liver transplant.\n\nParticipants will undergo a single TheraSphere® administration and followed for quality-of-life outcomes and survival for up to 3 years after treatment. Participants will be censored at time of future transplant or if death occurs at any time after treatment.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '22 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n1. Participants must have histologically or imaging-confirmed confirmed HCC.\n2. Group 1: Solitary tumor measuring 2-5 cm Or Group 2: 2-3 tumors each ≤ 3 cm in diameter.\n3. No prior therapy to target tumor(s).\n4. Not a candidate for surgical resection or thermal ablation after multidisciplinary assessment.\n5. Age ≥22 years.\n6. Eastern Cooperative Oncology Group (ECOG) performance status = 0 or 1.\n7. Demonstrated adequate organ function as defined below:\n\n 1. Total bilirubin ≤3.0 mg/dL, unless elevated due to Gilbert's syndrome and direct bilirubin is within normal limits.\n 2. aspartate aminotransferase (AST)/serum glutamic-oxaloacetic transaminase (SGOT) ≤5 X institutional upper limit of normal.\n 3. alanine aminotransferase (ALT)/serum glutamic-pyruvic transaminase (SGPT) ≤5 X institutional upper limit of normal.\n 4. Creatinine Glomerular filtration rate (GFR) \\> 30 ml/min.\n8. Child-Pugh score ≤ B7\n9. Albumin-bilirubin (ALBI) score 1-2\n10. Participants who have received systemic therapy for HCC will be excluded from the trial.\n11. Ability to understand a written informed consent document, and the willingness to sign it.\n12. Human immunodeficiency virus (HIV)-infected participants on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial.\n13. Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.\n\nExclusion Criteria:\n\n1. Macrovascular tumor invasion or infiltrative appearance of hepatocellular carcinoma.\n2. History of severe allergy to iodinated contrast agents despite appropriate premedication.\n3. Is currently receiving any other anti-cancer agents and any previous therapy with a device that uses Y90 as the radioisotope.\n4. Symptomatic heart failure or severe valvular insufficiency.\n5. Symptomatic pulmonary hypertension or lung disease.\n6. Symptomatic ascites.\n7. Severe uncontrolled coagulopathy International Normalized Ratio (INR) ≥ 3.0 or Platelet ≤ 20,000.\n8. Main vein thrombosis (portal vein, both bland and tumor thrombus). Note: Less than lobar portal vein thrombosis is allowable only if the thrombus is bland.\n9. Pregnant women are excluded from this study because TheraSphere emits radiation with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with TheraSphere, breastfeeding should be discontinued if the mother is treated with TheraSphere.\n10. Lung-shunt fraction (LSF) resulting in anticipated lung dose of \\>30 Gray (Gy).\n11. History of sphincterotomy, biliary-enteric anastomosis, or other biliary tract instrumentation. Note: Prior cholecystectomy with or without bile duct exploration is permitted.\n12. Tumor perfused by extrahepatic collateral arteries.\n13. Prior partial hepatectomy.\n14. Psychiatric illness, other significant medical illness, or social situation which, in the investigator's opinion, would limit compliance or ability to comply with study requirements.\n15. History of or current extrahepatic cancer.\n16. Pulmonary insufficiency (defined by an arterial oxygen pressure (Pa,O2) of \\< 60 mmHg, or oxygen saturation (Sa,O2) of \\< 90%)."}, 'identificationModule': {'nctId': 'NCT07110233', 'briefTitle': 'Yttrium-90 Radiation Segmentectomy for Hepatocellular Carcinoma', 'organization': {'class': 'OTHER', 'fullName': 'University of California, San Francisco'}, 'officialTitle': 'Prospective Phase 2 Trial of Yttrium-90 Radiation Segmentectomy for Unresectable Hepatocellular Carcinoma', 'orgStudyIdInfo': {'id': 'RLOKKEN-A'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Group 1. TheraSphere® Yttrium-90 microspheres', 'description': "Participants with a single tumor measuring 2-5 cm will receive one dose of TheraSphere® \\>250 Gy, and ideally \\> 400 Gy at the treating physician's discretion. Participants will be monitored for safety and complete quality of life questionnaires.", 'interventionNames': ['Device: TheraSphere® Yttrium-90 microspheres', 'Other: Health Related Quality of Life Questionnaires (HRQOL)']}, {'type': 'EXPERIMENTAL', 'label': 'Group 2. TheraSphere® Yttrium-90 microspheres', 'description': "Participants with 2-3 tumors ≤ 3 cm in diameter (T2 disease) will receive one dose of TheraSphere® \\>250 Gy, and ideally \\> 400 Gy at the treating physician's discretion. Participants will be monitored for safety and complete quality of life questionnaires.", 'interventionNames': ['Device: TheraSphere® Yttrium-90 microspheres', 'Other: Health Related Quality of Life Questionnaires (HRQOL)']}], 'interventions': [{'name': 'TheraSphere® Yttrium-90 microspheres', 'type': 'DEVICE', 'otherNames': ['TheraSphere®', 'Yttrium-90 microspheres', 'Microspheres Radionuclide'], 'description': 'Administered intra-arterially', 'armGroupLabels': ['Group 1. TheraSphere® Yttrium-90 microspheres', 'Group 2. TheraSphere® Yttrium-90 microspheres']}, {'name': 'Health Related Quality of Life Questionnaires (HRQOL)', 'type': 'OTHER', 'otherNames': ['HRQOL Questionnaires'], 'description': 'Surveys administered', 'armGroupLabels': ['Group 1. TheraSphere® Yttrium-90 microspheres', 'Group 2. TheraSphere® Yttrium-90 microspheres']}]}, 'contactsLocationsModule': {'locations': [{'zip': '94143', 'city': 'San Francisco', 'state': 'California', 'country': 'United States', 'contacts': [{'name': 'Maya Aslam', 'role': 'CONTACT', 'email': 'Maya.Aslam@ucsf.edu', 'phone': '(415) 514-8987'}, {'name': 'Ryan Lokken, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'University of California, San Francisco', 'geoPoint': {'lat': 37.77493, 'lon': -122.41942}}], 'centralContacts': [{'name': 'Maya Aslam', 'role': 'CONTACT', 'email': 'Maya.Aslam@ucsf.edu', 'phone': '(415) 514-8987'}], 'overallOfficials': [{'name': 'Ryan Lokken, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of California, San Francisco'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of California, San Francisco', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'Associate Professor of Clinical Radiology', 'investigatorFullName': 'R. Peter Lokken, MD, MPH', 'investigatorAffiliation': 'University of California, San Francisco'}}}}