Y-90 Versus SBRT for Inoperable HCC
NCT05157451 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2023-03-23
Summary
This phase II trial tests whether Y-90 segmentectomy (internal radiation) versus stereotactic body radiation therapy (external radiation) is more optimal in treating inoperable liver cancer. Y-90 segmentectomy consists into very tiny radioactive glass beads that can be injected into the liver through the blood vessels supplying the liver. Stereotactic body radiation therapy uses special equipment to position a patient and deliver external radiation to tumors with high precision. This study many help doctors determine which treatment, Y-90 segmentectomy or SBRT, works better in treating liver cancer.
Conditions
- Hepatocellular Carcinoma
- Stage I Hepatocellular Carcinoma AJCC v8
- Stage IA Hepatocellular Carcinoma AJCC v8
- Stage IB Hepatocellular Carcinoma AJCC v8
- Stage II Hepatocellular Carcinoma AJCC v8
- Stage III Hepatocellular Carcinoma AJCC v8
- Stage IIIA Hepatocellular Carcinoma AJCC v8
- Stage IIIB Hepatocellular Carcinoma AJCC v8
- Stage IVA Hepatocellular Carcinoma AJCC v8
Interventions
- OTHER
-
Quality of Life
Ancillary studies
- OTHER
-
Questionnaire Administration
Ancillary studies
- RADIATION
-
Stereotactic Body Radiation Therapy
Undergo SBRT
- PROCEDURE
-
Yttrium-90 Microsphere Radioembolization
Given via injection
Sponsors & Collaborators
-
American Society of Clinical Oncology
collaborator OTHER -
Medical Research Foundation, Oregon
collaborator OTHER -
Oregon Health and Science University
collaborator OTHER -
Radiation Oncology Institute
collaborator UNKNOWN -
Radiological Society of North America
collaborator OTHER -
OHSU Knight Cancer Institute
lead OTHER
Principal Investigators
-
Nima Nabavizadeh · OHSU Knight Cancer Institute
Study Design
- Allocation
- RANDOMIZED
- Purpose
- DEVICE_FEASIBILITY
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-12-01
- Primary Completion
- 2026-01-05
- Completion
- 2026-01-05
- FDA Device
- Yes
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