Safety and Efficacy Study of Radioembolization in Combination With Durvalumab in Locally Advanced and Unresectable HCC
- Conditions
- Hepatocellular Carcinoma
- Interventions
- Radiation: Radioembolization
- Registration Number
- NCT04124991
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Safety and Efficacy Study of Radioembolization with Yttrium-90 Microspheres in Combination with Durvalumab in Locally Advanced Hepatocellular Carcinoma
- Detailed Description
This is a single arm, open-label study to evaluate safety and efficacy of Radioembolization with Yttrium-90 Microspheres in Combination with Durvalumab in Locally Advanced and Unresectable Hepatocellular Carcinoma which to be implemented at a single site in Korea.
Transarterial radioembolization (TARE) with yttrium-90 microspheres will be employed in combination with an intravenous (IV) durvalumab until PD. TARE will be performed before the first dose of durvalumab. Exploratory biomarker testing will be done on tumor tissues prior to treatment and plasma samples prior to treatment and at the time of PD.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 24
- Diagnosed with unequivocal HCC confirmed histologically or diagnosed radiologically
- Locally advanced HCC
- Must have at least 1 untreated measurable disease
- Child-Pugh score ≤7 points
- Adequate normal organ and marrow function.
- Eligible for potentially curative treatment (surgical resection, radio-frequency ablation or immediate liver transplantation)
- Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti- Cytotoxic T-lymphocyte-associated antigen-4 (anti-CTLA-4) antibody
- Any other concurrent malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, papillary thyroid cancer, early gastric cancer, or other cancer for which the patient has been disease-free for at least five years.
- Evidence of extrahepatic metastasi(e)s, except for regional lymph node(s) involvement
- History of leptomeningeal carcinomatosis , History of active primary immunodeficiency
- Current or prior use of immunosuppressive medication within 14 days before the first dose of durvalumab.
Exclusion Criteria Specific to Radioembolization:
•The screening angiogram and technetium-99m macroaggregated albumin (99mTc-MAA) scan are used to determine lobar liver volume from CT or MR images, to identify vascular shunting to the GI tract requiring use of angiographic occlusion techniques and to determine the lung shunt fraction.
Patients who are ineligible to radioembolization meeting the following criteria will not be included in the study. Additional patients will be screened to replace those patients.
- Deposition of yttrium-90 microspheres to the GI tract that cannot be corrected by placement of the catheter distal to collateral vessels or the application of standard angiographic techniques, such as coil embolization to prevent deposition of yttrium-90 microspheres in the GI tract.
- Exposure of radiation to the lungs exceeds 30 Gray (Gy) for a single infusion or 50 Gy cumulative for all infusions of yttrium-90 microspheres.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Yttrium-90 Microspheres in Combination with Durvalumab Radioembolization Transarterial radioembolization (TARE) with yttrium-90 microspheres will be employed in combination with an intravenous (IV) dose of 1500 mg durvalumab every 4 weeks (Q4W) until PD. TARE will be performed 1-2 weeks (7 to 14 days) before the first dose of durvalumab and a maximum of 2 more times during the treatment period, per Investigator discretion. If additional TARE is performed, the interval between additional TARE treatments and administration of durvalumab should be at least 1 week. Yttrium-90 Microspheres in Combination with Durvalumab Durvalumab Transarterial radioembolization (TARE) with yttrium-90 microspheres will be employed in combination with an intravenous (IV) dose of 1500 mg durvalumab every 4 weeks (Q4W) until PD. TARE will be performed 1-2 weeks (7 to 14 days) before the first dose of durvalumab and a maximum of 2 more times during the treatment period, per Investigator discretion. If additional TARE is performed, the interval between additional TARE treatments and administration of durvalumab should be at least 1 week.
- Primary Outcome Measures
Name Time Method TTP From date of enrollment until the date of first documented progression, assessed up to 12 months to evaluate time to progression (TTP) from enrolment using Modified Response Evaluation Criteria in Solid Tumors (mRECIST).
- Secondary Outcome Measures
Name Time Method ORR From date of enrollment until the date of first documented progression, assessed every 8 weeks up to 12 months. Objective Response Rate (ORR) of Target Lesion(s) and Non-Target Lesion(s)
OS From date of enrollment until the date of first documented progression, assessed up to 12 months Overall Survival (OS) from first dose of study drug until the time of data cut-off, as determined by the Investigator.
Number of participants with treatment-related adverse events Until 30 days after radioembolization with yttrium-90 microspheres or the last dose of durvalumab Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Trial Locations
- Locations (1)
Seoul National University Hospital
🇰🇷Seoul, Korea, Republic of