RecruitingPhase 2NCT06999707

Photon Radiotherapy Plus Tremelimumab/Durvalumab for BCLC Stage B and C HCC

Photon Radiotherapy Combined With Tremelimumab and Durvalumab for BCLC Stage B and C Hepatocellular Carcinoma


Sponsor

Chang Gung Memorial Hospital

Enrollment

45 participants

Start Date

May 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Tremelimumab plus durvalumab (the STRIDE regimen) is an approved first-line therapy for unresectable hepatocellular carcinoma (HCC); however, it demonstrates limited efficacy, with an objective response rate (ORR) of only 20.1%. Radiation therapy (RT) is highly effective in controlling localized solid tumors and has become an integral component of the treatment algorithm for unresectable HCC. Preclinical studies have shown that combining RT with PD-L1/PD-1 blockade promotes immunogenic cell death and enhances antigen presentation by dendritic cells, thereby boosting systemic T cell-mediated antitumor responses in mouse models. The addition of CTLA-4 inhibition further enhances antigen cross-priming following RT. Recent retrospective data also indicate that combining RT with immune-oncology agents is associated with improved overall survival and prolonged time to progression compared to RT or immunotherapy alone. However, the clinical benefit and immunologic impact of combining RT with tremelimumab and durvalumab have not yet been evaluated in prospective clinical trials for unresectable HCC. This phase II, single-arm clinical trial aims to assess the safety, efficacy, and immunologic effects of combining proton RT with tremelimumab and durvalumab in patients with unresectable HCC.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether combining standard photon (X-ray) radiation therapy with two immunotherapy drugs (tremelimumab and durvalumab) can improve outcomes for people with liver cancer (hepatocellular carcinoma, or HCC) that cannot be surgically removed or transplanted. **You may be eligible if...** - You are 18 or older with liver cancer that cannot be surgically removed - Your liver cancer is at an intermediate or advanced stage (BCLC stage B or C) - Your liver function is relatively preserved (Child-Pugh score 5–6) - Your blood counts, liver, and kidney labs are within acceptable ranges - You have been tested for hepatitis B and C **You may NOT be eligible if...** - You have another active cancer - Your liver function is significantly impaired - You have active autoimmune disease or take immunosuppressant drugs - You are pregnant or breastfeeding - Prior treatments disqualify you per study criteria Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONPhoton radiotherapy

* 39.6-72.6 Gy in 22 fractions for tumors ≤1 cm from hepatic hilum, bowel, and heart. * 30-66 Gy in 10 fractions for tumors \>1 cm from hepatic hilum, bowel, and heart. * 27.5-50 Gy in 5 fractions using stereotactic body radiation therapy (SBRT) techniques

DRUGTremelimumab

Tremelimumab 300 mg will be administered as an IV infusion for one dose

DRUGDurvalumab

Treatment Duration Guidelines: \* Complete Response (CR): Patients who achieve a CR within one year of treatment will continue durvalumab for a total duration of two years. \* Partial Response (PR): Patients who achieve a PR should continue durvalumab until achieving CR, disease progression (PD), or for a total duration of two years. \* Stable Disease (SD): Patients with SD will receive duvalumab for a total of 6 doses.


Locations(1)

Chang Gung Memorial Hospital at Linkou

Taoyuan City, Taiwan, Taiwan

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NCT06999707


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