RecruitingPhase 2Phase 3NCT06904170

Durvalumab and Tremelimumab With or Without Hepatic Arterial Infusion of Chemotherapy in Hepatocellular Carcinoma

An Integrated Phase II/III Randomized Study Comparing Durvalumab and Tremelimumab +/- Hepatic ArteriaL Infusion Chemotherapy With GEMOX in Hepatocellular Carcinoma With High Tumor burdEn


Sponsor

UNICANCER

Enrollment

196 participants

Start Date

Nov 14, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Liver cancer is a highly lethal malignancy and has become increasingly important in western countries. The management of liver cancer is complex. In advanced disease, two combinations of immunotherapies are recommanded as first line (atezolizumab-bevacizumab or durvalumab-tremelimumab). Results in patients with high tumor burden (Portal vein thrombosis Vp3 or Vp4, or tumoral liver involvement \>50%) are less impressive. Innovative combinations are necessary to improve the outcome of patients. Recently, control trials conducted in Asia highlighted the benefit of hepatic arterial infusion chemotherapy, especially in patients with high tumor burden. Studies including a limited number of patients shown that the combination seems feasible. ALICE is a randomized multicentric Phase II/Phase III trial conducted in French medical centers, evaluating the efficacy and safety of durvalumab+tremelimumab with or without Hepatic Arterial Infusion Chemotherapy of the GEMOX regimen (gemcitabine + oxaliplatin), in patients with high tumor burden. Oxaliplatin induce immunogenic cell death, and gemcitabin deplete regulatory immune cells. The GEMOX regimen thus has the potential for a synergic effect with immunotherapy in HCC. The trial will provide an innovative treatment to patients with no alternative for locoregional treatment, and with limited results with actual systemic treatments. It will also be the first trial of Hepatic Arterial infusion for such patients in the western population.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding a liver-directed chemotherapy infusion (HAIC) to a combination of two immunotherapy drugs (durvalumab and tremelimumab) improves outcomes in people with advanced liver cancer (hepatocellular carcinoma) that involves major blood vessels or more than half the liver. **You may be eligible if...** - You are 18 or older - You have been diagnosed with liver cancer (HCC) with a high tumor burden — meaning it involves a major portal vein branch, spreads across both sides of the liver, or takes up more than 50% of the liver - Your liver function is preserved (Child-Pugh A) - Your general health is good (ECOG 0–1) - You weigh more than 30 kg and have at least one measurable tumor - You are expected to live at least 12 more weeks **You may NOT be eligible if...** - Your liver function is severely impaired - You have had prior systemic therapy for liver cancer - You have active autoimmune disease or prior immunotherapy treatment - You have uncontrolled infections or other serious conditions 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

DRUGDurvalumab Plus Tremelimumab

Systemic infusion of : Tremelimumab 300 mg, single dose at Cycle 1 Durvalumab 1500 mg at Cycle 1 then every 4 weeks until disease progression or unacceptable toxicity. Durvalumab and Tremelimumab will be delivered during a single angiography. Implantable catheter is also allowed. Durvalumab infusion will start 1 hour after the end of the tremelimumab infusion.

DRUGHAIC (GEMOX)

Hepatic Arterial Infusion of Chemotherapy (HAIC) : Gemcitabine 1000 mg/m² over 30 minutes, followed by Oxaliplatin 100 mg/m² over 2 hours. Administered every 2 weeks for 4 cycles. When a Durvalumab cycle match with an HAIC infusion, HAIC will be delivered on the same day.


Locations(11)

CHU de Bordeaux

Bordeaux, France

AP-HP Hôpital Beaujon

Clichy, France

Centre Georges Francois Leclerc

Dijon, France

Hôpital Saint Joseph

Marseille, France

CHU de Montpellier

Montpellier, France

CHU Hôtel-Dieu

Nantes, France

AP-HP Hôpital Cochin

Paris, France

CHU de Poitiers

Poitiers, France

Centre Eugene Marquis

Rennes, France

CHRU de Strasbourg

Strasbourg, France

CHU de Rangueil

Toulouse, France

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NCT06904170


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