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OncoMatch/Clinical Trials/NCT06904170

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

Is NCT06904170 recruiting? Yes, currently enrolling (May 2026). This Phase 2/3 trial studies multiple treatments including Durvalumab Plus Tremelimumab and HAIC (GEMOX) for hepatocellular carcinoma.

Phase 2/3RecruitingUNICANCERNCT06904170Data as of May 2026

Treatment: Durvalumab Plus Tremelimumab · HAIC (GEMOX)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.

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Extracted eligibility criteria

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic treatment

Previous systemic treatment (either immunotherapy, anti-angiogenics, chemotherapy, or any combination thereof)

Cannot have received: hepatic arterial infusion of chemotherapy

Previous treatment with hepatic arterial infusion of chemotherapy

Lab requirements

Blood counts

Haemoglobin ≥ 7.5 g/dL (exclude if 7.5 < Hgb < 9.0 and active/chronic bleeding); Platelet count ≥75 × 10^9/L; Absolute neutrophil count (ANC) ≥1.0 × 10^9 /L

Kidney function

creatinine clearance > 40 mL/min (according to Cockcroft or MDRD formula)

Liver function

Child-Pugh A liver function; AST (SGOT)/ALT (SGPT) ≤5x ULN; Serum bilirubin ≤1.5 x institutional upper limit of normal (ULN); INR < 2.3

Cardiac function

Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) < 470 ms calculated from 3 ECGs

Child-Pugh A liver function; Haemoglobin ≥ 7.5 g/dL; Platelet count ≥75 × 10^9/L; ANC ≥1.0 × 10^9 /L; creatinine clearance > 40 mL/min; AST/ALT ≤5x ULN; Serum bilirubin ≤1.5 x ULN; INR < 2.3; QTcF < 470 ms

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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