Nivolumab and Ipilimumab Combination Treatment in Patients with Advanced Intrahepatic Cholangiocarcinoma and Gallbladder Cancer: Results from the Phase II MoST-CIRCUIT Trial

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Authors: Adnan M. Nagrial, Matteo Salvatore Carlino, Ashray Gunjur, Michael P. Brown, Sam Harris, Craig R. Underhill, Robert Zielinski, Damien Kee, Wei‐Sen Lam, Howard Chan, Rosemary Anne Harrup, Jane Y. So
+14 more Ian M Collins, Michael Michael, Fiona J.M. Chionh, Charles John T. Uy, John Mariadason, Javier Torres, Mandy L. Ballinger, John P. Grady, Elnaz Tavancheh, Jodie Palmer, David Morgan Thomas, Kylie Wilkie, Jonathan Simon Cebon, Oliver Klein
Cited by: 1
References: 39

Abstract

PURPOSE: Anti-PD-1/PD-L1 blockade combined with chemotherapy has become the first-line treatment for advanced biliary tract cancers. Combined anti-PD-1/CTLA-4 blockade using nivolumab and ipilimumab has shown encouraging activity in patients with intrahepatic cholangiocarcinoma (iCCA) and gallbladder carcinoma (GBC) in two trials (CA209-538 and SWOG1609). MoST-CIRCUIT further evaluated combined checkpoint blockade using nivolumab/ipilimumab in patients with advanced iCCA and GBC. PATIENTS AND METHODS: Patients with a maximum of 1 line of prior systemic therapy were enrolled as cohort B into MoST-CIRCUIT, a single-arm, nonrandomized phase 2 trial. Patients received nivolumab 3 mg/kg and ipilimumab 1 mg/kg every 3 weeks for four doses, followed by nivolumab 480 mg every 4 weeks for 96 weeks. Response (RECIST 1.1) was assessed every 12 weeks. Coprimary endpoints were objective response rate (ORR) and 6-month progression-free survival (6-PFS), with the secondary endpoints being median overall survival (mOS), PFS, and treatment-related toxicity. RESULTS: Sixty patients (37 iCCA and 23 GBC) were enrolled; 85% were pretreated, including 13 patients with durvalumab. The ORR was 12% (2% complete response, 10% partial response): 3% and 26% in the iCCA and GBC subgroups, respectively. The 6-PFS was 27% (iCCA 19%; GBC 39%), and mOS was 7 months. In the immunotherapy-naïve population, the ORR was 19% (iCCA 10%; GBC 38%). Severe immune-related adverse events were observed in 20% of patients. CONCLUSIONS: Efficacy was limited in what is the largest biliary tract cancer cohort treated to date with combined anti-CTLA-4/PD-1 blockade. Encouraging activity was observed in the GBC subgroup. Further evaluation of checkpoint inhibition in biliary tract cancer should focus on patients with GBC.

Fields of Study & Subjects

Cholangiocarcinoma and Gallbladder Cancer Studies Cancer Immunotherapy and Biomarkers Liver Diseases and Immunity

Publication details

Journal / source
Clinical Cancer Research
Publisher
American Association for Cancer Research (AACR)
Volume
32
Issue
15
Pages
3203–3212
Publication date
24 April 2026
Language
EN