Nivolumab Plus Cabozantinib With or Without Ipilimumab for Advanced Hepatocellular Carcinoma: Results From Cohort 6 of the CheckMate 040 Trial.

Anthony B El-Khoueiry, Jaclyn Neely, Petra Koopmans, Christian Scheffold, Marina Tschaika, Gina M Vaccaro, Giovanni Luca Frassineti, Jordi Bruix, Tarek E Eldawy, Bruno Sangro, Fabio Piscaglia, Antonio Cubillo Gracian, Aiwu Ruth He, Ana Matilla, Su Pin Choo, Mirelis Acosta-Rivera, Armando Santoro, Vittorina Zagonel, Thomas Yau

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2023;41(9):1747-1757

PMID: 36512738

Abstract

PURPOSE

To investigate the safety and efficacy of nivolumab plus cabozantinib with or without ipilimumab in patients with advanced hepatocellular carcinoma.

METHODS

In cohort 6 of the multicohort, open-label, phase I/II CheckMate 040 study, patients who were treatment-naive, sorafenib-intolerant, or had progressed on sorafenib were randomly assigned 1:1 to nivolumab 240 mg once every 2 weeks plus cabozantinib 40 mg once daily (doublet arm); or nivolumab 3 mg/kg every 2 weeks plus cabozantinib 40 mg once daily with ipilimumab 1 mg/kg once every 6 weeks (triplet arm). Primary objectives were safety and tolerability, objective response rate, and duration of response by investigator assessment per RECIST v1.1. Secondary objectives included progression-free survival (by blinded independent central review) and overall survival.

RESULTS

Seventy-one patients were randomly assigned: 36 to the doublet arm and 35 to the triplet arm. After 32.0-month median follow-up, objective response rate (95% CI) was 17% (6 to 33) and 29% (15 to 46) in the doublet and triplet arms, respectively. Median (95% CI) duration of response was 8.3 (6.9 to not estimable) months in the doublet arm and not reached (0.0 to not estimable) in the triplet arm. Median progression-free survival was 5.1 and 4.3 months, and median overall survival was 20.2 and 22.1 months for the doublet and triplet arms, respectively. Grade 3-4 treatment-related adverse events occurred in 50% and 74% of patients and treatment-related adverse events leading to discontinuation were reported for 11% and 23% in the doublet and triplet arms, respectively. There were no treatment-related deaths in either arm.

CONCLUSION

Nivolumab plus cabozantinib with or without ipilimumab showed encouraging preliminary antitumor activity and had consistent safety profiles with those established for the individual drugs in patients with advanced hepatocellular carcinoma.

Address: The University of Hong Kong, Hong Kong, China.; Oncology Unit 1, Veneto Institute of Oncology, IOV-IRCCS, Padova, Italy.; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.; IRCCS Humanitas Research Hospital-Humanitas Cancer Center, Rozzano, Italy.; Fundacion de Investigación, San Juan, Puerto Rico.; National Cancer Center and Curie Oncology, Singapore.; Servicio de Digestivo, Hospital General Universitario Gregorio Marañón, Madrid, Spain.; CIBEREHD, Madrid, Spain.; Georgetown University Hospital, Washington, DC.; Hospital HM Universitario Sanchinarro, Centro Integral Oncológico Clara Campal (HM-CIOCC), Madrid, Spain.; Departamento de Ciencias Médicas Clínicas, Universidad Camilo José Cela, Madrid, Spain.; USC Norris Comprehensive Cancer Center, Los Angeles, CA.; Clinica Universidad de Navarra and CIBEREHD, Pamplona, Spain.; Sacred Heart Health Systems, Pensacola, FL.; BCLC Group, Liver Unit, Hospital Clínic-IDIBAPS, University of Barcelona, CIBEREHD, Barcelona, Spain.; IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori," Meldola, Italy.; Providence Cancer Institute, Portland, OR.; Bristol Myers Squibb, Princeton, NJ.; Exelixis, Inc, Alameda, CA.; Division of Internal Medicine, Hepatobiliary and Immunoallergic Diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
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