Title :

Nivolumab versus sorafenib in advanced hepatocellular carcinoma (CheckMate 459): a randomised, multicentre, open-label, phase 3 trial.

Author(s) :

Yau, T. [Auteur]
Park, J. W. [Auteur]
Finn, R. S. [Auteur]
Cheng, A. L. [Auteur]
Mathurin, Philippe [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Edeline, Julien [Auteur]
CRLCC Eugène Marquis [CRLCC]
Kudo, M. [Auteur]
Harding, J. J. [Auteur]
Merle, Philippe [Auteur]
Hôpital de la Croix-Rousse [CHU - HCL]
Rosmorduc, Olivier [Auteur]
CHU Pitié-Salpêtrière [AP-HP]
Wyrwicz, L. [Auteur]
Schott, E. [Auteur]
Choo, S. P. [Auteur]
Kelley, R. K. [Auteur]
Sieghart, W. [Auteur]
Assenat, Eric [Auteur]
Hôpital Saint Eloi [CHU Montpellier]
Zaucha, R. [Auteur]
Furuse, J. [Auteur]
Abou-Alfa, G. K. [Auteur]
El-Khoueiry, A. B. [Auteur]
Melero, I. [Auteur]
Begic, D. [Auteur]
Chen, G. [Auteur]
Neely, J. [Auteur]
Wisniewski, T. [Auteur]
Tschaika, M. [Auteur]
Sangro, B. [Auteur]

Journal title :

Lancet Oncol

Abbreviated title :

Lancet Oncol

Publication date :

2021-12-18

ISSN :

1474-5488

HAL domain(s) :

Sciences du Vivant [q-bio]

English abstract : [en]

Background Single-agent nivolumab showed durable responses, manageable safety, and promising survival in patients with advanced hepatocellular carcinoma in the phase 1–2 CheckMate 040 study. We aimed to investigate nivolumab ...
Show more >Background Single-agent nivolumab showed durable responses, manageable safety, and promising survival in patients with advanced hepatocellular carcinoma in the phase 1–2 CheckMate 040 study. We aimed to investigate nivolumab monotherapy compared with sorafenib monotherapy in the first-line setting for patients with advanced hepatocellular carcinoma. Methods In this randomised, open-label, phase 3 trial done at medical centres across 22 countries and territories in Asia, Australasia, Europe, and North America, patients at least 18 years old with histologically confirmed advanced hepatocellular carcinoma not eligible for, or whose disease had progressed after, surgery or locoregional treatment; with no previous systemic therapy for hepatocellular carcinoma, with Child-Pugh class A and Eastern Cooperative Oncology Group performance status score of 0 or 1, and regardless of viral hepatitis status were randomly assigned (1:1) via an interactive voice response system to receive nivolumab (240 mg intravenously every 2 weeks) or sorafenib (400 mg orally twice daily) until disease progression or unacceptable toxicity. The primary endpoint was overall survival assessed in the intention-to-treat population. Safety was assessed in all patients who received at least one dose of study drug. This completed trial is registered with ClinicalTrials.gov, NCT02576509. Findings Between Jan 11, 2016, and May 24, 2017, 743 patients were randomly assigned to treatment (nivolumab, n=371; sorafenib, n=372). At the primary analysis, the median follow-up for overall survival was 15·2 months (IQR 5·7–28·0) for the nivolumab group and 13·4 months (5·7–25·9) in the sorafenib group. Median overall survival was 16·4 months (95% CI 13·9–18·4) with nivolumab and 14·7 months (11·9–17·2) with sorafenib (hazard ratio 0·85 [95% CI 0·72–1·02]; p=0·075; minimum follow-up 22·8 months); the protocol-defined significance level of p=0·0419 was not reached. The most common grade 3 or worse treatment-related adverse events were palmar-plantar erythrodysaesthesia (1 [<1%] of 367 patients in the nivolumab group vs 52 [14%] of patients in the sorafenib group), aspartate aminotransferase increase (22 [6%] vs 13 [4%]), and hypertension (0 vs 26 [7%]). Serious treatment-related adverse events were reported in 43 (12%) patients receiving nivolumab and 39 (11%) patients receiving sorafenib. Four deaths in the nivolumab group and one death in the sorafenib group were assessed as treatment related. Interpretation First-line nivolumab treatment did not significantly improve overall survival compared with sorafenib, but clinical activity and a favourable safety profile were observed in patients with advanced hepatocellular carcinoma. Thus, nivolumab might be considered a therapeutic option for patients in whom tyrosine kinase inhibitors and antiangiogenic drugs are contraindicated or have substantial risks.Show less >

Language :

Anglais

Audience :

Internationale

Popular science :

Non

Administrative institution(s) :

Université de Lille
Inserm
CHU Lille

Collections :

• Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286

Submission date :

2024-01-12T05:27:33Z
2024-03-01T08:45:32Z