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Combined Nivolumab and Ipilimumab or Monotherapy in Untreated Melanoma.

James Larkin ,
Vanna Chiarion-Sileni ,
Rene Gonzalez ,
Jean Jacques Grob ,
C Lance Cowey ,
Christopher D Lao ,
Dirk Schadendorf ,
Reinhard Dummer ,
Michael Smylie ,
Piotr Rutkowski ,
Pier F Ferrucci ,
Andrew Hill ,
John Wagstaff ,
Matteo S Carlino ,
John B Haanen ,
Michele Maio ,
Ivan Marquez-Rodas ,
Grant A McArthur ,
Paolo A Ascierto ,
Georgina V Long ,
Margaret K Callahan ,
Michael A Postow ,
Kenneth Grossmann ,
Mario Sznol ,
Brigitte Dreno ,
Lars Bastholt ,
Arvin Yang ,
Linda M Rollin ,
Christine Horak ,
F Stephen Hodi ,
Jedd D Wolchok

Abstract

METHODS

We assigned, in a 1:1:1 ratio, 945 previously untreated patients with unresectable stage III or IV melanoma to nivolumab alone, nivolumab plus ipilimumab, or ipilimumab alone. Progression-free survival and overall survival were coprimary end points. Results regarding progression-free survival are presented here.

CONCLUSIONS

Among previously untreated patients with metastatic melanoma, nivolumab alone or combined with ipilimumab resulted in significantly longer progression-free survival than ipilimumab alone. In patients with PD-L1-negative tumors, the combination of PD-1 and CTLA-4 blockade was more effective than either agent alone. (Funded by Bristol-Myers Squibb; CheckMate 067 ClinicalTrials.gov number, NCT01844505.).

RESULTS

The median progression-free survival was 11.5 months (95% confidence interval [CI], 8.9 to 16.7) with nivolumab plus ipilimumab, as compared with 2.9 months (95% CI, 2.8 to 3.4) with ipilimumab (hazard ratio for death or disease progression, 0.42; 99.5% CI, 0.31 to 0.57; P<0.001), and 6.9 months (95% CI, 4.3 to 9.5) with nivolumab (hazard ratio for the comparison with ipilimumab, 0.57; 99.5% CI, 0.43 to 0.76; P<0.001). In patients with tumors positive for the PD-1 ligand (PD-L1), the median progression-free survival was 14.0 months in the nivolumab-plus-ipilimumab group and in the nivolumab group, but in patients with PD-L1-negative tumors, progression-free survival was longer with the combination therapy than with nivolumab alone (11.2 months [95% CI, 8.0 to not reached] vs. 5.3 months [95% CI, 2.8 to 7.1]). Treatment-related adverse events of grade 3 or 4 occurred in 16.3% of the patients in the nivolumab group, 55.0% of those in the nivolumab-plus-ipilimumab group, and 27.3% of those in the ipilimumab group.

BACKGROUND

Nivolumab (a programmed death 1 [PD-1] checkpoint inhibitor) and ipilimumab (a cytotoxic T-lymphocyte-associated antigen 4 [CTLA-4] checkpoint inhibitor) have been shown to have complementary activity in metastatic melanoma. In this randomized, double-blind, phase 3 study, nivolumab alone or nivolumab plus ipilimumab was compared with ipilimumab alone in patients with metastatic melanoma.

More about this publication

The New England journal of medicine

Volume 373
Issue nr. 1
Pages 23-34
Publication date 02-07-2015

Full text links

Publisher website (DOI) 10.1056/NEJMoa1504030
Europe PubMed Central 26027431
Pubmed 26027431

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