Combined vemurafenib and cobimetinib in BRAF-mutated melanoma - PubMed
- ️Wed Jan 01 2014
Clinical Trial
. 2014 Nov 13;371(20):1867-76.
doi: 10.1056/NEJMoa1408868. Epub 2014 Sep 29.
Paolo A Ascierto, Brigitte Dréno, Victoria Atkinson, Gabriella Liszkay, Michele Maio, Mario Mandalà, Lev Demidov, Daniil Stroyakovskiy, Luc Thomas, Luis de la Cruz-Merino, Caroline Dutriaux, Claus Garbe, Mika A Sovak, Ilsung Chang, Nicholas Choong, Stephen P Hack, Grant A McArthur, Antoni Ribas
Affiliations
- PMID: 25265494
- DOI: 10.1056/NEJMoa1408868
Free article
Clinical Trial
Combined vemurafenib and cobimetinib in BRAF-mutated melanoma
James Larkin et al. N Engl J Med. 2014.
Free article
Abstract
Background: The combined inhibition of BRAF and MEK is hypothesized to improve clinical outcomes in patients with melanoma by preventing or delaying the onset of resistance observed with BRAF inhibitors alone. This randomized phase 3 study evaluated the combination of the BRAF inhibitor vemurafenib and the MEK inhibitor cobimetinib.
Methods: We randomly assigned 495 patients with previously untreated unresectable locally advanced or metastatic BRAF V600 mutation-positive melanoma to receive vemurafenib and cobimetinib (combination group) or vemurafenib and placebo (control group). The primary end point was investigator-assessed progression-free survival.
Results: The median progression-free survival was 9.9 months in the combination group and 6.2 months in the control group (hazard ratio for death or disease progression, 0.51; 95% confidence interval [CI], 0.39 to 0.68; P<0.001). The rate of complete or partial response in the combination group was 68%, as compared with 45% in the control group (P<0.001), including rates of complete response of 10% in the combination group and 4% in the control group. Progression-free survival as assessed by independent review was similar to investigator-assessed progression-free survival. Interim analyses of overall survival showed 9-month survival rates of 81% (95% CI, 75 to 87) in the combination group and 73% (95% CI, 65 to 80) in the control group. Vemurafenib and cobimetinib was associated with a nonsignificantly higher incidence of adverse events of grade 3 or higher, as compared with vemurafenib and placebo (65% vs. 59%), and there was no significant difference in the rate of study-drug discontinuation. The number of secondary cutaneous cancers decreased with the combination therapy.
Conclusions: The addition of cobimetinib to vemurafenib was associated with a significant improvement in progression-free survival among patients with BRAF V600-mutated metastatic melanoma, at the cost of some increase in toxicity. (Funded by F. Hoffmann-La Roche/Genentech; coBRIM ClinicalTrials.gov number, NCT01689519.).
Comment in
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Skin cancer: BRAF and MEK inhibitors-good news comes in twos!
Killock D. Killock D. Nat Rev Clin Oncol. 2014 Dec;11(12):683. doi: 10.1038/nrclinonc.2014.183. Epub 2014 Oct 21. Nat Rev Clin Oncol. 2014. PMID: 25331181 No abstract available.
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Rapid evolution of combination therapy in melanoma.
Curti BD. Curti BD. N Engl J Med. 2014 Nov 13;371(20):1929-30. doi: 10.1056/NEJMe1411158. N Engl J Med. 2014. PMID: 25390744 No abstract available.
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