Incidence, course, and management of toxicities associated with cobimetinib in combination with vemurafenib in the coBRIM study.
Identifieur interne : 000999 ( Main/Exploration ); précédent : 000998; suivant : 000A00Incidence, course, and management of toxicities associated with cobimetinib in combination with vemurafenib in the coBRIM study.
Auteurs : B. Dréno [France] ; A. Ribas [États-Unis] ; J. Larkin [Royaume-Uni] ; P A Ascierto [Italie] ; A. Hauschild [Allemagne] ; L. Thomas [France] ; J-J Grob [France] ; D O Koralek [États-Unis] ; I. Rooney [États-Unis] ; J J Hsu [États-Unis] ; E F Mckenna [États-Unis] ; G A Mcarthur [Australie]Source :
- Annals of oncology : official journal of the European Society for Medical Oncology [ 1569-8041 ] ; 2017.
Abstract
In the coBRIM phase III trial, the addition of cobimetinib, an MEK inhibitor, to vemurafenib, a BRAF inhibitor, significantly improved progression-free survival [hazard ratio (HR), 0.58; P < 0.0001] and overall survival (HR, 0.70; P = 0.005) in advanced BRAF-mutated melanoma. Here, we report on the incidence, course, and management of key adverse events (AEs) in the coBRIM study.
DOI: 10.1093/annonc/mdx040
PubMed: 28444112
Affiliations:
- Allemagne, Australie, France, Italie, Royaume-Uni, États-Unis
- Angleterre, Californie, Grand Londres, Pays de la Loire, Provence-Alpes-Côte d'Azur, Schleswig-Holstein, Victoria (État)
- Kiel, Londres, Los Angeles, Marseille, Melbourne, Nantes
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Le document en format XML
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<front><div type="abstract" xml:lang="en">In the coBRIM phase III trial, the addition of cobimetinib, an MEK inhibitor, to vemurafenib, a BRAF inhibitor, significantly improved progression-free survival [hazard ratio (HR), 0.58; P < 0.0001] and overall survival (HR, 0.70; P = 0.005) in advanced BRAF-mutated melanoma. Here, we report on the incidence, course, and management of key adverse events (AEs) in the coBRIM study.</div>
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