| Literature DB >> 25473943 |
Mark M Awad1, Ryan J Sullivan.
Abstract
Oncogenic BRAF mutations are present in approximately 40-50% of patients with metastatic melanoma. Targeting BRAF mutations with either small molecule inhibitors of BRAF or one of the downstream mediators of oncogenic BRAF - MEK - is associated with improved outcomes compared with chemotherapy and has led to the US FDA approval of two BRAF inhibitors - vemurafenib and dabrafenib - and the MEK inhibitor trametinib. Further, the combination of dabrafenib and trametinib is well tolerated and associated with higher responses and improved survival compared with single-agent BRAF inhibitors.Entities:
Keywords: BRAF; MEK; melanoma; resistance; targeted therapy
Mesh:
Substances:
Year: 2014 PMID: 25473943 DOI: 10.1586/17512433.2015.974556
Source DB: PubMed Journal: Expert Rev Clin Pharmacol ISSN: 1751-2433 Impact factor: 5.045