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Dabrafenib for treatment of BRAF-mutant melanoma

Authors Kainthla R, Kim K, Falchook G

Received 15 August 2013

Accepted for publication 9 October 2013

Published 31 December 2013 Volume 2014:7 Pages 21—29

DOI https://doi.org/10.2147/PGPM.S37220

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3


Radhika Kainthla,1 Kevin B Kim,2 Gerald S Falchook3

1Department of Internal Medicine, Baylor College of Medicine, 2Department of Melanoma Medical Oncology, 3Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA

Abstract: Melanoma has the highest mortality of all the skin cancer subtypes. Historically, chemotherapy and immunologic therapies have yielded only modest results in the treatment of metastatic melanoma. The discovery of prevalent V600 BRAF mutations driving proliferation makes this oncogenic protein an ideal target for therapy. Dabrafenib, a reversible inhibitor of mutant BRAF kinase, improved response rates and median progression-free survival in patients with V600E BRAF-mutant metastatic melanoma, including those with brain metastases. With a well-tolerated toxicity profile, dabrafenib is effective as a monotherapy; however, resistance eventually develops in almost all patients. As a result, current research is exploring the role of combination therapies with dabrafenib to overcome resistance.

Keywords: dabrafenib, metastatic melanoma, V600E BRAF mutation

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