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Cutaneous Toxic Effects of BRAF Inhibitors Alone and in Combination With MEK Inhibitors for Metastatic Melanoma
Author(s) -
Giuliana Carlos,
Rachael Anforth,
Arthur Clements,
Alexander M. Menzies,
Matteo S. Carlino,
Shaun Chou,
Pablo FernándezPeñas
Publication year - 2015
Publication title -
jama dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.128
H-Index - 166
eISSN - 2168-6084
pISSN - 2168-6068
DOI - 10.1001/jamadermatol.2015.1745
Subject(s) - medicine , vemurafenib , dabrafenib , trametinib , mek inhibitor , adverse effect , oncology , melanoma , skin cancer , cancer , pharmacology , cancer research , metastatic melanoma , kinase , mapk/erk pathway , biology , microbiology and biotechnology
The cutaneous adverse effects of the BRAF inhibitors vemurafenib and dabrafenib mesylate in the treatment of metastatic melanoma have been well reported. The addition of a MEK inhibitor to a BRAF inhibitor improves the blockade of the mitogen-activated protein kinase pathway. The combination of dabrafenib with the MEK inhibitor trametinib dimethyl sulfoxide (CombiDT therapy) increases response rate and survival compared with a BRAF inhibitor alone. Clinical trials have suggested that CombiDT therapy induces fewer cutaneous toxic effects than a single-agent BRAF inhibitor. To our knowledge, a direct comparison has not been performed before.

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