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Activity of trametinib in K601E and L597Q BRAF mutation-positive metastatic melanoma

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MELANOMA RESEARCH
卷 24, 期 5, 页码 504-508

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CMR.0000000000000099

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BRAF; K601E; L597; MEK inhibition; melanoma; metastatic; trametinib

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BRAF and MEK inhibitors are not established treatments for non-V600 mutation-positive metastatic melanoma. We carried out a retrospective analysis of efficacy and safety in four patients with BRAF K601E and one patient with L597Q mutation-positive metastatic melanoma treated with the MEK inhibitor trametinib. Three patients achieved a RECIST partial response, including the patient with an L597Q mutation. Paired biopsies available in one of the five patients showed reduced phospho-ERK signalling and this corresponded to a metabolic response on F-18-fluorodeoxyglucose-PET scanning. Trametinib toxicity was manageable. Trametinib has antitumour activity in patients with BRAF K601E and L597Q mutation-positive metastatic melanoma. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.

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