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Treating malignant melanoma when a rare BRAF V600M mutation is present: case report and literature review Cover

Treating malignant melanoma when a rare BRAF V600M mutation is present: case report and literature review

Open Access
|May 2018

Abstract

Recent years have brought major advances in the treatment of malignant melanoma. One such an advance is the treatment with BRAF tyrosine-kinase inhibitors in metastatic malignant melanomas that harbor mutations in the BRAF gene. The trials that have been performed in this setting have demonstrated superior response rates and increased overall survival, however, they mostly included patients with melanomas carrying the more common V600E and V600K mutations, not being able to assess the benefit of these treatments in situations where more rare mutations of the BRAF gene are present. We present the evolution of a patient with malignant melanoma with a rare V600M mutation in the BRAF gene, that was eventually treated with vemurafenib. Also we present a brief review of the major phase III trials that showed benefit with tyrosine-kinase inhibitors in BRAF mutated melanoma, with respect to the BRAF mutations included.

DOI: https://doi.org/10.1515/rjim-2017-0044 | Journal eISSN: 2501-062X | Journal ISSN: 1220-4749
Language: English
Page range: 122 - 126
Submitted on: Oct 15, 2017
Published on: May 17, 2018
Published by: N.G. Lupu Internal Medicine Foundation
In partnership with: Paradigm Publishing Services
Publication frequency: 4 times per year

© 2018 Andrei Popescu, Andrei Haidar, Rodica Maricela Anghel, published by N.G. Lupu Internal Medicine Foundation
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.