Romanian Journal of Internal Medicine (Jun 2018)

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

  • Popescu Andrei,
  • Haidar Andrei,
  • Anghel Rodica Maricela

DOI
https://doi.org/10.1515/rjim-2017-0044
Journal volume & issue
Vol. 56, no. 2
pp. 122 – 126

Abstract

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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.

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