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Updated: Feb 18, 2026

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
Published on: June 7, 2019
Treating malignant melanoma when a rare BRAF V600M mutation is present: case report and literature review
Andrei Popescu1,2, Andrei Haidar3, Rodica Maricela Anghel4,2
1Medical Oncology Department, "Colentina" Clinical Hospital, Bucharest, Romania.
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.
Insights
BRAF tyrosine-kinase inhibitors show promise for metastatic melanoma. This study details a patient with a rare BRAF V600M mutation treated successfully with vemurafenib, expanding treatment insights.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- Malignant melanoma treatment has advanced with BRAF tyrosine-kinase inhibitors.
- These inhibitors are effective in metastatic melanomas with BRAF gene mutations.
- Clinical trials primarily focused on common BRAF V600E and V600K mutations.
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