Abstract
Approximately 7 % of melanomas have a BRAF mutation beyond codon 600. These mutations can be BRAF activating without being addressable by an approved BRAF inhibitor. The case of a patient with fulminant metastatic melanoma and a BRAF(L597Q) mutation is presented. It is demonstrated that the tumor shows an excellent response to the MEK inhibitor trametinib. This is an example for possible targeted therapy in a non-V600-mutated melanoma resulting in a 17-month overall survival.
Keywords:
BRAF inhibitor; MEK inhibitor; Survival; Toxicity; Tumor.
MeSH terms
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Antineoplastic Agents / therapeutic use
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Humans
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Male
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Melanoma / drug therapy*
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Melanoma / genetics
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Melanoma / secondary*
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Middle Aged
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Mutation / genetics
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Proto-Oncogene Proteins B-raf / antagonists & inhibitors
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Proto-Oncogene Proteins B-raf / genetics*
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Pyridones / therapeutic use*
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Pyrimidinones / therapeutic use*
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Skin Neoplasms / drug therapy*
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Skin Neoplasms / genetics
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Skin Neoplasms / secondary*
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Treatment Outcome
Substances
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Antineoplastic Agents
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Pyridones
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Pyrimidinones
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trametinib
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BRAF protein, human
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Proto-Oncogene Proteins B-raf