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Anal Mucosal Melanoma with <i>KIT</i>-Activating Mutation and Response to Imatinib Therapy – Case Report and Review of the Literature
Author(s) -
Imke Satzger,
Uta Küttler,
B. Völker,
Florian Schenck,
Alexander Kapp,
Ralf Gutzmer
Publication year - 2009
Publication title -
dermatology
Language(s) - English
Resource type - Journals
eISSN - 1421-9832
pISSN - 1018-8665
DOI - 10.1159/000265558
Subject(s) - imatinib , sunitinib , sorafenib , medicine , mucosal melanoma , dasatinib , melanoma , gist , cancer research , stromal tumor , targeted therapy , oncology , stromal cell , cancer , hepatocellular carcinoma , myeloid leukemia
Previously an increased frequency of KIT aberrations in mucosal melanomas was reported, whereas c-KIT in most types of cutaneous melanomas does not appear to be of pathogenetic importance. Imatinib has become the standard of care in other cancers with KIT mutations such as gastrointestinal stromal tumors. Recently 12 cases of metastatic melanoma and KIT-activating mutations have been published to be successfully treated with c-KIT blockers such as imatinib, sunitinib, dasatinib or sorafenib. We report here on one of our patients with KIT-activating mutation in metastatic anal mucosal melanoma, who showed a response to imatinib therapy and summarize the available literature regarding this new therapeutic option.

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