Journal article
Imatinib for Melanomas Harboring Mutationally Activated or Amplified KIT Arising on Mucosal, Acral, and Chronically Sun-Damaged Skin
Abstract
PURPOSE: Amplifications and mutations in the KIT proto-oncogene in subsets of melanomas provide therapeutic opportunities.
PATIENTS AND METHODS: We conducted a multicenter phase II trial of imatinib in metastatic mucosal, acral, or chronically sun-damaged (CSD) melanoma with KIT amplifications and/or mutations. Patients received imatinib 400 mg once per day or 400 mg twice per day if there was no initial response. Dose reductions were permitted …
Authors
Hodi FS; Corless CL; Giobbie-Hurder A; Fletcher JA; Zhu M; Marino-Enriquez A; Friedlander P; Gonzalez R; Weber JS; Gajewski TF
Journal
Journal of Clinical Oncology, Vol. 31, No. 26, pp. 3182–3190
Publisher
American Society of Clinical Oncology (ASCO)
Publication Date
September 10, 2013
DOI
10.1200/jco.2012.47.7836
ISSN
0732-183X
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AdultAgedAged, 80 and overAntineoplastic AgentsBenzamidesBiomarkers, TumorChronic DiseaseFemaleGTP PhosphohydrolasesGene AmplificationHumansImatinib MesylateMaleMelanomaMembrane ProteinsMiddle AgedMucous MembraneMutationNeoplasm Recurrence, LocalPiperazinesPrognosisProto-Oncogene MasProto-Oncogene Proteins c-kitPyrimidinesSkin NeoplasmsSunlightSurvival Rate