Targeted Therapy for Melanomas Without BRAF V600 Mutations

被引:0
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作者
Christian Menzer
Jessica C. Hassel
机构
[1] University Hospital Heidelberg,Section of DermatoOncology, Department of Dermatology and National Center for Tumor Diseases (NCT)
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关键词
Melanoma; MAPK pathway; BRAF; MEK; Targeted therapy; BRAF mutation; V600; Non-V600; Trametinib; Binimetinib; Cobimetinib; C-kit; NRAS; Imatinib;
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摘要
Modern therapy of advanced melanoma offers effective targeted therapeutic options in the form of BRAF plus MEK inhibition for patients with BRAF V600 mutations. For patients lacking these mutations, checkpoint inhibition remains the only first-line choice for treatment of metastatic disease. However, approximately half of patients do not respond to immunotherapy, requiring effective options for a second-line treatment. Advances in genetic profiling have found other possible target molecules, especially a wide array of rare non-V600 BRAF mutations which may respond to available targeted therapy.
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页码:831 / 842
页数:11
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