Boespflug Amélie, Caramel Julie, Dalle Stephane, Thomas Luc
Hospices Civils de Lyon, Dermatology Unit, Lyon, France.
Cancer Research Center of Lyon, Claude Bernard Lyon-1 University, INSERM1052, CNRS 5286, Lyon, France.
Ther Adv Med Oncol. 2017 Jul;9(7):481-492. doi: 10.1177/1758834017708160. Epub 2017 May 29.
The disease course of (v-raf murine sarcoma viral oncogene homolog B1)-mutant melanoma has been drastically improved by the arrival of targeted therapies. (neuroblastoma viral oncogene homolog)-mutated melanoma represents 15-25% of all metastatic melanoma patients. It currently does not have an approved targeted therapy. Metastatic patients receive immune-based therapies as first-line treatments, then cytotoxic chemotherapy like carboplatin/paclitaxel (C/P), dacarbazine (DTIC) or temozolomide (TMZ) as a second-line treatment. We will review current preclinical and clinical developments in -mutated melanoma, and analyze ongoing clinical trials that are evaluating the benefit of different targeted and immune-based therapies, either tested as single agents or in combination, in -mutant melanoma.
(v-raf鼠肉瘤病毒癌基因同源物B1)突变型黑色素瘤的病程因靶向治疗的出现而得到显著改善。(神经母细胞瘤病毒癌基因同源物)突变型黑色素瘤占所有转移性黑色素瘤患者的15%-25%。目前它尚无获批的靶向治疗方法。转移性患者接受基于免疫的疗法作为一线治疗,然后接受细胞毒性化疗,如卡铂/紫杉醇(C/P)、达卡巴嗪(DTIC)或替莫唑胺(TMZ)作为二线治疗。我们将回顾目前在 突变型黑色素瘤方面的临床前和临床进展,并分析正在进行的临床试验,这些试验正在评估不同的靶向和基于免疫的疗法(单独或联合使用)在 突变型黑色素瘤中的疗效。