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-突变型晚期或转移性黑色素瘤的治疗:基本原理、当前试验及迄今证据

Treatment of -mutated advanced or metastatic melanoma: rationale, current trials and evidence to date.

作者信息

Boespflug Amélie, Caramel Julie, Dalle Stephane, Thomas Luc

机构信息

Hospices Civils de Lyon, Dermatology Unit, Lyon, France.

Cancer Research Center of Lyon, Claude Bernard Lyon-1 University, INSERM1052, CNRS 5286, Lyon, France.

出版信息

Ther Adv Med Oncol. 2017 Jul;9(7):481-492. doi: 10.1177/1758834017708160. Epub 2017 May 29.

Abstract

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.

摘要

(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。

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