BRAF和MEK抑制剂在黑色素瘤患者免疫治疗时代的应用。

IF 1.3
Contemporary oncology (Poznan, Poland) Pub Date : 2018-03-01 Epub Date: 2018-03-05 DOI:10.5114/wo.2018.73890
Jacek Mackiewicz, Andrzej Mackiewicz
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引用次数: 57

摘要

随着新药的批准,晚期黑色素瘤的治疗前景正在发生巨大变化。Vemurafenib是首个被批准用于治疗braf突变晚期黑色素瘤的靶向药物。然而,使用BRAF抑制剂治疗与获得性耐药有关,大约6个月后,一半的患者会出现获得性耐药。MEK和BRAF抑制剂联合治疗可延长耐药时间,从而延长治疗患者的总生存期。在相同的患者群体中,使用针对免疫检查点抑制剂的抗体治疗也观察到类似的临床益处。由于比较这两种治疗策略的随机研究结果尚未公布,因此braf突变黑色素瘤患者的最佳一线和二线治疗方案尚不清楚。目前,3期研究也在评估靶向治疗联合免疫治疗在BRAF突变型和BRAF野生型晚期黑色素瘤患者中的疗效。确定一种生物标志物,用于选择从治疗中获益最多的患者,对于进一步改善晚期黑色素瘤患者的生存至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BRAF and MEK inhibitors in the era of immunotherapy in melanoma patients.

The treatment landscape in advanced melanoma is changing dramatically with the approval of new drugs. Vemurafenib was the first approved targeted agent for the treatment of BRAF-mutant advanced melanoma. However, treatment with a BRAF inhibitor is linked with acquired resistance occurring in half of the patients after approximately six months. Combination of MEK and BRAF inhibitor therapy results in extension of the time to resistance, translating into longer overall survival of treated patients. Similar clinical benefits are observed with therapy using antibodies against immune-checkpoint inhibitors in the same patient population. Due to the fact that results of randomised studies comparing these two treatment strategies back to back have not been presented yet, the best first and second line treatment option in patients with BRAF-mutant melanoma is unknown. Currently, phase 3 studies are also evaluating the efficacy of targeted therapy combined with immunotherapy in patients with BRAF-mutant and BRAF wild-type advanced melanoma. Identifying a biomarker for the selection of patients benefiting most from the treatment will be crucial for further survival improvement in patients with advanced melanoma.

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