Melanoma Unit, Hospital Vall d'Hebrón, Barcelona, Spain.
Ann Transl Med. 2015 Sep;3(15):207. doi: 10.3978/j.issn.2305-5839.2015.05.13.
Selective inhibition of the mitogen activated protein kinase (MAPK) pathway with either BRAF or MEK inhibition has emerged as the key component for the treatment of BRAF-mutant metastatic melanoma. New evidence from several phase III trials suggests that the combination of BRAF and MEK inhibitors improves tumor response rate and progression-free survival (PFS). Some of the serious adverse events, in particular, the incidence of cutaneous squamous cell carcinoma seen with the monotherapy treatment with a BRAF inhibitor are attenuated with combination therapy, whereas milder side effects such as pyrexia can be more common with combination therapy. Although dose reductions and dose interruptions are slightly more common with combination therapy, overall data supports the notion that combination therapy is safe and improves the outcomes for metastatic melanoma patients compared to single agent BRAF inhibitors.
选择性抑制丝裂原活化蛋白激酶 (MAPK) 通路,无论是使用 BRAF 抑制剂还是 MEK 抑制剂,都已成为治疗 BRAF 突变型转移性黑色素瘤的关键组成部分。来自几项 III 期试验的新证据表明,BRAF 和 MEK 抑制剂的联合治疗可提高肿瘤缓解率和无进展生存期 (PFS)。一些严重的不良反应,特别是单独使用 BRAF 抑制剂治疗时出现的皮肤鳞状细胞癌的发生率,随着联合治疗而减轻,而联合治疗时更常见的是较轻的副作用,如发热。虽然联合治疗时剂量减少和中断更常见,但总体数据支持联合治疗是安全的,并改善转移性黑色素瘤患者的预后,优于单一 BRAF 抑制剂。