a Unit of Melanoma, Cancer Immunotherapy and Development Therapeutics , Istituto Nazionale Tumori IRCCS Fondazione G. Pascale , Napoli , Italy.
Expert Rev Clin Pharmacol. 2019 Mar;12(3):259-266. doi: 10.1080/17512433.2019.1570847. Epub 2019 Jan 24.
Combination treatment with a BRAF inhibitor and MEK inhibitor is the standard of care for patients with advanced BRAF mutation-positive melanoma. With the currently available combinations of dabrafenib plus trametinib and vemurafenib plus cobimetinib, median progression-free survival (PFS) of over 12 months has been achieved. However, treatment resistance and disease recurrence remain a clinical challenge. Areas covered: Encorafenib in combination with bimetinib offers a new approach that may offer benefits over existing BRAF/MEK inhibitor combinations. Expert opinion: While other BRAF/MEK inhibitor combinations have achieved a median overall survival (OS) of 22 months, patients with advanced BRAF mutation-positive melanoma treated with encorafenib plus binimetinib achieved a median OS of 33.6 months in the phase III COLUMBUS trial. PFS also appears to be improved with encorafenib plus binimetinib. This improved efficacy may be related to the distinct pharmacokinetics of encorafenib, with prolonged binding to the target molecule providing greater BRAF inhibition and increased potency compared with other drugs in the same class. Increased specificity of encorafenib may also result in better tolerability with less off-target effects, including reduced occurrence of pyrexia and photosensitivity. Encorafenib plus binimetinib seems likely to emerge as a valuable therapeutic alternative to established BRAF/MEK inhibitor combinations.
联合 BRAF 抑制剂和 MEK 抑制剂治疗是晚期 BRAF 突变阳性黑色素瘤患者的标准治疗方法。目前已有达拉非尼联合曲美替尼和维莫非尼联合考比替尼两种联合用药方案,其无进展生存期(PFS)超过 12 个月。然而,治疗耐药和疾病复发仍是临床面临的挑战。
恩考芬尼联合比美替尼为治疗提供了新的选择,可能优于现有的 BRAF/MEK 抑制剂联合方案。
虽然其他 BRAF/MEK 抑制剂联合方案的总生存期(OS)中位数达到 22 个月,但在 COLUMBUS Ⅲ期临床试验中,接受恩考芬尼联合比美替尼治疗的晚期 BRAF 突变阳性黑色素瘤患者的 OS 中位数达到 33.6 个月。PFS 似乎也得到了改善。这种疗效的提高可能与恩考芬尼独特的药代动力学有关,与同一类药物相比,恩考芬尼与靶分子的结合时间延长,提供了更强的 BRAF 抑制作用和更高的效力。恩考芬尼的特异性增加也可能导致更少的脱靶效应,包括发热和光敏性发生减少,从而具有更好的耐受性。恩考芬尼联合比美替尼似乎有可能成为现有 BRAF/MEK 抑制剂联合方案的有价值的治疗选择。