Eroglu Zeynep, Ribas Antoni
Moffitt Cancer Center, Tampa, FL, USA.
Department of Medicine, Division of Hematology-Oncology, UCLA, 11-934 Factor Building, 10833 Le Conte Avenue, Los Angeles, CA 90095-1782, USA.
Ther Adv Med Oncol. 2016 Jan;8(1):48-56. doi: 10.1177/1758834015616934.
Treatment with BRAF inhibitors such as vemurafenib or dabrafenib in patients with advanced BRAFV600 mutated melanoma has shown objective tumor responses in approximately half of the patients. However, the duration of responses is limited in a majority of these patients, with progression-free survival rates around 6 months due to tumor progression from development of acquired resistance. Preclinical studies have suggested that concurrent inhibition of the BRAF kinases and MEK of the mitogen-activated protein kinase (MAPK) pathway could decrease MAPK-driven acquired resistance, resulting in longer duration of responses, higher rate of tumor responses, and a decrease in the cutaneous toxicities observed from paradoxical MAPK pathway activation with BRAF inhibitor monotherapy. This review provides an overview of the currently available clinical trial data on BRAF and MEK inhibitors together and in combinations with other therapeutic agents.
在晚期BRAFV600突变黑色素瘤患者中,使用维莫非尼或达拉非尼等BRAF抑制剂进行治疗,约半数患者出现了客观肿瘤反应。然而,这些患者中的大多数反应持续时间有限,由于获得性耐药导致肿瘤进展,无进展生存率约为6个月。临床前研究表明,同时抑制BRAF激酶和丝裂原活化蛋白激酶(MAPK)途径的MEK,可降低MAPK驱动的获得性耐药,从而延长反应持续时间、提高肿瘤反应率,并减少BRAF抑制剂单药治疗因MAPK途径反常激活所观察到的皮肤毒性。本综述概述了目前关于BRAF和MEK抑制剂联合及与其他治疗药物联合使用的临床试验数据。