Spagnolo Francesco, Ghiorzo Paola, Queirolo Paola
Department of Plastic and Reconstructive Surgery - IRCCS Azienda Ospedaliera Universitaria San Martino - IST - Istituto Nazionale per la Ricerca sul Cancro - Genova, Italy.
Genetics of rare cancers, Department of Internal Medicine and Medical Specialties (DiMI), University of Genoa, Genova, Italy. IRCCS Azienda Ospedaliera Universitaria San Martino IST, Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
Oncotarget. 2014 Nov 15;5(21):10206-21. doi: 10.18632/oncotarget.2602.
Almost 50% of metastatic melanoma patients harbor a BRAF(V600) mutation and the introduction of BRAF inhibitors has improved their treatment options. BRAF inhibitors vemurafenib and dabrafenib achieved improved overall survival over chemotherapy and have been approved for the treatment of BRAF-mutated metastatic melanoma. However, most patients develop mechanisms of acquired resistance and about 15% of them do not achieve tumor regression at all, due to intrinsic resistance to therapy. Moreover, early adaptive responses limit the initial efficacy of BRAF inhibition, leading mostly to incomplete responses that may favor the selection of a sub-population of resistant clones and the acquisition of alterations that cause tumor regrowth and progressive disease. The purpose of this paper is to review the mechanisms of resistance to therapy with BRAF inhibitors and to discuss the strategies to overcome them based on pre-clinical and clinical evidences.
近50%的转移性黑色素瘤患者存在BRAF(V600)突变,BRAF抑制剂的引入改善了他们的治疗选择。BRAF抑制剂维莫非尼和达拉非尼相较于化疗提高了总生存率,并已被批准用于治疗BRAF突变的转移性黑色素瘤。然而,大多数患者会产生获得性耐药机制,约15%的患者由于对治疗的固有耐药性根本无法实现肿瘤消退。此外,早期适应性反应限制了BRAF抑制的初始疗效,大多导致反应不完全,这可能有利于耐药克隆亚群的选择以及导致肿瘤再生和疾病进展的改变的获得。本文的目的是回顾BRAF抑制剂治疗耐药的机制,并根据临床前和临床证据讨论克服这些耐药机制的策略。