Bennati Chiara, Paglialunga Luca, Ricciuti Biagio, Metro Giulio, Marcomigni Luca, Gili Alessio, Crinò Lucio
Department of Medical Oncology, S Maria della Misericordia Hospital, Perugia/Italy.
Department of Experimental Medicine, S Maria della Misericordia Hospital, Perugia/Italy.
Lung Cancer Manag. 2016 Jun;5(2):79-90. doi: 10.2217/lmt-2016-0005. Epub 2016 Jun 23.
The advent of molecular therapy targeting specific driver oncogenes has dramatically changed the prognosis of a subset of NSCLC, dilating survival and improving the quality of life of patients with advanced disease. Two of the major targets for treatment with receptor TKIs are the activated mutated forms of the and the gene fusions. In advanced NSCLC patients harboring mutations or rearrangements, the use of TKIs in the first-line setting, have provided unexpected large progression-free survival and overall survival benefits, compared with cytotoxic chemotherapy. However, despite initial responses and durable remissions, the development of resistance inevitably leads to treatment failure. The aim of this review is to discuss the treatment strategy currently used for tumors harboring these two genetic targets and to focus on what will be available in clinical practice in the near future.
针对特定驱动癌基因的分子疗法的出现极大地改变了一部分非小细胞肺癌(NSCLC)的预后,延长了生存期并改善了晚期疾病患者的生活质量。受体酪氨酸激酶抑制剂(TKIs)治疗的两个主要靶点是激活的突变形式的[具体基因1]和[具体基因2]基因融合。在携带[具体基因1]突变或[具体基因2]重排的晚期NSCLC患者中,与细胞毒性化疗相比,在一线治疗中使用TKIs已带来了意想不到的长无进展生存期和总生存期益处。然而,尽管有初始反应和持久缓解,但耐药性的出现不可避免地导致治疗失败。本综述的目的是讨论目前用于具有这两个基因靶点的肿瘤的治疗策略,并关注在不久的将来临床实践中将可用的治疗方法。