Farago Anna F, Azzoli Christopher G
Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Transl Lung Cancer Res. 2017 Oct;6(5):550-559. doi: 10.21037/tlcr.2017.08.02.
The discovery of gene rearrangements involving the receptor tyrosine kinase genes and has revolutionized management of the subset of non-small cell lung cancers characterized by these alterations. The oncogenic fusion proteins expressed in these tumors drive cancer cell growth and survival, and targeted inhibition of this signaling can lead to dramatic and durable responses in patients. While the best characterized gene fusions in non-small cell lung cancer (NSCLC) involve and , fusions involving other kinases including , , and are now established as additional targetable drivers. Here we review data supporting the roles of these fusions as oncogenic drivers, and the potential for targeting these fusions for improved clinical outcomes. These discoveries should encourage multiplexed molecular profiling of lung cancers using next-generation platforms which identify these gene fusions in order to expand treatment options for patients.
涉及受体酪氨酸激酶基因的基因重排的发现,彻底改变了以这些改变为特征的非小细胞肺癌亚组的治疗方式。这些肿瘤中表达的致癌融合蛋白驱动癌细胞的生长和存活,对这种信号传导的靶向抑制可使患者产生显著且持久的反应。虽然非小细胞肺癌(NSCLC)中特征最明确的基因融合涉及 和 ,但涉及其他激酶(包括 、 、 和 )的融合现在已被确认为其他可靶向的驱动因素。在此,我们回顾支持这些融合作为致癌驱动因素作用的数据,以及靶向这些融合以改善临床结果的潜力。这些发现应鼓励使用下一代平台对肺癌进行多重分子分析,以识别这些基因融合,从而为患者扩大治疗选择。