Chu Quincy S
Division of Medical Oncology, Department of Oncology, Cross Cancer Institute, University of Alberta, 11560 University Avenue, Edmonton, Alberta, T6G 1Z2, Canada.
Ther Adv Med Oncol. 2020 Jan 23;12:1758835919895756. doi: 10.1177/1758835919895756. eCollection 2020.
The identification of driver mutations in epidermal growth factor receptor, anaplastic lymphoma kinase, the and genes and subsequent successful clinical development of kinase inhibitors not only significantly improves clinical outcomes but also facilitates the discovery of other novel driver mutations in non-small cell lung cancer. These driver mutations can be categorized into mutations in or near the kinase domain, gene amplification or fusion. In this review, V600E, and exon 20 mutation, -4, , , , , , and gene aberration and their therapeutics will be discussed.
在表皮生长因子受体、间变性淋巴瘤激酶、 以及 基因中鉴定驱动突变,以及随后激酶抑制剂的成功临床开发,不仅显著改善了临床结果,还促进了非小细胞肺癌中其他新型驱动突变的发现。这些驱动突变可分为激酶结构域内或附近的突变、基因扩增或融合。在本综述中,将讨论V600E、 以及 外显子20突变、-4、 、 、 、 、 以及 基因畸变及其治疗方法。