Recent Advances in Targeting ROS1 in Lung Cancer

被引:204
作者
Lin, Jessica J. [1 ]
Shaw, Alice T. [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc, 32 Fruit St, Boston, MA 02114 USA
关键词
ROS1; rearrangement; Non-small cell lung cancer; Crizotinib; inhibitor; Resistance; ANAPLASTIC LYMPHOMA KINASE; TYROSINE KINASE; OPEN-LABEL; ALK REARRANGEMENTS; C-ROS; INHIBITOR SENSITIVITY; CRIZOTINIB RESISTANCE; ACQUIRED-RESISTANCE; FUSION VARIANT; HUMAN C-ROS-1;
D O I
10.1016/j.jtho.2017.08.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ROS1 is a validated therapeutic target in NSCLC. In a phase I study, the multitargeted MET proto-oncogene, receptor tyrosine kinase/anaplastic lymphoma kinase/ROS1 inhibitor crizotinib demonstrated remarkable efficacy in ROS1-rearranged NSCLCs and consequently gained approval by the United States Food and Drug Administration and by the European Medicines Agency in 2016. However, similar to other oncogene-driven lung cancers, ROS1-rearranged lung cancers treated with crizotinib eventually acquire resistance, leading to disease relapse. Novel ROS1 inhibitors and therapeutic strategies are therefore needed. Insights into the mechanisms of resistance to ROS1-directed tyrosine kinase inhibitors are now beginning to emerge and are helping to guide the development of new ROS1 inhibitors. This review discusses the biology and diagnosis of ROS1-rearranged NSCLC, and current and emerging treatment options for this disease. Future challenges in the field are highlighted. (C) 2017 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1611 / 1625
页数:15
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