Targeted therapy for non-small-cell lung cancer: past, present and future

被引:5
|
作者
Forde, Patrick M. [1 ]
Ettinger, David S. [2 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Lung Canc Res Program, Baltimore, MD 21287 USA
[2] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD 21287 USA
关键词
ALK; crizotinib; EGFR; epigenetic; erlotinib; immune checkpoint; non-small-cell lung cancer; PD1; targeted therapy; VEGF; PHASE-III TRIAL; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITOR; CISPLATIN PLUS GEMCITABINE; PLACEBO-CONTROLLED TRIAL; GENE COPY NUMBER; DOUBLE-BLIND; 1ST-LINE TREATMENT; OPEN-LABEL; STANDARD CHEMOTHERAPY;
D O I
10.1586/ERA.13.47
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapy for advanced non-small-cell lung cancer has developed significantly with new awareness of histologic subtype as an important factor in guiding treatment and the development of targeted agents for molecular subgroups harboring critical mutations that spur on cancer growth. In this comprehensive review, we look back at developments in targeted therapy for advanced non-small-cell lung cancer, reviewing in detail efforts, both successful and in some cases less so, to target EGFR, VEGF and ALK. This review provides an overview of where the field stands at present and the areas we feel are most likely to provide challenges and potential successes in the next 5 years including immune checkpoint inhibition, epigenetic therapy and driver mutation targeting.
引用
收藏
页码:745 / 758
页数:14
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