Epidermal growth factor receptor tyrosine kinase inhibitors for non-small cell lung cancer

被引:27
|
作者
Asami, Kazuhiro [1 ]
Atagi, Shinji [1 ]
机构
[1] Natl Hosp Org Kinki Chuo Chest Med Ctr, Dept Clin Oncol, Sakai, Osaka 5918555, Japan
来源
WORLD JOURNAL OF CLINICAL ONCOLOGY | 2014年 / 5卷 / 04期
关键词
Epidermal growth factor receptor mutation; Epidermal growth factor receptor tyrosine kinase inhibitors; Non-small cell lung cancer; Secondary resistance;
D O I
10.5306/wjco.v5.i4.646
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
First-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), including gefitinib and erlotinib, have proven to be highly effective agents for advanced non-small cell lung cancer (NSCLC) in patients harboring an activating EGFR mutation such as the exon 19 deletion mutation and L858R. Although those reversible small molecular targeted agents provide a significant response and survival benefit, all responders eventually acquire resistance. Second-generation EGFR-targeting agents, such as irreversible EGFR/HER2 tyrosine kinase inhibitors and pan-HER TKIs, may improve survival further and be useful for patients who acquired resistance to first-generation EG-FR-TKIs. This review discusses novel therapeutic strategies for EGFR-mutated advanced NSCLC using first- and second-generation EGFR-TKIs. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:646 / 659
页数:14
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