Rational, biologically based treatment of EGFR-mutant non-small-cell lung cancer

被引:975
作者
Pao, William [1 ]
Chmielecki, Juliann [2 ]
机构
[1] Vanderbilt Ingram Canc Ctr, Dept Med, Nashville, TN 37232 USA
[2] Weill Cornell Grad Sch Med Sci, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITOR; PREVIOUSLY TREATED PATIENTS; PHASE-III TRIAL; GENE COPY NUMBER; NONSMALL-CELL; ACQUIRED-RESISTANCE; T790M MUTATION; BCR-ABL; INCREASED SENSITIVITY;
D O I
10.1038/nrc2947
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Epidermal growth factor receptor (EGFR)-mutant non-small-cell lung cancer (NSCLC) was first recognized in 2004 as a distinct, clinically relevant molecular subset of lung cancer. The disease has been the subject of intensive research at both the basic scientific and clinical levels, becoming a paradigm for how to understand and treat oncogene-driven carcinomas. Although patients with EGFR-mutant tumours have increased sensitivity to tyrosine kinase inhibitors (TKIs), primary and acquired resistance to these agents remains a major clinical problem. This Review summarizes recent developments aimed at treating and ultimately curing the disease.
引用
收藏
页码:760 / 774
页数:15
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