Drug Resistance to EGFR Inhibitors in Lung Cancer

被引:61
|
作者
Tetsu, Osamu [1 ,2 ]
Hangauer, Matthew J. [2 ]
Phuchareon, Janyaporn [1 ,2 ]
Eisele, David W. [1 ,2 ]
McCormick, Frank [2 ]
机构
[1] Univ Calif San Francisco, Sch Med, Dept Otolaryngol Head & Neck Surg, San Francisco, CA USA
[2] Univ Calif San Francisco, Sch Med, UCSF Helen Diller Family Comprehens Canc Ctr, 1450 3rd St,HD450, San Francisco, CA 94143 USA
关键词
Non-small-cell lung cancer; Epidermal growth factor receptor; Tyrosine kinase inhibitors; Drug resistance; Cancer dormancy; Persister cells; Monotherapy; Combination therapy; Precision medicine; GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITOR; PHASE-II TRIAL; ACQUIRED-RESISTANCE; TARGETED THERAPY; T790M MUTATION; AUTOCRINE ACTIVATION; 1ST-LINE TREATMENT; CLINICAL-RESPONSE; GENE-MUTATIONS;
D O I
10.1159/000443368
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The discovery of mutations in epidermal growth factor receptor (EGFR) has dramatically changed the treatment of patients with non-small-cell lung cancer (NSCLC), the leading cause of cancer deaths worldwide. EGFR-targeted therapies show considerable promise, but drug resistance has become a substantial issue. Methods: We reviewed the literature to provide an overview of the drug resistance to EGFR tyrosine kinase inhibitors (TKIs) in NSCLC. Results: The mechanisms causing primary, acquired and persistent drug resistance to TKIs vary. Researchers and clinicians, who have used study findings to develop more effective therapeutic approaches, have found that the sequential use of single agents presents a formidable challenge, suggesting that multidrug combinations must be considered. Conclusions: In the era of precision medicine, oncologists should promptly obtain an accurate diagnosis of drug resistance in each patient to be able to design the most relevant combination therapy to overcome patient-specific drug resistance. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:223 / 235
页数:13
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