Overcoming Molecular Mechanisms of Resistance to First-Generation Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors

被引:25
作者
Bar, Jair [1 ,2 ]
Onn, Amir [1 ]
机构
[1] Chaim Sheba Med Ctr, Div Oncol, IL-52621 Tel Hashomer, Israel
[2] Ottawa Hosp Canc Ctr, Div Med Oncol, Ottawa, ON, Canada
关键词
EGFR; Irreversible tyrosine kinase inhibitors; NSCLC; Resistance; Reversible tyrosine kinase inhibitors; CELL LUNG-CANCER; PHASE-II TRIAL; PREVIOUSLY TREATED PATIENTS; ACQUIRED-RESISTANCE; EGF RECEPTOR; GEFITINIB RESISTANCE; T790M MUTATIONS; KRAS MUTATION; ERLOTINIB; SENSITIVITY;
D O I
10.1016/j.cllc.2011.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) gefitinib and erlotinib have provided substantial benefits to patients with advanced non-small cell lung cancer (NSCLC). However resistance to these agents has emerged as a significant clinical issue; most patients who initially respond to treatment eventually experience relapse. The mechanisms underlying gefitinib and erlotinib resistance are multifactorial and several have been described. Clearly there is a need for novel and more effective therapies that can overcome resistance to the currently available TKIs. Several agents are in clinical development, including irreversible EGFR TKIs, inhibitors of the MET pathway, and others. In this review we discuss the various underlying mechanisms of gefitinib and erlotinib resistance and highlight the agents currently in clinical development that may have potential for overcoming this resistance.
引用
收藏
页码:267 / 279
页数:13
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