埃罗替尼
吉非替尼
医学
肺癌
肿瘤科
酪氨酸激酶
酪氨酸激酶抑制剂
内科学
盐酸厄洛替尼
临床试验
表皮生长因子受体
药理学
癌症
受体
作者
Antonio Passaro,Daniele Adami,Alessia Pochesci,Enrico Cortesi
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2014-05-31
卷期号:14 (5): 646-650
被引量:9
标识
DOI:10.2174/187152061405140501101624
摘要
Erlotinib and gefitinib are tyrosine kinase inhibitors (TKI) associated with the EGFR, which is involved in cell proliferation, growth, migration, invasion and survival, and has been found to be overexpressed in non-small-cell lung cancer. Erlotinib was the first target agent approved for the treatment of NSCLC in second- and third line, in patients unselected for EGFR mutations; gefitinib was the first EGFR tyrosine kinase inhibitor approved for the treatment of NSCLC in all lines of setting in patients harbouring EGFR mutations. In elderly patients, with a poor prognosis, and different co-morbidities, erlotinib and gefitinib could be considered as valid therapeutic options. This paper reviews the role of both drugs, in the management of elderly patients affected by advanced NSCLC based on an update analysis of randomised and non-randomised clinical trials. Keywords: EGFR, elderly, erlotinib, gefitinib, non-small-cell lung cancer, tyrosine kinase inhibitor.
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