Clinical experience with gefitinib: An update

被引:55
作者
Cappuzzo, F
Finocchiaro, G
Metro, G
Bartolini, S
Magrini, E
Cancellieri, A
Trisolini, R
Castaldini, L
Tallini, G
Crino, L
机构
[1] Bellaria Hosp, Dept Med Oncol, I-40139 Bologna, Italy
[2] Bellaria Hosp, Dept Pathol, I-40139 Bologna, Italy
[3] Bellaria Hosp, Dept Radiol, I-40139 Bologna, Italy
[4] Maggiore Hosp, Dept Pathol, Bologna, Italy
[5] Maggiore Hosp, Dept Pneumol, Bologna, Italy
关键词
EGFR; tyrosine kinase inhibitor; gefitinib; non-small cell lung cancer;
D O I
10.1016/j.critrevonc.2005.08.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gefitinib is an orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that blocks signal transduction pathways involved in cell proliferation. This drug demonstrated impressive and durable responses in patients with heavily pretreated non-small cell lung cancer (NSCLC). In two large phase II trials, responses were observed in 9-19% of unselected patients, along with symptom improvement and benefit in quality of life. Biological mechanisms underlying TKI sensitivity have recently been discovered. There is evidence that specific EGFR gene mutations and/or amplification confer a particularly sensitive phenotype, especially in individuals with tumors demonstrating activation of the anti-apoptotic protein Akt. However, in all so far conducted clinical trials, no patient selection has been made, providing a logical explanation for the negative results observed in large phase III studies. In the present review, we will summarize the results observed in clinical trials with gefitinib. We will present results obtained in NSCLC and in other solid tumor, focusing on biological and clinical markers predicting drug sensitivity. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:31 / 45
页数:15
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