Anti-EGF receptor therapy

被引:14
作者
Blackledge, G
Averbuch, S
Kay, A
Barton, J
机构
[1] AstraZeneca, Macclesfield SK10 4TF, Cheshire, England
[2] AstraZeneca, Wilmington, DE USA
关键词
EGFR; ZD1839; prostate cancer; hormone-resistant;
D O I
10.1038/sj.pcan.4500488
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The epidermal growth factor receptor (EGFR) signalling pathway contributes to a number of processes important to tumour progression, including cell proliferation, apoptosis, angiogenesis and metastatic spread. EGFR signalling is thought to be an important cell survival mechanism in hormone-resistant prostate cancer. ZD1839 ('Iressa') is an orally active, selective EGFR-tyrosine kinase inhibitor (EGFR-TKI) which blocks signal transduction pathways implicated in promoting cancer growth. In preclinical studies, ZD1839 alone, and in combination with cytotoxic agents, produced reversible growth inhibition and growth delay in a wide range of tumour cell lines and human tumour xenografts. Preliminary results from phase I trials in patients with advanced disease suggest that ZD1839 has an acceptable tolerability profile and promising clinical efficacy in patients with a variety of tumour types, including hormone-resistant prostate cancer, where new treatment strategies are needed.
引用
收藏
页码:296 / 302
页数:7
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