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
相关论文
共 52 条
[1]   GROWTH-FACTORS AND CANCER [J].
AARONSON, SA .
SCIENCE, 1991, 254 (5035) :1146-1153
[2]  
Akimoto T, 1999, CLIN CANCER RES, V5, P2884
[3]  
BASELGA J, 1999, AACR NCI EORTC WASH
[4]  
BASELGA J, 2000, P AN M AM SOC CLIN, V19, pA686
[5]  
BRASS AL, 1995, CANCER RES, V55, P3197
[6]  
BUDILLON A, 2000, P AM ASSOC CANC RES, V41, pA4910
[7]  
CHAN KC, 2000, AM ASS CANC RES SAN
[8]  
Chen Z, 2000, ANTICANCER RES, V20, P899
[9]  
Ciardiello F, 2000, CLIN CANCER RES, V6, P2053
[10]  
COX G, 2000, P AN M AM SOC CLIN, V19, P482