临床试验
热休克蛋白90
医学
恶性肿瘤
药物开发
不利影响
药品
肿瘤科
药理学
内科学
重症监护医学
热休克蛋白
生物
生物化学
基因
作者
Y S Kim,Sylvia V. Alarcon,S Lee,M.-J. Lee,Giuseppe Giaccone,Len Neckers,Jane B. Trepel
标识
DOI:10.2174/156802609789895728
摘要
Twenty-five years ago the first small molecule inhibitors of Hsp90 were identified. In the intervening years there has been dramatic progress in basic scientific understanding of the Hsp90 chaperone machinery and in the role of Hsp90 in malignancy. The first-in-class Hsp90 inhibitor 17-AAG entered into Phase I clinical trials in 1999. There are now 13 Hsp90 inhibitors in clinical trial, representing multiple drug classes, and hundreds of patients have been treated in adult oncology and pediatric oncology trials. This review will provide an overview of the clinical trial results thus far. In addition, pivotal issues in further development of Hsp90 inhibitors as anticancer drugs will be discussed.
科研通智能强力驱动
Strongly Powered by AbleSci AI