Changing Therapeutic Paradigms in Castrate-Resistant Prostate Cancer

被引:14
|
作者
Zivi, Andrea
Massard, Christophe
De-Bono, Johann
机构
[1] Royal Marsden NHS Fdn Trust, Sutton SM2 5PT, Surrey, England
[2] Inst Canc Res, Sutton SM2 5NG, Surrey, England
关键词
Abiraterone; Androgen receptor; CRPC; MDV-3100; INHIBITOR ABIRATERONE ACETATE; I CLINICAL-TRIAL; STEROIDAL INHIBITORS; ANTITUMOR-ACTIVITY; ANDROGEN RECEPTOR; PLUS PREDNISONE; DOCETAXEL; CYP17; ERG; ANTIANDROGEN;
D O I
10.3816/CGC.2010.n.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer is the most common cancer, and the second leading cause of death from cancer, in males in most Western countries. Advanced prostate cancer is initially sensitive to androgen deprivation therapy, but usually progresses to the castration-resistant state. There is now incontrovertible evidence that castration-resistant prostate cancer (CRPC) remains hormone driven, with intratumoral steroid synthesis fueling tumor growth. Several novel agents targeted androgen receptor signaling are currently being evaluated including abiraterone and MDV3100. Recent results of the phase Ill trial of abiraterone acetate in post-docetaxel patients has shown an overall survival benefit in advanced CRPC. This new treatment is likely to become a new standard of care for patients with metastatic CRPC.
引用
收藏
页码:17 / 22
页数:6
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