Phase III data for abiraterone in an evolving landscape for castration-resistant prostate cancer

被引:10
|
作者
Pal, Sumanta Kumar [1 ]
Sartor, Oliver [2 ,3 ]
机构
[1] City Hope Comprehens Canc Ctr, Dept Med Oncol & Expt Therapeut, Div Genitourinary Malignancies, Los Angeles, CA USA
[2] Tulane Univ, Sch Med, Dept Urol, New Orleans, LA 70112 USA
[3] Tulane Univ, Sch Med, Dept Med, New Orleans, LA 70112 USA
关键词
Abiraterone; Phase III; ESMO; 2010; European Society for Medical Oncology; CYP17; Survival data; MDV3100; Cabazitaxel; Prostate cancer; Castration-resistant prostate cancer; CRPC; ANTITUMOR-ACTIVITY; PLUS PREDNISONE; DOCETAXEL; CYP17; MITOXANTRONE; ACETATE; INHIBITOR;
D O I
10.1016/j.maturitas.2010.10.009
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
At the 2010 meeting of the European Society for Medical Oncology (ESMO), a landmark development in prostate cancer therapy was unveiled. In a phase III study, the CYP17 inhibitor abiraterone yielded a survival advantage over placebo in patients with metastatic castration-resistant prostate cancer (mCRPC) who had progressed despite prior docetaxel therapy. The data for abiraterone follow the publication of successful phase III studies earlier this year supporting two mechanistically distinct agents namely, the novel taxane cabazitaxel and the autologous dendritic cell vaccine sipuleucel-T. A challenge that lies ahead for the scientific community is to discern the appropriate positioning of abiraterone in an increasingly crowded therapeutic landscape. Several ongoing trials are examining the agent in earlier settings (i.e., a phase III in mCRPC pre-docetaxel, and smaller studies in combination with radiation therapy or as neoadjuvant pre-surgery for localized disease). Herein, several potential strategies for abiraterone are presented to clarify the clinical utilization of this agent in the future. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:103 / 105
页数:3
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