Emerging therapeutic approaches in the management of metastatic castration-resistant prostate cancer

被引:18
作者
Antonarakis, E. S. [1 ]
Armstrong, A. J. [2 ,3 ,4 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Prostate Canc Res Program, Baltimore, MD 21231 USA
[2] Duke Univ, Dept Med, Duke Canc Inst, Durham, NC USA
[3] Duke Univ, Dept Surg, Duke Canc Inst, Durham, NC USA
[4] Duke Univ, Duke Prostate Ctr, Durham, NC USA
关键词
castrate-resistant prostate cancer; novel therapies; clinical trials; drug development; RECEPTOR TYROSINE KINASE; CYTOTOXIC T-LYMPHOCYTE; PHASE-II TRIAL; ANDROGEN RECEPTOR; ANTITUMOR-ACTIVITY; MAMMALIAN TARGET; POLY(ADP-RIBOSE) POLYMERASE; FIGITUMUMAB CP-751,871; INHIBITS GROWTH; CTLA-4; BLOCKADE;
D O I
10.1038/pcan.2011.24
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Although treatment options for men with castration-resistant prostate cancer (CRPC) have improved with the recent and anticipated approvals of novel immunotherapeutic, hormonal, chemotherapeutic and bone-targeted agents, clinical benefit with these systemic therapies is transient and survival times remain unacceptably short. Thus, we devote the second section of this two-part review to discussing emerging therapeutic paradigms and research strategies that are entering phase II and III clinical testing for men with metastatic CRPC. We will discuss a range of emerging hormonal, immunomodulatory, antiangiogenic, epigenetic and cell survival pathway inhibitors in current clinical trials, with an emphasis on how these therapies may complement our existing treatment options. Prostate Cancer and Prostatic Diseases (2011) 14, 206-218; doi:10.1038/pcan.2011.24; published online 17 May 2011
引用
收藏
页码:206 / 218
页数:13
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