Evolving landscape and novel treatments in metastatic castrate-resistant prostate cancer

被引:27
|
作者
Toren, Paul J. [1 ]
Gleave, Martin E. [1 ]
机构
[1] Univ British Columbia, Fac Med, Dept Urol Sci, Vancouver, BC V5Z 1M9, Canada
关键词
prostate cancer; treatment resistance; androgen receptor antagonists; molecular targets; PHASE-II TRIAL; ANALOG IXABEPILONE BMS-247550; MITOXANTRONE PLUS PREDNISONE; ANDROGEN RECEPTOR; DOUBLE-BLIND; BONE METASTASES; SKELETAL COMPLICATIONS; INCREASED SURVIVAL; DOCETAXEL; PLACEBO;
D O I
10.1038/aja.2013.38
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Treatment options for castrate-resistant prostate cancer (CRPC) have advanced in recent years and significantly improved the outlook for patients with this aggressive and lethal disease. Further understanding of the biology of CRPC has led to several new targeted therapies and continues to emphasize the importance of androgen receptor (AR) directed therapy. The treatment landscape is rapidly changing and further biologically rationale, biomarker-based ongoing clinical trials are needed. We review the recent results of major clinical trials in CRPC. New and investigational agents now in clinical evaluation are reviewed including inhibitors of angiogenesis, microtubules, chaperones, AR and intracellular kinases, as well as immunotherapy, radiopharmaceuticals and bone-targeted agents. The recent improvement in prognosis for CRPC brings continued optimism for further improvements. Thoughtful planning of clinical trials and further understanding of the mechanisms of resistance to therapies will allow for continued progress in patient care.
引用
收藏
页码:342 / 349
页数:8
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