Research in castration-resistant prostate cancer: what does the future hold?

被引:0
|
作者
Macfarlane, R. J. [1 ]
Chi, K. V. [1 ,2 ,3 ]
机构
[1] BC Canc Agcy Vancouver Canc Ctr, Div Med Oncol, Vancouver, BC V5Z 4E6, Canada
[2] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[3] Univ British Columbia, Dept Urol Sci, Vancouver, BC V5Z 1M9, Canada
关键词
Castration-resistant prostate cancer; novel therapy; targeted therapy; MITOXANTRONE PLUS PREDNISONE; ANDROGEN-RESPONSIVE GENES; PHASE-I; CONTROLLED-TRIAL; CELLULAR IMMUNOTHERAPY; HORMONE; CLUSTERIN; DOCETAXEL; ATRASENTAN; RAPAMYCIN;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer (PCa) is the most common non-skin cancer diagnosed in North America, and it affects 1 in 6 men. Patients with recurrent or metastatic PCa will inevitably develop castration-resistant disease after an initial period of hormone responsiveness. The standard first-line treatment for men with castration-resistant PCa (CRPC) is docetaxel, but further treatment options are limited. This review summarizes the research being conducted in CRPC, with specific regard to immunotherapy and to novel targeted therapies directed against the androgen axis, vascular endothelial growth factor, chaperone proteins, the phosphoinositide 3 kinase/Akt/phosphatase and tensin homolog/mammalian target of rapamycin pathway, and endothelin-1.
引用
收藏
页码:S80 / S86
页数:7
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