Metastatic castration-resistant prostate cancer (CRPC): preclinical and clinical evidence for the sequential use of novel therapeutics

被引:51
作者
Mukherji, Deborah [1 ]
Omlin, Aurelius [2 ,3 ,4 ]
Pezaro, Carmel [2 ,3 ,4 ]
Shamseddine, Ali [1 ]
de Bono, Johann [2 ,3 ,4 ]
机构
[1] Amer Univ Beirut, Med Ctr, Dept Internal Med, Div Hematol Oncol, Beirut 11072020, Lebanon
[2] Royal Marsden NHS Fdn Trust, Prostate Canc Targeted Therapy Grp, Sutton, Surrey, England
[3] Royal Marsden NHS Fdn Trust, Drug Dev Unit, Sutton, Surrey, England
[4] Inst Canc Res, Sutton, Surrey, England
关键词
Castration-resistant prostate cancer (CRPC); Androgen receptor signaling; Abiraterone acetate; Enzalutamide; Cabazitaxel; Sequential treatment strategies; ANDROGEN RECEPTOR; ABIRATERONE ACETATE; ANTITUMOR-ACTIVITY; INCREASED SURVIVAL; CONTROLLED-TRIAL; SIPULEUCEL-T; DOCETAXEL; ENZALUTAMIDE; PREDNISONE; PLACEBO;
D O I
10.1007/s10555-013-9473-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With five novel therapies shown to improve survival in metastatic castration-resistant prostate cancer (CRPC) in the last 3 years, patients are now living longer and experiencing better quality of life. Since docetaxel became standard of care for men with symptomatic metastatic CRPC, three artificial treatment "spaces" have emerged for prostate cancer drug development: pre-docetaxel, docetaxel combinations, and following docetaxel. Multiple therapies are currently under development in both early and late stage CRPC. Additionally, the novel agents abiraterone, radium-223, cabazitaxel, and enzalutamide have all been approved in the post-docetaxel setting. Strategies for patient selection and treatment sequencing are therefore urgently required. In this comprehensive review, we will summarize the preclinical and clinical data available with regards to sequencing of the novel treatments for CRPC.
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收藏
页码:555 / 566
页数:12
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