Management of Castrate Resistant Prostate Cancer-Recent Advances and Optimal Sequence of Treatments

被引:15
作者
Zhang, Tian Yi [1 ]
Agarwal, Neeraj [1 ]
Sonpavde, Guru [2 ]
DiLorenzo, Giuseppe [3 ]
Bellmunt, Joaquim [4 ]
Vogelzang, Nicholas J. [5 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[2] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL 35294 USA
[3] Univ Naples Federico II, Naples, Italy
[4] Univ Hosp Mar IMIM, Barcelona, Spain
[5] Comprehens Canc Ctr Nevada, Las Vegas, NV USA
关键词
Metastatic castration resistant prostate cancer; Sipuleucel-T; Androgen axis inhibitors; Abiraterone; Enzalutamide; Cabazitaxel; Alpharadin (Radium-223); Agents in phase 3 trials; Optimal sequencing of novel agents; PHASE-II; ABIRATERONE ACETATE; INCREASED SURVIVAL; CONTROLLED-TRIAL; DOUBLE-BLIND; PREDNISONE; DOCETAXEL; MITOXANTRONE; TASQUINIMOD; IMMUNOTHERAPY;
D O I
10.1007/s11934-013-0322-0
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Until 2010, chemotherapy with docetaxel was the only approved agent for treatment of metastatic castrate resistant prostate cancer (mCRPC). Since then, the therapeutic landscape of mCRPC has changed rapidly. Multiple novel agents have received regulatory approval after demonstrating improved overall survival in separate randomized Phase 3 studies. These include immunotherapeutic agent sipuleucel-T, androgen axis inhibitors abiraterone and enzalutamide, and a novel microtubule inhibitor cabazitaxel. More recently, radium-223, a bone-targeting alpha emitting radiopharmaceutical, was reported to improve skeletal related events, as well as overall survival in a Phase 3 randomized study. Additionally, there are several promising agents in the advanced stages of clinical development. Here, we describe the agents recently shown to improve overall survival, and those that have reached the advanced stages of development in Phase 3 clinical trials. We will also propose a strategy for optimal sequencing of these agents in the treatment of mCRPC.
引用
收藏
页码:174 / 183
页数:10
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