New developments in castrate-resistant prostate cancer

被引:31
|
作者
Shore, N. [1 ]
Mason, M. [2 ]
de Reijke, Th. M. [3 ]
机构
[1] Atlantic Urol Clin, Carolina Urol Res Ctr, Myrtle Beach, SC 29572 USA
[2] Cardiff Univ, Inst Canc & Genet, Velindre Hosp, Cardiff, S Glam, Wales
[3] Univ Amsterdam, Dept Urol, Amsterdam, Netherlands
关键词
anti-androgens; CRPC; cytotoxic therapy; immunotherapy; secondary hormone therapy; targeted therapy; PHASE-II TRIAL; CIRCULATING TUMOR-CELLS; IMMUNE-SYSTEM; THERAPY; DOCETAXEL; SURVIVAL; DIETHYLSTILBESTROL; IMMUNOTHERAPY; MITOXANTRONE; COMBINATION;
D O I
10.1111/j.1464-410X.2012.11217.x
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
1002 ; 100201 ;
摘要
Castrate-resistant prostate cancer (CRPC) occurs when disease progresses in the presence of castrate levels of androgens and remains sensitive to further hormonal manipulation. For many years the treatment of CRPC was limited to the use of docetaxel for metastatic disease. However, this has recently changed with the approval of several new agents. Sipuleucel-T, an immunotherapeutic vaccine, is now available in the US for patients with non-metastatic CRPC and abiraterone, an oral enzyme inhibitor of androgen biosynthesis, as well as cabazitaxel, a cytotoxic chemotherapeutic, have been approved for the treatment of metastatic CRPC. Also, denosumab, a subcutaneous antibody, is now an option for the treatment of patients with CRPC with bone metastases, in addition to zoledronic acid, an intravenous bisphosphonate. Further treatment advances for metastatic CRPC therapeutics are in late stage phase III development. These include therapies affecting the androgen receptor (MDV3100) as well as additional immune-based therapeutics, PROSTVAC and ipilimumab. A broad range of agents is also emerging under the term targeted therapies. The endothelin-A receptor antagonist zibotentan, the tyrosine kinase inhibitors dasatinib, sorafenib and cabozantinib, the anti-angiogenic agent aflibercept, and the clusterin inhibitor custirsen, are all currently being tested for efficacy in metastatic CRPC. The mechanism of action of these and other promising agents are discussed alongside current therapeutic options and their potential place in the treatment landscape for CRPC is considered.
引用
收藏
页码:22 / 32
页数:11
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