Metastatic castration-resistant prostate cancer: new therapies, novel combination strategies and implications for immunotherapy

被引:36
|
作者
Drake, C. G. [1 ]
Sharma, P. [2 ]
Gerritsen, W. [3 ]
机构
[1] Johns Hopkins Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, 1650 Orleans St CRB 410, Baltimore, MD 21231 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[3] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, NL-6525 ED Nijmegen, Netherlands
关键词
androgen ablation; chemotherapy; immunotherapy; post-docetaxel; prostate cancer; radiotherapy; T-CELL RESPONSES; IMMUNE-RESPONSE; CTLA-4; BLOCKADE; INCREASED SURVIVAL; RECENT SUCCESSES; CLINICAL-TRIALS; LOCAL RADIATION; TUMOR-CELLS; OPEN-LABEL; PHASE-II;
D O I
10.1038/onc.2013.497
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For the past decade, docetaxel has remained the global standard of care for frontline treatment of metastatic castration-resistant prostate cancer (mCRPC). Until recently, there were limited options for patients with mCRPC following docetaxel failure or resistance, but now the approved treatment choices for these patients have expanded to include abiraterone acetate, cabazitaxel and enzalutamide. Additionally, the radioactive therapeutic agent radium-223 dichloride has been recently approved in patients with CRPC with bone metastases. Although each of these agents has been shown to convey significant survival benefit as a monotherapy, preclinical findings suggest that combining such innovative strategies with traditional treatments may achieve additive or synergistic effects, further augmenting patient benefit. This review will discuss the transformation of the post-docetaxel space in mCRPC, highlighting the spectrum of newly approved agents in this setting in the USA and the European Union, as well as summarizing treatments with non-chemotherapeutic mechanisms of action that have demonstrated promising results in recent phase 3 trials. Lastly, this review will address the potential of combinatorial regimens in mCRPC, including the pairing of novel immunotherapeutic approaches with chemotherapy, radiotherapy or androgen ablation.
引用
收藏
页码:5053 / 5064
页数:12
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