Advancing therapies in metastatic castration-resistant prostate cancer

被引:24
作者
Baciarello, Giulia [1 ]
Gizzi, Marco [2 ,3 ]
Fizazi, Karim [1 ]
机构
[1] Univ Paris Sud, Inst Gustave Roussy, Dept Med Oncol, Villejuif, France
[2] Grand Hop Charleroi, Serv Oncol, Brussels, Belgium
[3] Clin Univ St Luc, Brussels, Belgium
关键词
Castration resistant; prostate cancer; PARP inhibitors; immunotherapy; prostate specific membrane antigen; PI3K pathways inhibitors; OPEN-LABEL; POLY(ADP-RIBOSE) POLYMERASE; BRCA MUTATION; INCREASED SURVIVAL; DOSE-ESCALATION; SOLID TUMORS; PHASE-I; DOCETAXEL; MULTICENTER; CHEMOTHERAPY;
D O I
10.1080/14656566.2018.1527312
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Prostate cancer is the second most common cause of cancer worldwide and is the most frequently detected cancer in the European Union in men over 50 years of age. Androgen deprivation therapy remains the cornerstone of treatment for recurrent or metastatic disease. Unfortunately, nearly all patients will develop resistance to androgen blockade leading to castration-resistant prostate cancer (CRPC). Over the last 10 years, new treatments have dramatically improved overall survival of men with mCRPC. Current therapies are based on AR-axis inhibitors and taxane-based chemotherapies, as well as radiopharmaceuticals and Sipuleucel T. Areas covered: The authors provide a review of the current field of systemic therapy in metastatic CRPC. This is followed by an in-depth analysis of recent developments in treatment, and the biological rationale behind these therapies. Expert opinion: Since several trials with docetaxel or novel hormonal agents showed improvement in overall survival in metastatic castration-sensitive prostate cancer, as well as in non-metastatic castration-resistant patients, it is expected that a growing subgroup of patients will be exposed earlier to chemotherapy and to AR targeted agents. It becomes then fundamental to find novel strategies to overcome drug resistance and further improve survival.
引用
收藏
页码:1797 / 1804
页数:8
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