Treatment of metastatic castration-resistant prostate cancer (mCRPC) with enzalutamide

被引:9
|
作者
Baciarello, Giulia [1 ]
Sternberg, Cora N. [1 ]
机构
[1] San Camillo & Forlanini Hosp, Dept Med Oncol, Padigl Flajani,Circonvallaz Gianicolense 87, I-00152 Rome, Italy
关键词
Enzalutamide; Antiandrogen therapy; Cross resistance; Primary resistance; Combination therapy; ANDROGEN-RECEPTOR GENE; QUALITY-OF-LIFE; ANTIANDROGEN WITHDRAWAL SYNDROME; ABIRATERONE ACETATE; GLUCOCORTICOID-RECEPTOR; ANTITUMOR-ACTIVITY; DOUBLE-BLIND; CLINICAL ACTIVITY; CONFERS RESISTANCE; INCREASED SURVIVAL;
D O I
10.1016/j.critrevonc.2016.07.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer is initially responsive to androgen deprivation therapy, but most patients eventually develop castration-resistant disease. Enzalutamide is an androgen receptor (AR) inhibitor that targets several steps in the AR signaling pathway and has shown significant efficacy in the treatment of metastatic castration-resistant prostate cancer in patients with or without prior chemotherapy. To provide optimal treatment, it is important to understand the implications of enzalutamide use in the context of other therapies, as recent findings have suggested cross-resistance occurs between and within drug classes. Mutations and splice variants of AR also impact the course of prostate cancer. Future strategies involving enzalutamide should account for previous exposure to taxanes or antiandrogen therapies and the presence of AR variants that could affect efficacy. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:14 / 24
页数:11
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