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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Enzalutamide: A novel antiandrogen for patients with castrate-resistant prostate cancer
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Enzalutamide: A novel antiandrogen for patients with castrate-resistant prostate cancer

机译:Enzalutamide:针对去势抵抗性前列腺癌患者的新型抗雄激素药物

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摘要

Enzalutamide (MDV3100, Xtandi, MedivationAstellas) is an oral inhibitor of androgen receptor signaling that blocks androgen receptor interaction, inhibits translocation of the androgen receptor to the nucleus, impairs androgen receptor binding to DNA, and inhibits coactivator recruitment and receptor-mediated DNA transcription. In a phase III randomized study comparing enzalutamide with placebo inmen with progressive castration-resistant prostate cancer (CRPC) who were previously treated with docetaxel, enzalutamide showed an improvement in overall survival (18.4 vs. 13.6 months, HR, 0.63; P < 0.001). In addition, all secondary endpoints including proportion of patients with prostate-specific antigen (PSA) decline, soft-tissue response, quality-of-life response, time to PSA progression, radiographic progression-free survival, and the time to the first radiographic skeletal event all significantly favored patients treated with enzalutamide. Fatigue, diarrhea, and hot flashes were common in patients treated with enzalutamide, with seizures reported in 5 (0.6%) of the patients. Enzalutamide is a novel therapy that very potently blocks the androgen signaling pathway, which is unregulated during the development of CRPC. The preclinical studies along with the pivotal trials that led to its approval by the U.S. Food and Drug Administration (FDA) in September 2012 will be reviewed.
机译:Enzalutamide(MDV3100,Xtandi,Medivation Astellas)是雄激素受体信号传导的口服抑制剂,可阻断雄激素受体相互作用,抑制雄激素受体向核的转运,削弱雄激素受体与DNA的结合,并抑制共激活剂募集和受体介导的DNA转录。在一项Ⅲ期随机研究中,将enzalutamide与先前接受过多西他赛治疗的进展期去势抵抗性前列腺癌(CRPC)安慰剂患者进行比较,enzalutamide的总生存期有所改善(18.4 vs. 13.6个月,HR,0.63; P <0.001) 。此外,所有次要终点均包括前列腺特异性抗原(PSA)下降,软组织反应,生活质量反应,PSA进展时间,无影像学无进展生存时间和首次影像学时间的患者比例骨骼事件均显着有利于恩杂鲁胺治疗的患者。恩杂鲁胺治疗的患者常见疲劳,腹泻和潮热,其中5(0.6%)名患者出现癫痫发作。恩杂鲁胺是一种非常有效的阻断雄激素信号传导途径的新型疗法,在CRPC的发展过程中不受此调节。将会对临床前研究以及导致其在2012年9月获得美国食品和药物管理局(FDA)批准的关键试验进行审查。

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