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Enzalutamide for treatment of CRPC: Rationale for sequencing and potential clinical biomarker for resistance

机译:恩扎鲁胺治疗CRPC:测序的依据和耐药性的潜在临床生物标志物

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摘要

The androgen receptor (AR) is central to the initiation and progression of prostate cancer, even after castration. There has been some success in therapies targeting AR signaling which have been shown to extend survival in men with castration-resistant prostate cancer (CRPC). Enzalutamide is a potent AR antagonist that was initially approved in 2012 for men with CRPC who had previously failed chemotherapy treatment with docetaxel. Herein, we reviewed 2 key manuscripts that have recently appeared in the New England Journal of Medicine regarding enzalutamide. The PREVAIL Phase 3 trial was designed to evaluate enzalutamide before chemotherapy in men with CRPC. The study illustrated that 65% of patients receiving enzalutamide had radiographic-progression free survival. There was a significant risk reduction of radiographic progression or death, compared with the placebo group. The enzalutamide group's median overall survival was 32.4 months vs. 30.2 months in the placebo group.
机译:雄激素受体(AR)即使在去势后也对前列腺癌的发生和发展至关重要。在靶向AR信号转导的疗法中已经取得了一些成功,已证明可以延长男性去势抵抗性前列腺癌(CRPC)的生存期。 Enzalutamide是一种有效的AR拮抗剂,最初于2012年被批准用于先前用多西他赛化疗失败的CRPC男性。在这里,我们回顾了最近在《新英格兰医学杂志》上发表的有关enzalutamide的2篇主要手稿。 PREVAIL 3期试验旨在评估男性CRPC化疗前的恩杂鲁胺。研究表明,接受恩杂鲁胺治疗的患者中有65%的患者无影像学进展。与安慰剂组相比,显着降低了放射学进展或死亡的风险。恩杂鲁胺组的中位总生存期为32.4个月,而安慰剂组为30.2个月。

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