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目前和新兴的治疗方法在去势抵抗性前列腺癌的管理。

Current and emerging treatments in the management of castration-resistant prostate cancer.

机构信息

Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

Expert Rev Anticancer Ther. 2012 Jul;12(7):951-64. doi: 10.1586/era.12.59.

Abstract

Historically, patients diagnosed with castration-resistant prostate cancer (CRPC) have had poor survival rates. In recent years there have been significant advances in the treatment of CRPC. In addition to cytotoxic chemotherapy, treating physicians and their patients now have the option of several new agents that target not only androgen- and cytotoxic-mediated pathways, but also the patient's own immune system. In this review, we discuss the existing US FDA-approved therapies, a wide range of experimental treatments that are currently in development, and also palliative options for patients with symptoms secondary to metastatic disease. We also discuss the progression-free survival, overall survival, PSA levels and other end points used in clinical trials in order to evaluate and compare novel therapeutic options for CRPC. Currently, docetaxel and sipuleucel-T are the first line treatment options for patients with CRPC; approved second-line treatments for first line treatment failure are limited to cabazitaxel and abiraterone acetate. Recently, a few experimental agents, MDV3100 and radium-223, have demonstrated efficacy in improving overall survival in patients who had previously failed chemotherapy. These agents, and possibly others introduced in this review, are positioned to change the treatment landscape for CRPC.

摘要

从历史上看,被诊断患有去势抵抗性前列腺癌(CRPC)的患者生存率一直较差。近年来,CRPC 的治疗取得了重大进展。除细胞毒性化疗外,治疗医生及其患者现在还可以选择几种新的药物,这些药物不仅针对雄激素和细胞毒性介导的途径,而且还针对患者自身的免疫系统。在这篇综述中,我们讨论了现有的美国食品和药物管理局 (FDA) 批准的疗法、目前正在开发的广泛的实验性治疗方法,以及针对转移性疾病引起的症状的姑息治疗选择。我们还讨论了用于评估和比较 CRPC 新型治疗选择的临床试验中的无进展生存期、总生存期、PSA 水平和其他终点。目前,多西他赛和 sipuleucel-T 是 CRPC 患者的一线治疗选择;对于一线治疗失败的批准二线治疗方法仅限于卡巴他赛和阿比特龙醋酸酯。最近,一些实验性药物,如 MDV3100 和镭-223,已证明在改善先前化疗失败的患者的总生存期方面有效。这些药物以及本文中介绍的其他药物有望改变 CRPC 的治疗格局。

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