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去势抵抗性前列腺癌的治疗选择:当前疗法及基于多西他赛的新兴方案

Treatment options in castration-resistant prostate cancer: current therapies and emerging docetaxel-based regimens.

作者信息

Saad Fred, Miller Kurt

机构信息

University of Montreal Hospital Center, Montreal, Quebec, Canada.

Department of Urology, Charité Berlin, Berlin, Germany.

出版信息

Urol Oncol. 2014 Feb;32(2):70-9. doi: 10.1016/j.urolonc.2013.01.005. Epub 2013 Mar 15.

Abstract

BACKGROUND

Docetaxel-based chemotherapy remains the standard of care for metastatic castration-resistant prostate cancer (mCRPC) and it is the only globally approved first-line therapy. Although docetaxel offers improved survival for this patient population, it is also associated with toxicity and resistance in many patients, representing a need for more efficacious therapies. Preclinical advances have led to improved understanding of the molecular biology of prostate cancer, and targeted therapies that exploit the signaling pathways and molecular targets that underscore the disease are being clinically investigated in combination with docetaxel.

DESIGN

This article briefly highlights recent data from phase III trials in mCRPC that have led to agent approval. This article also reviews phase II and III trials in which docetaxel-based regimens have been investigated in mCRPC.

RESULTS

Recently approved agents, including sipuleucel-T, cabazitaxel, abiraterone acetate, and enzalutamide, have diversified the mCRPC treatment landscape. Phase III trials evaluating docetaxel in combination with targeted therapies, including potent oral tyrosine kinase inhibitor, dasatinib, in the READY trial and clusterin inhibitor, custirsen, in the SYNERGY trial, are currently ongoing.

CONCLUSIONS

In combination with docetaxel, targeted agents dasatinib and custirsen will likely expand the existing treatment paradigm for mCRPC if results from phase III trials are positive.

摘要

背景

基于多西他赛的化疗仍然是转移性去势抵抗性前列腺癌(mCRPC)的标准治疗方法,且是唯一全球获批的一线治疗方案。尽管多西他赛可提高该患者群体的生存率,但在许多患者中也会引发毒性和耐药性问题,这表明需要更有效的治疗方法。临床前研究的进展加深了对前列腺癌分子生物学的理解,目前正在对与多西他赛联合使用的、针对该疾病所强调的信号通路和分子靶点的靶向治疗进行临床研究。

设计

本文简要介绍了mCRPC III期试验中已促成药物获批的最新数据。本文还回顾了在mCRPC中对基于多西他赛的治疗方案进行研究的II期和III期试验。

结果

最近获批的药物,包括sipuleucel-T、卡巴他赛、醋酸阿比特龙和恩杂鲁胺,使mCRPC的治疗格局更加多样化。目前正在进行III期试验,评估多西他赛与靶向治疗联合使用的效果,包括在READY试验中使用强效口服酪氨酸激酶抑制剂达沙替尼,以及在SYNERGY试验中使用簇集素抑制剂库司替丁。

结论

如果III期试验结果呈阳性,那么靶向药物达沙替尼和库司替丁与多西他赛联合使用可能会扩大mCRPC现有的治疗模式。

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