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[去势抵抗性前列腺癌治疗的新型药物:关键研究综述及未来新策略]

[Novel agents for the therapy of castration-resistant prostate cancer: overview of pivotal studies and new strategies to come].

作者信息

Ouzaid I, Ravery V, Pouessel D, Culine S

机构信息

Service d'urologie, université Paris Diderot, hôpital Bichat Claude-Bernard, Assistance Publique-Hôpitaux de Paris, 46, rue Henri-Huchard, 75018 Paris, France.

出版信息

Prog Urol. 2013 Jan;23(1):1-7. doi: 10.1016/j.purol.2012.07.007. Epub 2012 Aug 13.

Abstract

OBJECTIVE

Recently, new agents have been developed in the treatment of prostate cancer. Our aim was to review phase III studies that involved novel agents in the treatment of castration resistant prostate cancer.

METHODS

PubMed databases were searched for original articles published with the search terms: prostate cancer, castration resistant, metastatic, targeted therapy, biologic agents, immunotherapy and clinical trials. Proceedings from 2008 of conferences of the American Society of Clinical Oncology, American Urological Association, and the European Association of Urology were also searched. We included phase III studies that involved: abiraterone, MDV 3100, cabazitaxel, sipuleucel-T, radium-223, and denosumab.

RESULTS

Abiraterone and MDV 3100 are two new hormotherapies that showed an increased overall survival of 15 and 18 months respectively before after docetaxel based chemotherapy in randomized trials. Cabazitaxel became the standard second line chemotherapy after docetaxel. Sipuleucel-T has emerged as the first approved vaccine in prostate cancer. It showed a 22 % reduction of mortality and a prolonged survival time of 4.1 months compared to placebo. A radium-223 based metabolic radiotherapy has showed a better overall survival, delayed and reduced skeletal-related events in placebo controlled randomized trials. Denosumab also delayed the first skeletal-related event in a zoledronic acid controlled trial (20.7 versus 17.1 months, P=0.0002). Moreover, Denosumab delays bone metastases by 4.1 months compared to placebo.

CONCLUSION

The novel agents that emerged in the treatment of prostate cancer showed an efficacy in placebo controlled trials. They added new tools in the armamentarium of therapies of castration resistant prostate cancer.

摘要

目的

最近,已开发出用于治疗前列腺癌的新型药物。我们的目的是回顾涉及新型药物治疗去势抵抗性前列腺癌的III期研究。

方法

在PubMed数据库中搜索发表的原始文章,搜索词为:前列腺癌、去势抵抗性、转移性、靶向治疗、生物制剂、免疫疗法和临床试验。还搜索了2008年美国临床肿瘤学会、美国泌尿外科学会和欧洲泌尿外科学会会议的会议记录。我们纳入了涉及以下药物的III期研究:阿比特龙、MDV 3100、卡巴他赛、西妥昔单抗、镭-223和地诺单抗。

结果

阿比特龙和MDV 3100是两种新的激素疗法,在随机试验中,基于多西他赛的化疗前后,总体生存期分别增加了15个月和18个月。卡巴他赛成为多西他赛后的标准二线化疗药物。西妥昔单抗已成为前列腺癌中首个获批的疫苗。与安慰剂相比,它显示死亡率降低了22%,生存时间延长了4.1个月。在安慰剂对照的随机试验中,基于镭-223的代谢放疗显示出更好的总体生存期、延迟并减少了骨相关事件。在唑来膦酸对照试验中,地诺单抗也延迟了首次骨相关事件的发生(20.7个月对17.1个月,P=0.0002)。此外,与安慰剂相比,地诺单抗使骨转移延迟了4.1个月。

结论

在前列腺癌治疗中出现的新型药物在安慰剂对照试验中显示出疗效。它们为去势抵抗性前列腺癌的治疗增添了新的手段。

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