首页> 外文期刊>Progres en urologie: journal de l’Association francaise d’urologie et de la Societefrancaise d’urologie >Novel agents for the therapy of castration-resistant prostate cancer: Overview of pivotal studies and new strategies to come [Nouvelles thérapeutiques dans le cancer de la prostate résistant à la castration : Panorama des études pivotales et nouveaux schémas thérapeutiques à venir]
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Novel agents for the therapy of castration-resistant prostate cancer: Overview of pivotal studies and new strategies to come [Nouvelles thérapeutiques dans le cancer de la prostate résistant à la castration : Panorama des études pivotales et nouveaux schémas thérapeutiques à venir]

机译:治疗去势抵抗性前列腺癌的新型药物:关键研究概述和新策略[去势抵抗性前列腺癌的新治疗方法:关键研究和新治疗方案的概述]

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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.
机译:目的:最近,已经开发出用于治疗前列腺癌的新药物。我们的目的是审查涉及去势抵抗性前列腺癌的新型药物治疗的III期研究。方法:在PubMed数据库中搜索以以下搜索词发表的原创文章:前列腺癌,去势抵抗,转移性,靶向治疗,生物制剂,免疫治疗和临床试验。还检索了2008年美国临床肿瘤学会,美国泌尿科协会和欧洲泌尿科协会会议的论文集。我们纳入了涉及以下阶段的III期研究:阿比特龙,MDV 3100,卡巴他赛,西普柳赛尔T,镭223和地诺单抗。结果:在随机试验中,以多西他赛为基础的化疗后,阿比特龙和MDV 3100是两种新的激素疗法,分别显示在多西他赛化疗后的总生存期分别增加了15和18个月。卡巴他赛成为继多西他赛之后的标准二线化疗药物。 Sipuleucel-T已成为前列腺癌中首个获批的疫苗。与安慰剂相比,它的死亡率降低了22%,存活时间延长了4.1个月。在安慰剂对照的随机试验中,基于镭223的代谢放疗已显示出更好的总体生存率,骨骼相关事件的延迟和减少。在唑来膦酸对照试验中,Denosumab还延迟了第一例骨骼相关事件(20.7对17.1个月,P = 0.0002)。此外,与安慰剂相比,地诺单抗将骨转移延迟了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。他们在去势抵抗性前列腺癌的治疗方法中添加了新的工具。

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