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雄激素剥夺及晚期前列腺癌的其他治疗方法。

Androgen deprivation and other treatments for advanced prostate cancer.

作者信息

Brawer M K, Crawford E D, Labrie F, Mendoza-Valdes A, Miller P D, Petrylak D P

出版信息

Rev Urol. 2001;3 Suppl 2(Suppl 2):S59-68.

Abstract

Among the issues discussed at this year's meeting on prostate cancer in Vail, Colorado, were several that specifically relate to the patient with advanced disease. Dr. E. David Crawford addressed the issue of the timing of hormone therapy, specifically reviewing several important trials that give a glimpse at the potential outcome of aggressive treatment in stage D1.5. The efficacy of antiandrogens, flutamide, bicalutamide, and nilutamide, when combined with chemical or surgical castration, was reviewed. Dr. Arturo Mendoza-Valdes reviewed the rationale behind intermittent (versus continuous) total androgen blockade, especially as related to quality of life. Dr. Paul Miller gave an update on the role of bisphosphonates as adjuvant therapy for prostate cancer. Also discussed was an important new agent for androgen deprivation, Abarelix, a sustained-release GnRH antagonist with low histamine-releasing potential which avoids testosterone and other hormone surge and flare.

摘要

在今年于科罗拉多州韦尔举行的前列腺癌会议上讨论的诸多问题中,有几个特别涉及晚期疾病患者。E. 大卫·克劳福德博士探讨了激素治疗的时机问题,具体回顾了几项重要试验,这些试验让我们得以一窥D1.5期积极治疗的潜在结果。还回顾了抗雄激素药物氟他胺、比卡鲁胺和尼鲁米特与药物或手术去势联合使用时的疗效。阿图罗·门多萨 - 巴尔德斯博士阐述了间歇性(与持续性相对)全雄激素阻断背后的原理,尤其是与生活质量相关的方面。保罗·米勒博士介绍了双膦酸盐作为前列腺癌辅助治疗的作用的最新情况。还讨论了一种重要的雄激素剥夺新药阿巴瑞克,它是一种缓释GnRH拮抗剂,组胺释放潜力低,可避免睾酮及其他激素的激增和波动。

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