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去势联合尼鲁米特与去势联合安慰剂治疗晚期前列腺癌:一项综述

Castration plus nilutamide vs castration plus placebo in advanced prostate cancer. A review.

作者信息

Du Plessis D J

机构信息

Department of Urology, University of Pretoria, South Africa.

出版信息

Urology. 1991;37(2 Suppl):20-4. doi: 10.1016/0090-4295(91)80097-q.

Abstract

Combination of antiandrogen treatment with surgical or medical castration should improve the efficacy of endocrine treatment of prostatic cancer by blocking the effects of adrenal androgens. A nonsteroidal antiandrogen, nilutamide, has shown promising results in preliminary open studies. In a short-term (29 days) comparison of nilutamide plus buserelin and buserelin plus placebo, nilutamide (300 mg/day), significantly reduced bone pain, and fewer patients experienced worsening pain than in the control group. The initial buserelin-induced increase in prostatic acid phosphatase was prevented by nilutamide, but there was a similar increase in testosterone and gonadotropin concentrations to that seen in the control group. Thus, nilutamide can prevent the tumor flare-up associated with the start of luteinizing hormone-releasing hormone (LH-RH) treatment, even though the endocrine responses are not affected. In three multicenter, randomized, double-blind placebo-controlled trials of castration and nilutamide involving 248 patients, the combination of nilutamide and castration decreased bone pain, improved performance status, and increased the number of patients with objective regression, compared with patients who were castrated but did not receive nilutamide. Nilutamide was generally well tolerated, though visual disorders, gastrointestinal disorders, and alcohol intolerance were reported in patients receiving nilutamide. The results suggest that nilutamide improves the efficacy of castration in patients with prostatic cancer. Current studies are investigating the effects of this treatment on survival and the risk-benefit ratio.

摘要

抗雄激素治疗与手术或药物去势相结合,应能通过阻断肾上腺雄激素的作用来提高前列腺癌内分泌治疗的疗效。一种非甾体类抗雄激素药物尼鲁米特,在初步的开放性研究中已显示出有前景的结果。在一项尼鲁米特加布舍瑞林与布舍瑞林加安慰剂的短期(29天)比较中,尼鲁米特(300毫克/天)显著减轻了骨痛,且与对照组相比,经历疼痛加重的患者更少。尼鲁米特阻止了最初布舍瑞林引起的前列腺酸性磷酸酶升高,但睾酮和促性腺激素浓度的升高与对照组相似。因此,尼鲁米特可以预防与促黄体生成素释放激素(LH-RH)治疗开始相关的肿瘤 flare-up,尽管内分泌反应未受影响。在三项涉及248名患者的去势与尼鲁米特的多中心、随机、双盲、安慰剂对照试验中,与接受去势但未接受尼鲁米特的患者相比,尼鲁米特与去势的联合治疗减轻了骨痛,改善了身体状况,并增加了客观缓解的患者数量。尼鲁米特总体耐受性良好,不过接受尼鲁米特治疗患者报告有视觉障碍、胃肠道疾病和酒精不耐受情况。结果表明,尼鲁米特可提高前列腺癌患者去势治疗的疗效。目前的研究正在调查这种治疗对生存的影响以及风险效益比。

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