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Nilutamide: possible utility as a second-line hormonal agent.

机译:尼鲁米特:可能作为二线激素药物。

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OBJECTIVES: To study the ability of nilutamide to induce prostate-specific antigen (PSA) responses in patients with hormone-resistant prostate cancer who had been exposed to prior antiandrogen therapy, because resistance to antiandrogens may be mediated by altered binding to a mutated or overexpressed androgen receptor and because an alternative antiandrogen may overcome such resistance. Nilutamide is a little used antiandrogen that has a chemical structure distinct from that of the other two antiandrogens, flutamide and bicalutamide. METHODS: Fourteen patients with hormone-resistant prostate cancer were treated with nilutamide 150 mg/day (n = 12) or 300 mg/day (n = 2). Seven had been treated with one prior antiandrogen (all with bicalutamide), five with both bicalutamide and flutamide, and two had received bicalutamide and prior chemotherapy. RESULTS: In a retrospective analysis, 7 (50%) of the 14 patients had a greater than 50% decline in their PSA level, and 4 of the 6 patients with bone pain experienced subjective improvement. The median duration of the PSA response was 11 months (range 2 to 28+) with 2 of the 7 patients still experiencing a PSA response. In addition, 3 patients (20%) had brief and minor PSA responses (less than 50%). CONCLUSIONS: A subset of patients, whose disease progresses with prior antiandrogen therapy, may experience a PSA response to nilutamide. The role of nilutamide in such hormone-resistant patients deserves additional prospective study.
机译:目的:研究尼鲁米特在先前接受过抗雄激素治疗的激素抵抗性前列腺癌患者中诱导前列腺特异性抗原(PSA)反应的能力,因为对抗雄激素的抗性可能是由于与突变或过表达的结合改变而介导的雄激素受体,因为替代的抗雄激素可以克服这种耐药性。尼鲁米特是一种很少使用的抗雄激素,其化学结构不同于其他两种抗雄激素氟他胺和比卡鲁胺。方法:14名激素抵抗性前列腺癌患者接受尼鲁米特150毫克/天(n = 12)或300毫克/天(n = 2)治疗。七名曾接受过一种抗雄激素治疗(全部接受了比卡鲁胺治疗),五名同时接受了比卡鲁胺和氟他胺治疗,另外两人接受了比卡鲁胺和先前的化疗。结果:在一项回顾性分析中,14名患者中有7名(50%)的PSA下降幅度大于50%,而6名骨痛患者中有4名主观改善。 PSA反应的中位持续时间为11个月(范围2至28+),而7例患者中仍有2例仍经历PSA反应。此外,有3例患者(20%)发生了短暂和轻微的PSA反应(少于50%)。结论:一部分患者在先前的抗雄激素治疗下病情发展,可能会发生对尼鲁胺的PSA反应。尼鲁米特在这类激素抵抗性患者中的作用值得进一步的前瞻性研究。

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