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首页> 外文期刊>Urology >Prostate-specific antigen doubling time predicts response to deferred antiandrogen therapy in men with androgen-independent prostate cancer.
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Prostate-specific antigen doubling time predicts response to deferred antiandrogen therapy in men with androgen-independent prostate cancer.

机译:前列腺特异性抗原加倍时间预测患有雄激素非依赖性前列腺癌的男性对延缓抗雄激素治疗的反应。

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摘要

OBJECTIVES: To identify the pretreatment variables that are predictive of response and the duration of response to deferred antiandrogen therapy in men with androgen-independent prostate cancer (AIPC). METHODS: A total of 375 patients receiving androgen deprivation therapy for advanced prostate cancer between 1977 and 2002 had medical records available for retrospective review. Of these 375 patients, 163 were diagnosed with AIPC. The inclusion criteria included (1) diagnosis of AIPC and (2) treatment with deferred antiandrogen therapy. AIPC was biochemically defined as two consecutive rises in the prostate-specific antigen (PSA) level during androgen deprivation therapy. The treatment response to deferred antiandrogen therapy was defined as a 50% or greater decline in the pretreatment PSA level. The prognostic value of various pretreatment parameters was determined with the appropriate statistical methods and tested with a Cox proportional hazards model. RESULTS: Of the 163 patients with AIPC, 36 were treated with deferred antiandrogen therapy. Of these 36 patients, 12 (33.3%) experienced a PSA response. The median PSA failure-free survival was 9.0 months (95% confidence interval 5.2 to 12.9). The only pretreatment variable predictive of a PSA response was the PSA doubling time (PSADT). The mean PSADT in responders was 12.7 months versus 7.5 months in nonresponders (P = 0.037). Moreover, PSADT was the only statistically significant variable on univariate analysis of PSA failure-free survival in responders (hazard ratio 0.202, 95% confidence interval 0.041 to 0.990, P = 0.049). No statistically significant difference was found in cancer-specific survival between responders and nonresponders (P = 0.1501). CONCLUSIONS: The PSADT predicted both the response and the duration of the response to deferred antiandrogen therapy in patients diagnosed with AIPC.
机译:目的:确定可预测雄激素非依赖性前列腺癌(AIPC)男性对延缓抗雄激素治疗的反应和反应持续时间的预处理变量。方法:1977年至2002年间,共375例接受了雄激素剥夺治疗的晚期前列腺癌患者的病历可供回顾。在这375名患者中,有163名被诊断出患有AIPC。纳入标准包括(1)AIPC的诊断和(2)延缓抗雄激素疗法的治疗。 AIPC被生化定义为雄激素剥夺治疗期间前列腺特异性抗原(PSA)水平连续两次升高。延缓抗雄激素治疗的治疗反应定义为治疗前PSA水平下降50%或更大。使用适当的统计方法确定各种预处理参数的预后价值,并使用Cox比例风险模型进行测试。结果:163例AIPC患者中,有36例接受了延迟抗雄激素治疗。在这36名患者中,有12名(33.3%)经历了PSA反应。 PSA无故障生存的中位数为9.0个月(95%置信区间5.2至12.9)。预测PSA反应的唯一预处理变量是PSA倍增时间(PSADT)。应答者的平均PSADT为12.7个月,而非应答者为7.5个月(P = 0.037)。此外,在单因素分析中,PSADT是响应者PSA无故障生存的唯一统计上显着变量(危险比0.202,95%置信区间0.041至0.990,P = 0.049)。在应答者和非应答者之间,在癌症特异性存活率上没有发现统计学上的显着差异(P = 0.1501)。结论:PSADT预测了延迟诊断的抗雄激素治疗对AIPC患者的反应和反应持续时间。

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