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Prognostic significance of the nadir prostate specific antigen level after hormone therapy for prostate cancer.

机译:激素治疗后最低谷前列腺特异性抗原水平对前列腺癌的预后意义。

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PURPOSE: We determine whether the nadir prostate specific antigen (PSA) level after hormone therapy can be used to predict the progression to hormone refractory prostate cancer. MATERIALS AND METHODS: We reviewed the progressive status and survival of 177 patients with stage C or D prostate cancer who had received hormone therapy at our institution. The overall survival rate, incidence of progression to hormone refractory prostate cancer and interval until progression were analyzed with reference to the nadir PSA level. Multiple regression analysis was used to analyze the predictive factors for progression to hormone refractory prostate cancer, and the relative efficacy of the nadir PSA level in predicting progression was evaluated by receiver operating characteristics analysis. RESULTS: Median followup was 39 months (range 3 to 89) and 85.4% of patients (151) responded to treatment, of whom 77.5% (117) had progression to hormone refractory prostate cancer. Median time until nadir PSA levels were reached after hormone therapy was 8.1 months and median time until hormone refractory prostate cancer was 24.0 months. Nadir PSA levels were less than 0.2 ng./ml. in 31% of respondents, 0.2 to 1.0 ng./ml. in 23%, 1.1 to 10 ng./ml. in 42% and greater than 10 ng./ml. in 5%. These groups had similar clinicopathological characteristics. Nadir PSA levels correlated significantly with pretreatment PSA levels, Gleason scores and progression to hormone refractory prostate cancer (p = 0.01, p <0.01 and p <0.001, respectively), and inversely correlated with the interval to the establishment of hormone refractory prostate cancer (r = -0.465, p <0.05). By univariate analysis bone metastasis, nadir PSA, PSA at 6 months after treatment and pretreatment PSA were significantly associated with progression to hormone refractory prostate cancer. Only the nadir PSA was calculated to be an independent factor by multivariate analysis. Receiver operating characteristics analysis indicated that nadir PSA predicted progression to hormone refractory prostate cancer after 2 years with an accuracy of 86.2%. With the lower limit of the nadir PSA level set to 1.1 ng./ml., sensitivity was 80.3% and specificity was 83.8%, and these levels were deemed the most appropriate. Furthermore, nadir PSA after hormone therapy was an independent prognosticator for survival, as were initial levels of hemoglobin and alkaline phosphatase. CONCLUSIONS: The nadir PSA level after hormone therapy may be the most accurate factor predicting the progression to hormone refractory prostate cancer and is an independent prognostic factor for survival. Furthermore, a lower limit for the nadir PSA level of 1.1 ng./ml. gives optimal sensitivity and specificity.
机译:目的:我们确定激素治疗后的最低前列腺特异性抗原(PSA)水平是否可用于预测激素难治性前列腺癌的进展。材料与方法:我们回顾了在我们机构接受激素治疗的177例C期或D期前列腺癌患者的进展状况和生存情况。参照最低PSA水平分析了总生存率,激素难治性前列腺癌进展的发生率以及直至进展的间隔。使用多元回归分析来分析激素难治性前列腺癌进展的预测因素,并通过接受者操作特征分析评估最低点PSA水平在预测进展中的相对功效。结果:中位随访时间为39个月(范围3至89),有85.4%的患者(151)对治疗有反应,其中77.5%(117)的患者进展为激素难治性前列腺癌。激素治疗后直至达到最低PSA水平的中位时间为8.1个月,直到激素难治性前列腺癌的中位时间为24.0个月。最低PSA水平低于0.2 ng./ml。在31%的受访者中,浓度为0.2至1.0 ng./ml。含量为23%,1.1至10 ng./ml。含量为42%且大于10 ng./ml。在5%。这些组具有相似的临床病理特征。 Nadir PSA水平与治疗前PSA水平,Gleason评分和进展为激素难治性前列腺癌显着相关(分别为p = 0.01,p <0.01和p <0.001),并且与激素难治性前列腺癌发生的时间间隔呈负相关( r = -0.465,p <0.05)。通过单因素分析,骨转移,最低点PSA,治疗前和治疗前6个月的PSA与激素难治性前列腺癌的进展显着相关。通过多变量分析,仅最低点PSA被计算为独立因素。接受者操作特征分析表明,最低点PSA预测2年后会发展为激素难治性前列腺癌,准确率达86.2%。将最低PSA水平的下限设置为1.1 ng./ml时,敏感性为80.3%,特异性为83.8%,这些水平被认为是最合适的。此外,激素治疗后最低点PSA以及存活率是血红蛋白和碱性磷酸酶初始水平的独立预后指标。结论:激素治疗后的最低PSA水平可能是预测激素难治性前列腺癌进展的最准确因素,并且是生存的独立预后因素。此外,最低PSA水平的下限为1.1 ng./ml。提供最佳的敏感性和特异性。

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