首页> 外文期刊>Urology >ProPSA and diagnostic biopsy tissue DNA content combination improves accuracy to predict need for prostate cancer treatment among men enrolled in an active surveillance program.
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ProPSA and diagnostic biopsy tissue DNA content combination improves accuracy to predict need for prostate cancer treatment among men enrolled in an active surveillance program.

机译:ProPSA和诊断性活检组织DNA含量的组合提高了准确性,从而可以预测参加主动监测计划的男性中需要进行前列腺癌治疗的人数。

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OBJECTIVES: To assess a novel application of the Prostate Health Index (phi) and biopsy tissue DNA content in benign-adjacent and cancer areas to predict which patients would eventually require treatment of prostate cancer in the Proactive Surveillance cohort. METHODS: We identified 71 men who had had serum and biopsy tissue from their diagnosis banked and available for the present study. Of the 71 patients, 39 had developed unfavorable biopsy findings and 32 had maintained favorable biopsy status during surveillance. The serum total prostate-specific antigen (tPSA), free PSA (fPSA) and [-2]proPSA were measured using the Beckman Coulter immunoassay. The DNA content measurements of Feulgen-stained biopsy sections were performed using the AutoCyte imaging system. RESULTS: The ratio of phi was significantly greater (37.23 +/- 15.76 vs 30.60 +/- 12.28; P = .03) in men who ultimately had unfavorable biopsy findings. The serum phi ratio (P = .003), [-2]proPSA/%fPSA (P = .004), biopsy tissue DNA content (ie, benign-adjacent excess of optical density, P = .019; and cancer area standard deviation of optical density, P = .002) were significant predictors of unfavorable biopsy conversion on Cox regression analysis. However, phi and [-2]proPSA/%fPSA showed a highly significant correlation (rho = 0.927, P < .0001) and no difference in accuracy (c-index, 0.6247 vs 0.6158; P = .704) for unfavorable biopsy conversion prediction. Furthermore, phi and [-2]proPSA/%fPSA remained significant (P = .047 and P = .036, respectively) in the multivariate models and, combined with the biopsy tissue DNA content, showed improvement in the predictive accuracy (c-index, 0.6908 and 0.6884, respectively) for unfavorable biopsy conversion. CONCLUSIONS: The Prostate Health Index to proPSA/%fPSA, combined with biopsy tissue DNA content, improved the accuracy to about 70% to predict unfavorable biopsy conversion at the annual surveillance biopsy examination among men enrolled in an Active Surveillance program.
机译:目的:评估前列腺健康指数(phi)和活检组织DNA含量在良性毗邻和癌症地区的新应用,以预测哪些患者最终将在主动监测队列中需要治疗前列腺癌。方法:我们从他们的诊断中确定了71名具有血清和活检组织的男性,这些男性可以用于本研究。在71例患者中,有39例活检发现不良,在监测期间有32例维持良好的活检状态。使用贝克曼库尔特免疫测定法测量血清总前列腺特异性抗原(tPSA),游离PSA(fPSA)和[-2] proPSA。使用AutoCyte成像系统对Feulgen染色的活检切片的DNA含量进行测量。结果:在最终发现活检结果不利的男性中,phi的比率明显更高(37.23 +/- 15.76与30.60 +/- 12.28; P = .03)。血清phi比(P = .003),[-2] proPSA /%fPSA(P = .004),活检组织DNA含量(即,光密度的良性和邻接性过高,P = .019;和癌区标准) Cox回归分析显示,光密度的偏差(P = 0.002)是活检转换不良的重要预测指标。但是,对于不利的活检转换,phi和[-2] proPSA /%fPSA显示出高度显着的相关性(rho = 0.927,P <.0001),准确性无差异(c指数,0.6247 vs 0.6158; P = .704)。预测。此外,在多变量模型中,phi和[-2] proPSA /%fPSA仍然显着(分别为P = .047和P = .036),并与活检组织DNA含量结合显示出预测准确性的改善(c-不利的活检转换)(分别为0.6908和0.6884)。结论:proPSA /%fPSA的前列腺健康指数与活检组织DNA含量相结合,可将参加主动监测计划的男性的年度监测活检检查的准确性提高到约70%,以预测活检转换的不利情况。

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