Spyropoulos Evangelos, Kotsiris Dimitrios, Spyropoulos Katherine, Panagopoulos Aggelos, Galanakis Ioannis, Mavrikos Stamatios
Urology Department, Naval and Veterans Hospital of Athens, Athens, Greece.
Urology Department, Naval and Veterans Hospital of Athens, Athens, Greece.
Clin Genitourin Cancer. 2017 Feb;15(1):129-138.e1. doi: 10.1016/j.clgc.2016.06.018. Epub 2016 Jun 29.
We developed a mathematical "prostate cancer (PCa) conditions simulating" predictive model (PCP-SMART), from which we derived a novel PCa predictor (prostate cancer risk determinator [PCRD] index) and a PCa risk equation. We used these to estimate the probability of finding PCa on prostate biopsy, on an individual basis.
A total of 371 men who had undergone transrectal ultrasound-guided prostate biopsy were enrolled in the present study. Given that PCa risk relates to the total prostate-specific antigen (tPSA) level, age, prostate volume, free PSA (fPSA), fPSA/tPSA ratio, and PSA density and that tPSA ≥ 50 ng/mL has a 98.5% positive predictive value for a PCa diagnosis, we hypothesized that correlating 2 variables composed of 3 ratios (1, tPSA/age; 2, tPSA/prostate volume; and 3, fPSA/tPSA; 1 variable including the patient's tPSA and the other, a tPSA value of 50 ng/mL) could operate as a PCa conditions imitating/simulating model. Linear regression analysis was used to derive the coefficient of determination (R), termed the PCRD index. To estimate the PCRD index's predictive validity, we used the χ test, multiple logistic regression analysis with PCa risk equation formation, calculation of test performance characteristics, and area under the receiver operating characteristic curve analysis using SPSS, version 22 (P < .05).
The biopsy findings were positive for PCa in 167 patients (45.1%) and negative in 164 (44.2%). The PCRD index was positively signed in 89.82% positive PCa cases and negative in 91.46% negative PCa cases (χ test; P < .001; relative risk, 8.98). The sensitivity was 89.8%, specificity was 91.5%, positive predictive value was 91.5%, negative predictive value was 89.8%, positive likelihood ratio was 10.5, negative likelihood ratio was 0.11, and accuracy was 90.6%. Multiple logistic regression revealed the PCRD index as an independent PCa predictor, and the formulated risk equation was 91% accurate in predicting the probability of finding PCa. On the receiver operating characteristic analysis, the PCRD index (area under the curve, 0.926) significantly (P < .001) outperformed other, established PCa predictors.
The PCRD index effectively predicted the prostate biopsy outcome, correctly identifying 9 of 10 men who were eventually diagnosed with PCa and correctly ruling out PCa for 9 of 10 men who did not have PCa. Its predictive power significantly outperformed established PCa predictors, and the formulated risk equation accurately calculated the probability of finding cancer on biopsy, on an individual patient basis.
我们开发了一种数学“前列腺癌(PCa)病情模拟”预测模型(PCP - SMART),从中得出了一种新型的PCa预测指标(前列腺癌风险测定仪[PCRD]指数)以及一个PCa风险方程。我们利用这些来逐个估计在前列腺活检中发现PCa的概率。
本研究共纳入371例接受经直肠超声引导下前列腺活检的男性患者。鉴于PCa风险与总前列腺特异性抗原(tPSA)水平、年龄、前列腺体积、游离PSA(fPSA)、fPSA/tPSA比值以及PSA密度相关,且tPSA≥50 ng/mL对PCa诊断的阳性预测值为98.5%,我们假设由3个比值组成的2个变量(1. tPSA/年龄;2. tPSA/前列腺体积;3. fPSA/tPSA;1个变量包含患者的tPSA,另一个变量为tPSA值50 ng/mL)可作为一种PCa病情模拟模型。采用线性回归分析得出决定系数(R),即PCRD指数。为评估PCRD指数的预测有效性,我们使用χ检验、构建PCa风险方程的多元逻辑回归分析、计算检验性能特征以及使用SPSS 22版软件进行受试者工作特征曲线下面积分析(P <.05)。
167例患者(45.1%)活检结果为PCa阳性,164例(44.2%)为阴性。PCRD指数在PCa阳性病例中的阳性率为89.82%,在PCa阴性病例中的阴性率为91.46%(χ检验;P <.001;相对风险为8.98)。敏感性为89.8%,特异性为91.5%,阳性预测值为91.5%,阴性预测值为89.8%,阳性似然比为10.5,阴性似然比为0.11,准确性为90.6%。多元逻辑回归显示PCRD指数是独立的PCa预测指标,构建的风险方程在预测发现PCa的概率方面准确率为91%。在受试者工作特征分析中,PCRD指数(曲线下面积为0.926)显著优于其他已有的PCa预测指标(P <.001)。
PCRD指数有效预测了前列腺活检结果,能正确识别出最终被诊断为PCa的10名男性中的9名,也能正确排除10名未患PCa男性中的9名的PCa诊断。其预测能力显著优于已有的PCa预测指标,构建的风险方程能准确计算出个体患者活检时发现癌症的概率。