Ecke Thorsten H, Hallmann Steffen, Koch Stefan, Ruttloff Jürgen, Cammann Henning, Gerullis Holger, Miller Kurt, Stephan Carsten
Department of Urology, HELIOS Hospital, 15526 Bad Saarow, Germany.
ISRN Urol. 2012;2012:643181. doi: 10.5402/2012/643181. Epub 2012 Jul 5.
Background. Multivariate models are used to increase prostate cancer (PCa) detection rate and to reduce unnecessary biopsies. An external validation of the artificial neural network (ANN) "ProstataClass" (ANN-Charité) was performed with daily routine data. Materials and Methods. The individual ANN predictions were generated with the use of the ANN application for PSA and free PSA assays, which rely on age, tPSA, %fPSA, prostate volume, and DRE (ANN-Charité). Diagnostic validity of tPSA, %fPSA, and the ANN was evaluated by ROC curve analysis and comparisons of observed versus predicted probabilities. Results. Overall, 101 (35.8%) PCa were detected. The areas under the ROC curve (AUCs) were 0.501 for tPSA, 0.669 for %fPSA, 0.694 for ANN-Charité, 0.713 for nomogram I, and 0.742 for nomogram II, showing a significant advantage for nomogram II (P = 0.009) compared with %fPSA while the other model did not differ from %fPSA (P = 0.15 and P = 0.41). All models overestimated the predicted PCa probability. Conclusions. Beside ROC analysis, calibration is an important tool to determine the true value of using a model in clinical practice. The worth of multivariate models is limited when external validations were performed without knowledge of the circumstances of the model's development.
背景。多变量模型用于提高前列腺癌(PCa)的检出率并减少不必要的活检。使用日常常规数据对人工神经网络(ANN)“ProstataClass”(ANN-Charité)进行了外部验证。材料与方法。使用依赖于年龄、总前列腺特异抗原(tPSA)、游离前列腺特异抗原百分比(%fPSA)、前列腺体积和直肠指检(DRE)的ANN应用程序生成个体ANN预测结果(ANN-Charité)。通过ROC曲线分析以及观察概率与预测概率的比较来评估tPSA、%fPSA和ANN的诊断有效性。结果。总体而言,共检测出101例(35.8%)PCa。tPSA的ROC曲线下面积(AUC)为0.501,%fPSA为0.669,ANN-Charité为0.694,列线图I为0.713,列线图II为0.742,与%fPSA相比,列线图II显示出显著优势(P = 0.009),而其他模型与%fPSA无差异(P = 0.15和P = 0.41)。所有模型均高估了预测的PCa概率。结论。除了ROC分析外,校准是确定在临床实践中使用模型的真实价值的重要工具。在不了解模型开发情况的前提下进行外部验证时,多变量模型的价值有限。