External validation of an artificial neural network and two nomograms for prostate cancer detection.

ISRN urology Pub Date : 2012-01-01 Epub Date: 2012-07-05 DOI:10.5402/2012/643181
Thorsten H Ecke, Steffen Hallmann, Stefan Koch, Jürgen Ruttloff, Henning Cammann, Holger Gerullis, Kurt Miller, Carsten Stephan
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Abstract

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.

Abstract Image

Abstract Image

用于前列腺癌检测的人工神经网络和两个提名图的外部验证。
背景。多变量模型用于提高前列腺癌(PCa)的检出率,减少不必要的活检。我们利用日常数据对人工神经网络(ANN)"ProstataClass"(ANN-Charité)进行了外部验证。材料和方法。人工神经网络的单项预测是利用人工神经网络应用软件生成的,用于检测 PSA 和游离 PSA,其依据是年龄、tPSA、%fPSA、前列腺体积和 DRE (ANN-Charité)。通过 ROC 曲线分析以及观察概率与预测概率的比较,对 tPSA、%fPSA 和 ANN 的诊断有效性进行了评估。结果显示共检测出 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,提名图I为0.713,提名图II为0.742,与%fPSA相比,提名图II具有显著优势(P = 0.009),而其他模型与%fPSA没有差异(P = 0.15和P = 0.41)。所有模型都高估了预测的 PCa 概率。结论。除 ROC 分析外,校准也是确定临床实践中使用模型真实价值的重要工具。如果在不了解模型开发情况的情况下进行外部验证,多变量模型的价值就会受到限制。
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