Stephan Carsten, Xu Chuanliang, Finne Patrik, Cammann Henning, Meyer Hellmuth-Alexander, Lein Michael, Jung Klaus, Stenman Ulf-Hakan
Department of Urology, Charité-Universitätsmedizin Berlin, Campus Charité Mitte, Berlin, Germany.
Urology. 2007 Sep;70(3):596-601. doi: 10.1016/j.urology.2007.04.004. Epub 2007 Aug 3.
Different artificial neural networks (ANNs) using total prostate-specific antigen (PSA) and percentage of free PSA (%fPSA) have been introduced to enhance the specificity of prostate cancer detection. The applicability of independently trained ANN and logistic regression (LR) models to different populations regarding the composition (screening versus referred) and different PSA assays has not yet been tested.
Two ANN and LR models using PSA (range 4 to 10 ng/mL), %fPSA, prostate volume, digital rectal examination findings, and patient age were tested. A multilayer perceptron network (MLP) was trained on 656 screening participants (Prostatus PSA assay) and another ANN (Immulite-based ANN [iANN]) was constructed on 606 multicentric urologically referred men. These and other assay-adapted ANN models, including one new iANN-based ANN, were used.
The areas under the curve for the iANN (0.736) and MLP (0.745) were equal but showed no differences to %fPSA (0.725) in the Finnish group. Only the new iANN-based ANN reached a significant larger area under the curve (0.77). At 95% sensitivity, the specificities of MLP (33%) and the new iANN-based ANN (34%) were significantly better than the iANN (23%) and %fPSA (19%). Reverse methodology using the MLP model on the referred patients revealed, in contrast, a significant improvement in the areas under the curve for iANN and MLP (each 0.83) compared with %fPSA (0.70). At 90% and 95% sensitivity, the specificities of all LR and ANN models were significantly greater than those for %fPSA.
The ANNs based on different PSA assays and populations were mostly comparable, but the clearly different patient composition also allowed with assay adaptation no unbiased ANN application to the other cohort. Thus, the use of ANNs in other populations than originally built is possible, but has limitations.
已引入使用总前列腺特异性抗原(PSA)和游离PSA百分比(%fPSA)的不同人工神经网络(ANN),以提高前列腺癌检测的特异性。独立训练的ANN和逻辑回归(LR)模型在不同人群(筛查与转诊)和不同PSA检测方法中的适用性尚未得到检验。
测试了两个使用PSA(范围为4至10 ng/mL)、%fPSA、前列腺体积、直肠指检结果和患者年龄的ANN和LR模型。一个多层感知器网络(MLP)在656名筛查参与者(Prostatus PSA检测方法)上进行训练,另一个ANN(基于免疫比浊法的ANN [iANN])在606名多中心泌尿外科转诊男性中构建。使用了这些以及其他针对检测方法调整的ANN模型,包括一个新的基于iANN的ANN。
在芬兰人群中,iANN(0.736)和MLP(0.745)的曲线下面积相等,但与%fPSA(0.725)相比无差异。只有新的基于iANN的ANN达到了显著更大的曲线下面积(0.77)。在95%灵敏度下,MLP(33%)和新的基于iANN的ANN(34%)的特异性显著优于iANN(23%)和%fPSA(19%)。相比之下,在转诊患者中使用MLP模型的反向方法显示,iANN和MLP的曲线下面积(均为0.83)与%fPSA(0.70)相比有显著改善。在90%和95%灵敏度下,所有LR和ANN模型的特异性均显著高于%fPSA。
基于不同PSA检测方法和人群的ANN大多具有可比性,但明显不同的患者构成也使得即使进行检测方法调整,也无法将ANN无偏地应用于另一队列。因此,在与最初构建时不同的其他人群中使用ANN是可能的,但存在局限性。