Internal validation of an artificial neural network for prostate biopsy outcome

被引:8
作者
Stephan, Carsten [1 ]
Cammann, Henning [2 ]
Bender, Martin
Miller, Kurt
Lein, Michael [3 ]
Jung, Klaus [3 ]
Meyer, Hellmuth-A
机构
[1] Charite, Dept Urol, CCM, D-10117 Berlin, Germany
[2] Charite, Inst Med Informat, D-10117 Berlin, Germany
[3] Berlin Inst Urol Res, Berlin, Germany
关键词
artificial neural network; multivariate models; prostate cancer; prostate-specific antigen; validation; REGRESSION-BASED NOMOGRAMS; CANCER DETECTION; ANTIGEN; SERUM; MODELS; PSA; POPULATIONS; PREDICTION; JAPANESE; NG/ML;
D O I
10.1111/j.1442-2042.2009.02417.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To carry out an internal validation of the retrospectively trained artificial neural network (ANN) 'ProstataClass'. Methods: A prospectively collected database of 393 patients undergoing 8-12 core prostate biopsy was analyzed. Data of these patients were applied to the online available ANN 'ProstataClass' using the Elecsys total prostate-specific antigen (tPSA) and free PSA (fPSA) assays. Beside the internal validation of the ANN 'ProstataClass' an additional ANN (named as ANN internal validation: ANNiv) only using the 393 prospective patient data was evaluated. The new ANN model was constructed with the MATLAB Neural Network Toolbox. Diagnostic accuracy was evaluated by receiver operator characteristic (ROC) curves comparing the areas under the ROC curves (AUC) and specificities at 90% and 95% sensitivity. Results: Within a tPSA range of 1.0-22.8 ng/mL, 229 men (58.3%) had prostate cancer (PCa). tPSA, %fPSA and the number of positive digital rectal examinations (DRE) differed significantly from the cohort of patients of the ANN 'ProstataClass', whereas age and prostate volume were comparable. AUCs for tPSA, %fPSA and the ANN 'ProstataClass' were 0.527, 0.726 and 0.747 (P = 0.085 between %fPSA and ANN). The AUC of the ANNiv (0.754) was significantly better compared with %fPSA (P = 0.021), whereas the AUC of two ANN models built on external cohorts (0.726 and 0.729) showed no differences to %fPSA and the other ANN models. Conclusions: Significant differences of DRE status and %fPSA medians decrease the power of the 'ProstataClass' ANN in the internal validation cohort. The effect of retrospective data evaluation the 'ProstataClass' cohort and prospective fPSA measurement may be responsible for %fPSA differences. All ANN models built with different PSA and fPSA assays performed equally if applied to the two cohorts.
引用
收藏
页码:62 / 68
页数:7
相关论文
共 22 条
  • [1] Use of the percentage of free prostate-specific antigen to enhance differentiation of prostate cancer from benign prostatic disease - A prospective multicenter clinical trial
    Catalona, WJ
    Partin, AW
    Slawin, KM
    Brawer, MK
    Flanigan, RC
    Patel, A
    Richie, JP
    deKernion, JB
    Walsh, PC
    Scardino, PT
    Lange, PH
    Subong, ENP
    Parson, RE
    Gasior, GH
    Loveland, KG
    Southwick, PC
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (19): : 1542 - 1547
  • [2] Initial biopsy outcome prediction - Head-to-head comparison of a logistic regression-based nomogram versus artificial neural network
    Chun, Felix K. -H.
    Graefen, Markus
    Briganti, Alberto
    Gallina, Andrea
    Hopp, Julia
    Kattan, Michael W.
    Huland, Hartwig
    Karakiewicz, Pierre I.
    [J]. EUROPEAN UROLOGY, 2007, 51 (05) : 1236 - 1243
  • [3] A critical appraisal of logistic regression-based nomograms, artificial neural networks, classification and regression-tree models, look-up tables and risk-group stratification models for prostate cancer
    Chun, Felix K. -H.
    Karakiewicz, Pierre I.
    Briganti, Alberto
    Walz, Jochen
    Kattan, Michael W.
    Huland, Hartwig
    Graefen, Markus
    [J]. BJU INTERNATIONAL, 2007, 99 (04) : 794 - 800
  • [4] Predicting the outcome of prostate biopsy in screen-positive men by a multilayer perceptron network
    Finne, P
    Finne, R
    Auvinen, A
    Juusela, H
    Aro, J
    Määttänen, L
    Hakama, M
    Rannikko, S
    Tammela, TLJ
    Stenman, UH
    [J]. UROLOGY, 2000, 56 (03) : 418 - 422
  • [5] SOFTWARE FOR ILLUSTRATIVE PRESENTATION OF BASIC CLINICAL CHARACTERISTICS OF LABORATORY TESTS - GRAPHROC FOR WINDOWS
    KAIRISTO, V
    POOLA, A
    [J]. SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1995, 55 : 43 - 60
  • [6] A neurocomputational model for prostate carcinoma detection
    Kalra, P
    Togami, J
    Bansal, G
    Partin, AW
    Brawer, MK
    Babaian, RJ
    Ross, LS
    Niederberger, CS
    [J]. CANCER, 2003, 98 (09) : 1849 - 1854
  • [7] Development and validation of a nomogram predicting the outcome of prostate biopsy based on patient age, digital rectal examination and serum prostate specific antigen
    Karakiewicz, PI
    Benayoun, S
    Kattan, MW
    Perrotte, P
    Valiquette, L
    Scardino, PT
    Cagiannos, I
    Heinzer, H
    Tanguay, S
    Aprikian, AG
    Huland, H
    Graefen, M
    [J]. JOURNAL OF UROLOGY, 2005, 173 (06) : 1930 - 1934
  • [8] Development, validation, and head-to-head comparison of logistic regression-based nomograms and artificial neural network models predicting prostate cancer on initial extended biopsy
    Kawakami, Satoru
    Numao, Noboru
    Okubo, Yuhei
    Koga, Fumitaka
    Yamamoto, Shinya
    Saito, Kazutaka
    Fujii, Yasuhisa
    Yonese, Junji
    Masuda, Hitoshi
    Kihara, Kazunori
    Fukui, Iwao
    [J]. EUROPEAN UROLOGY, 2008, 54 (03) : 601 - 611
  • [9] Development of a new nomogram for predicting the probability of a positive initial prostate biopsy in Japanese patients with serum PSA levels less than 10 ng/mL
    Kawamura, Koji
    Suzuki, Hiroyoshi
    Kamiya, Naoto
    Imamoto, Takashi
    Yano, Masashi
    Miura, Junichiro
    Shimbo, Masaki
    Suzuki, Noriyuki
    Nakatsu, Hiroomi
    Ichikawa, Tomohiko
    [J]. INTERNATIONAL JOURNAL OF UROLOGY, 2008, 15 (07) : 598 - 603
  • [10] Prostate-specific antigen and prostate cancer: prediction, detection and monitoring
    Lilja, Hans
    Ulmert, David
    Vickers, Andrew J.
    [J]. NATURE REVIEWS CANCER, 2008, 8 (04) : 268 - 278