Classification of Prostatic Carcinoma with Artificial Neural Networks Using Comparative Genomic Hybridization and Quantitative Stereological Data

• Published in: Pathology, research and practice Vol. 199; no. 12; pp. 773 - 784
• Main Authors: Mattfeldt, Torsten, Gottfried, Hans-Werner, Wolter, Hubertus, Schmidt, Volker, Kestler, Hans A., Mayer, Johannes
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.01.2003; Elsevier Science Ltd
• Subjects: Adenocarcinoma - classification; Adenocarcinoma - genetics; Adenocarcinoma - pathology; Artificial neural networks; Chromosome Aberrations; Comparative genomic hybridization; DNA, Neoplasm - analysis; Humans; Image Processing, Computer-Assisted; Imaging, Three-Dimensional; Male; Neoplasm Staging; Neural Networks (Computer); Nucleic Acid Hybridization; Pattern recognition; Prostate cancer; Prostatic Neoplasms - classification; Prostatic Neoplasms - genetics; Prostatic Neoplasms - pathology; Reproducibility of Results; Stereology; Stereology; Pattern recognition; Comparative genomic hybridization; Prostate cancer; Artificial neural networks
• ISSN: 0344-0338; 1618-0631
• DOI: 10.1078/0344-0338-00496

Staging of prostate cancer is a mainstay of treatment decisions and prognostication. In the present study, 50 pT2N0 and 28 pT3N0 prostatic adenocarcinomas were characterized by Gleason grading, comparative genomic hybridization (CGH), and histological texture analysis based on principles of stereology and stochastic geometry. The cases were classified by learning vector quantization and support vector machines. The quality of classification was tested by cross-validation. Correct prediction of stage from primary tumor data was possible with an accuracy of 74– 80% from different data sets. The accuracy of prediction was similar when the Gleason score was used as input variable, when stereological data were used, or when a combination of CGH data and stereological data was used. The results of classification by learning vector quantization were slightly better than those by support vector machines. A method is briefly sketched by which training of neural networks can be adapted to unequal sample sizes per class. Progression from pT2 to pT3 prostate cancer is correlated with complex changes of the epithelial cells in terms of volume fraction, of surface area, and of second-order stereological properties. Genetically, this progression is accompanied by a significant global increase in losses and gains of DNA, and specifically by increased numerical aberrations on chromosome arms 1q, 7p, and 8p.