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Toward Interpretable Cell Image Representation and Abnormality Scoring for Cervical Cancer Screening Using Pap Smears.
Ando, Yu; Cho, Junghwan; Park, Nora Jee-Young; Ko, Seokhwan; Han, Hyungsoo.
Affiliation
  • Ando Y; Department of Biomedical Science, Kyungpook National University, Daegu 41566, Republic of Korea.
  • Cho J; Clinical Omics Institute, Kyungpook National University, Daegu 41405, Republic of Korea.
  • Park NJ; Department of Pathology, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea.
  • Ko S; Department of Pathology, Kyunpook National University Chilgok Hospital, Daegu 41404, Republic of Korea.
  • Han H; Department of Biomedical Science, Kyungpook National University, Daegu 41566, Republic of Korea.
Bioengineering (Basel) ; 11(6)2024 Jun 04.
Article de En | MEDLINE | ID: mdl-38927803
ABSTRACT
Screening is critical for prevention and early detection of cervical cancer but it is time-consuming and laborious. Supervised deep convolutional neural networks have been developed to automate pap smear screening and the results are promising. However, the interest in using only normal samples to train deep neural networks has increased owing to the class imbalance problems and high-labeling costs that are both prevalent in healthcare. In this study, we introduce a method to learn explainable deep cervical cell representations for pap smear cytology images based on one-class classification using variational autoencoders. Findings demonstrate that a score can be calculated for cell abnormality without training models with abnormal samples, and we localize abnormality to interpret our results with a novel metric based on absolute difference in cross-entropy in agglomerative clustering. The best model that discriminates squamous cell carcinoma (SCC) from normals gives 0.908±0.003 area under operating characteristic curve (AUC) and one that discriminates high-grade epithelial lesion (HSIL) 0.920±0.002 AUC. Compared to other clustering methods, our method enhances the V-measure and yields higher homogeneity scores, which more effectively isolate different abnormality regions, aiding in the interpretation of our results. Evaluation using an external dataset shows that our model can discriminate abnormality without the need for additional training of deep models.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Bioengineering (Basel) Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Bioengineering (Basel) Année: 2024 Type de document: Article