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Deep Learning-Based Screening of Urothelial Carcinoma in Whole Slide Images of Liquid-Based Cytology Urine Specimens

SIMPLE SUMMARY: In this study, we aimed to investigate the use of deep learning for classifying whole-slide images of urine liquid-based cytology specimens into neoplastic and non-neoplastic (negative). To do so, we used a total of 786 whole-slide images to train models using four different approach...

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Detalles Bibliográficos
Autores principales: Tsuneki, Masayuki, Abe, Makoto, Kanavati, Fahdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818219/
https://www.ncbi.nlm.nih.gov/pubmed/36612222
http://dx.doi.org/10.3390/cancers15010226
Descripción
Sumario:SIMPLE SUMMARY: In this study, we aimed to investigate the use of deep learning for classifying whole-slide images of urine liquid-based cytology specimens into neoplastic and non-neoplastic (negative). To do so, we used a total of 786 whole-slide images to train models using four different approaches, and we evaluated them on 750 whole-slide images. The best model achieved good classification performance, demonstrating the promising potential of use of such models for aiding the screening process for urothelial carcinoma in routine clinical practices. ABSTRACT: Urinary cytology is a useful, essential diagnostic method in routine urological clinical practice. Liquid-based cytology (LBC) for urothelial carcinoma screening is commonly used in the routine clinical cytodiagnosis because of its high cellular yields. Since conventional screening processes by cytoscreeners and cytopathologists using microscopes is limited in terms of human resources, it is important to integrate new deep learning methods that can automatically and rapidly diagnose a large amount of specimens without delay. The goal of this study was to investigate the use of deep learning models for the classification of urine LBC whole-slide images (WSIs) into neoplastic and non-neoplastic (negative). We trained deep learning models using 786 WSIs by transfer learning, fully supervised, and weakly supervised learning approaches. We evaluated the trained models on two test sets, one of which was representative of the clinical distribution of neoplastic cases, with a combined total of 750 WSIs, achieving an area under the curve for diagnosis in the range of 0.984–0.990 by the best model, demonstrating the promising potential use of our model for aiding urine cytodiagnostic processes.