Computer-aided prediction of polyp histology on white light colonoscopy using surface pattern analysis.


Journal

Endoscopy
ISSN: 1438-8812
Titre abrégé: Endoscopy
Pays: Germany
ID NLM: 0215166

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 26 10 2018
medline: 21 4 2020
entrez: 26 10 2018
Statut: ppublish

Résumé

This study aimed to evaluate a new computational histology prediction system based on colorectal polyp textural surface patterns using high definition white light images. Textural elements (textons) were characterized according to their contrast with respect to the surface, shape, and number of bifurcations, assuming that dysplastic polyps are associated with highly contrasted, large tubular patterns with some degree of bifurcation. Computer-aided diagnosis (CAD) was compared with pathological diagnosis and the diagnosis made by endoscopists using Kudo and Narrow-Band Imaging International Colorectal Endoscopic classifications. Images of 225 polyps were evaluated (142 dysplastic and 83 nondysplastic). The CAD system correctly classified 205 polyps (91.1 %): 131/142 dysplastic (92.3 %) and 74/83 (89.2 %) nondysplastic. For the subgroup of 100 diminutive polyps (≤ 5 mm), CAD correctly classified 87 polyps (87.0 %): 43/50 (86.0 %) dysplastic and 44/50 (88.0 %) nondysplastic. There were no statistically significant differences in polyp histology prediction between the CAD system and endoscopist assessment. A computer vision system based on the characterization of the polyp surface in white light accurately predicted colorectal polyp histology.

Sections du résumé

BACKGROUND
This study aimed to evaluate a new computational histology prediction system based on colorectal polyp textural surface patterns using high definition white light images.
METHODS
Textural elements (textons) were characterized according to their contrast with respect to the surface, shape, and number of bifurcations, assuming that dysplastic polyps are associated with highly contrasted, large tubular patterns with some degree of bifurcation. Computer-aided diagnosis (CAD) was compared with pathological diagnosis and the diagnosis made by endoscopists using Kudo and Narrow-Band Imaging International Colorectal Endoscopic classifications.
RESULTS
Images of 225 polyps were evaluated (142 dysplastic and 83 nondysplastic). The CAD system correctly classified 205 polyps (91.1 %): 131/142 dysplastic (92.3 %) and 74/83 (89.2 %) nondysplastic. For the subgroup of 100 diminutive polyps (≤ 5 mm), CAD correctly classified 87 polyps (87.0 %): 43/50 (86.0 %) dysplastic and 44/50 (88.0 %) nondysplastic. There were no statistically significant differences in polyp histology prediction between the CAD system and endoscopist assessment.
CONCLUSION
A computer vision system based on the characterization of the polyp surface in white light accurately predicted colorectal polyp histology.

Identifiants

pubmed: 30360010
doi: 10.1055/a-0732-5250
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

261-265

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Georg Thieme Verlag KG Stuttgart · New York.

Déclaration de conflit d'intérêts

María Pellisé has been consultant for Norgine Iberia from 2012 to 2017. She has received speaker fees from Norgine Iberia, Casen Recordati and Olympus Spain in the last 5 years. Gloria Fernández-Esparrach has received fees for organizing courses from Norgine Iberia and Olympus Spain in the last two years and has been consultant for a trial design for CDx Diagnostics

Auteurs

Cristina Sánchez-Montes (C)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

Francisco Javier Sánchez (FJ)

Computer Science Department, Universitat Autònoma de Barcelona and Computer Vision Center, Barcelona, Spain.

Jorge Bernal (J)

Computer Science Department, Universitat Autònoma de Barcelona and Computer Vision Center, Barcelona, Spain.

Henry Córdova (H)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

María López-Cerón (M)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

Miriam Cuatrecasas (M)

Pathology Department, Centre de Diagnòstic Biomèdic, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.
Banc de Tumors-Biobanc Clínic, IDIBAPS-XBTC, Barcelona, Spain.

Cristina Rodríguez de Miguel (C)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

Ana García-Rodríguez (A)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

Rodrigo Garcés-Durán (R)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

María Pellisé (M)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

Josep Llach (J)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

Glòria Fernández-Esparrach (G)

Endoscopy Unit, Gastroenterology Department, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Spain.

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Classifications MeSH