A new artificial intelligence system successfully detects and localises early neoplasia in Barrett's esophagus by using convolutional neural networks.

AI Barrett's Esophagus CAD CNN artificial intelligence computer aided detection convolutional neural networks early detection early neoplasia neoplasia

Journal

United European gastroenterology journal
ISSN: 2050-6414
Titre abrégé: United European Gastroenterol J
Pays: England
ID NLM: 101606807

Informations de publication

Date de publication:
07 2022
Historique:
received: 05 12 2021
accepted: 31 03 2022
pubmed: 7 5 2022
medline: 16 7 2022
entrez: 6 5 2022
Statut: ppublish

Résumé

Seattle protocol biopsies for Barrett's Esophagus (BE) surveillance are labour intensive with low compliance. Dysplasia detection rates vary, leading to missed lesions. This can potentially be offset with computer aided detection. We have developed convolutional neural networks (CNNs) to identify areas of dysplasia and where to target biopsy. 119 Videos were collected in high-definition white light and optical chromoendoscopy with i-scan (Pentax Hoya, Japan) imaging in patients with dysplastic and non-dysplastic BE (NDBE). We trained an indirectly supervised CNN to classify images as dysplastic/non-dysplastic using whole video annotations to minimise selection bias and maximise accuracy. The CNN was trained using 148,936 video frames (31 dysplastic patients, 31 NDBE, two normal esophagus), validated on 25,161 images from 11 patient videos and tested on 264 iscan-1 images from 28 dysplastic and 16 NDBE patients which included expert delineations. To localise targeted biopsies/delineations, a second directly supervised CNN was generated based on expert delineations of 94 dysplastic images from 30 patients. This was tested on 86 i-scan one images from 28 dysplastic patients. The indirectly supervised CNN achieved a per image sensitivity in the test set of 91%, specificity 79%, area under receiver operator curve of 93% to detect dysplasia. Per-lesion sensitivity was 100%. Mean assessment speed was 48 frames per second (fps). 97% of targeted biopsy predictions matched expert and histological assessment at 56 fps. The artificial intelligence system performed better than six endoscopists. Our CNNs classify and localise dysplastic Barrett's Esophagus potentially supporting endoscopists during surveillance.

Sections du résumé

BACKGROUND AND AIMS
Seattle protocol biopsies for Barrett's Esophagus (BE) surveillance are labour intensive with low compliance. Dysplasia detection rates vary, leading to missed lesions. This can potentially be offset with computer aided detection. We have developed convolutional neural networks (CNNs) to identify areas of dysplasia and where to target biopsy.
METHODS
119 Videos were collected in high-definition white light and optical chromoendoscopy with i-scan (Pentax Hoya, Japan) imaging in patients with dysplastic and non-dysplastic BE (NDBE). We trained an indirectly supervised CNN to classify images as dysplastic/non-dysplastic using whole video annotations to minimise selection bias and maximise accuracy. The CNN was trained using 148,936 video frames (31 dysplastic patients, 31 NDBE, two normal esophagus), validated on 25,161 images from 11 patient videos and tested on 264 iscan-1 images from 28 dysplastic and 16 NDBE patients which included expert delineations. To localise targeted biopsies/delineations, a second directly supervised CNN was generated based on expert delineations of 94 dysplastic images from 30 patients. This was tested on 86 i-scan one images from 28 dysplastic patients.
FINDINGS
The indirectly supervised CNN achieved a per image sensitivity in the test set of 91%, specificity 79%, area under receiver operator curve of 93% to detect dysplasia. Per-lesion sensitivity was 100%. Mean assessment speed was 48 frames per second (fps). 97% of targeted biopsy predictions matched expert and histological assessment at 56 fps. The artificial intelligence system performed better than six endoscopists.
INTERPRETATION
Our CNNs classify and localise dysplastic Barrett's Esophagus potentially supporting endoscopists during surveillance.

Identifiants

pubmed: 35521666
doi: 10.1002/ueg2.12233
pmc: PMC9278593
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

528-537

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 203145Z/16/Z
Pays : United Kingdom
Organisme : Cancer Research UK
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.

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Auteurs

Mohamed Hussein (M)

Division of Surgery and Interventional Sciences, University College London, London, UK.
Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.
Department of Gastroenterology, University College London Hospital, London, UK.

Juana González-Bueno Puyal (J)

Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.
Odin Vision, London, UK.

David Lines (D)

Odin Vision, London, UK.

Vinay Sehgal (V)

Department of Gastroenterology, University College London Hospital, London, UK.

Daniel Toth (D)

Odin Vision, London, UK.

Omer F Ahmad (OF)

Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.
Department of Gastroenterology, University College London Hospital, London, UK.

Rawen Kader (R)

Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.

Martin Everson (M)

Division of Surgery and Interventional Sciences, University College London, London, UK.

Gideon Lipman (G)

Division of Surgery and Interventional Sciences, University College London, London, UK.

Jacobo Ortiz Fernandez-Sordo (JO)

NIHR Nottingham Digestive Diseases Biomedical Research Centre, Nottingham, UK.

Krish Ragunath (K)

NIHR Nottingham Digestive Diseases Biomedical Research Centre, Nottingham, UK.

Jose Miguel Esteban (JM)

Clínico San Carlos, Madrid, Spain.

Matthew Banks (M)

Department of Gastroenterology, University College London Hospital, London, UK.

Michael Haefner (M)

St Elisabeth Hospital, Vienna, Austria.

Peter Mountney (P)

Odin Vision, London, UK.

Danail Stoyanov (D)

Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.

Laurence B Lovat (LB)

Division of Surgery and Interventional Sciences, University College London, London, UK.
Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.
Department of Gastroenterology, University College London Hospital, London, UK.

Rehan Haidry (R)

Division of Surgery and Interventional Sciences, University College London, London, UK.
Wellcome/EPSRC Centre for Interventional and Surgical Sciences (WEISS), University College London, London, UK.
Department of Gastroenterology, University College London Hospital, London, UK.

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