Prediction of early colorectal cancer metastasis by machine learning using digital slide images.


Journal

Computer methods and programs in biomedicine
ISSN: 1872-7565
Titre abrégé: Comput Methods Programs Biomed
Pays: Ireland
ID NLM: 8506513

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 10 02 2019
revised: 08 06 2019
accepted: 21 06 2019
entrez: 17 8 2019
pubmed: 17 8 2019
medline: 23 2 2020
Statut: ppublish

Résumé

Prediction of lymph node metastasis (LNM) for early colorectal cancer (CRC) is critical for determining treatment strategies after endoscopic resection. Some histologic parameters for predicting LNM have been established, but evaluator error and inter-observer disagreement are unsolved issues. Here we describe an LNM prediction algorithm for submucosal invasive (T1) CRC based on machine learning. We conducted a retrospective single-institution study of 397 T1 CRCs. Several morphologic parameters were extracted from whole slide images of cytokeratin immunohistochemistry using Image J. A random forest algorithm for a training dataset (n = 277) was executed and used to predict LNM for the test dataset (n = 120). The results were compared with conventional histologic evaluation of hematoxylin-eosin staining. Machine learning showed better LNM predictive ability than the conventional method on some datasets. Cross validation revealed no significant difference between the methods. Machine learning resulted in fewer false-negative cases than the conventional method. Machine learning on whole slide images is a potential alternative for determining treatment strategies for T1 CRC.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
Prediction of lymph node metastasis (LNM) for early colorectal cancer (CRC) is critical for determining treatment strategies after endoscopic resection. Some histologic parameters for predicting LNM have been established, but evaluator error and inter-observer disagreement are unsolved issues. Here we describe an LNM prediction algorithm for submucosal invasive (T1) CRC based on machine learning.
METHODS METHODS
We conducted a retrospective single-institution study of 397 T1 CRCs. Several morphologic parameters were extracted from whole slide images of cytokeratin immunohistochemistry using Image J. A random forest algorithm for a training dataset (n = 277) was executed and used to predict LNM for the test dataset (n = 120). The results were compared with conventional histologic evaluation of hematoxylin-eosin staining.
RESULTS RESULTS
Machine learning showed better LNM predictive ability than the conventional method on some datasets. Cross validation revealed no significant difference between the methods. Machine learning resulted in fewer false-negative cases than the conventional method.
CONCLUSIONS CONCLUSIONS
Machine learning on whole slide images is a potential alternative for determining treatment strategies for T1 CRC.

Identifiants

pubmed: 31416544
pii: S0169-2607(19)30197-X
doi: 10.1016/j.cmpb.2019.06.022
pii:
doi:

Substances chimiques

Keratins 68238-35-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-161

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Manabu Takamatsu (M)

Division of Pathology, The Cancer Institute; Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan. Electronic address: manabu.takamatsu@jfcr.or.jp.

Noriko Yamamoto (N)

Division of Pathology, The Cancer Institute; Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Hiroshi Kawachi (H)

Division of Pathology, The Cancer Institute; Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Akiko Chino (A)

Department of Endoscopy, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Shoichi Saito (S)

Department of Endoscopy, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Masashi Ueno (M)

Department of Colorectal Surgery, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yuichi Ishikawa (Y)

Division of Pathology, The Cancer Institute; Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Yutaka Takazawa (Y)

Division of Pathology, The Cancer Institute; Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

Kengo Takeuchi (K)

Division of Pathology, The Cancer Institute; Department of Pathology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

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