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Ensemble Deep Learning Model to Predict Lymphovascular Invasion in Gastric Canceropen access

Authors
Lee, JonghyunCha, SeunghyunKim, JiwonKim, Jung JooKim, NamkugJae Gal, Seong GyuKim, Ju HanLee, Jeong HoonChoi, Yoo-DukKang, Sae-RyungSong, Ga-YoungYang, Deok-HwanLee, Jae-HyukLee, Kyung-HwaAhn, SangjeongMoon, Kyoung MinNoh, Myung-Giun
Issue Date
Jan-2024
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
digital pathology; artificial intelligence; gastric cancer; lymphovascular invasion
Citation
Cancers, v.16, no.2
Indexed
SCIE
SCOPUS
Journal Title
Cancers
Volume
16
Number
2
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/65450
DOI
10.3390/cancers16020430
ISSN
2072-6694
Abstract
Simple Summary Lymphovascular invasion (LVI) serves as a crucial predictor in gastric cancer, indicating an increased likelihood of lymph node spread and poorer patient outcomes. Detecting LVI(+) within gastric cancer histopathology presents challenges due to its elusive nature, leading to the proposal of a deep learning-based detection method using H&E-stained whole-slide images. Remarkably, both the classification and detection models demonstrated superior performance, and their ensemble exhibited outstanding predictive capabilities in identifying LVI areas. This innovative approach holds promise in precision medicine, potentially streamlining examinations and reducing discrepancies among pathologists.Abstract Lymphovascular invasion (LVI) is one of the most important prognostic factors in gastric cancer as it indicates a higher likelihood of lymph node metastasis and poorer overall outcome for the patient. Despite its importance, the detection of LVI(+) in histopathology specimens of gastric cancer can be a challenging task for pathologists as invasion can be subtle and difficult to discern. Herein, we propose a deep learning-based LVI(+) detection method using H&E-stained whole-slide images. The ConViT model showed the best performance in terms of both AUROC and AURPC among the classification models (AUROC: 0.9796; AUPRC: 0.9648). The AUROC and AUPRC of YOLOX computed based on the augmented patch-level confidence score were slightly lower (AUROC: -0.0094; AUPRC: -0.0225) than those of the ConViT classification model. With weighted averaging of the patch-level confidence scores, the ensemble model exhibited the best AUROC, AUPRC, and F1 scores of 0.9880, 0.9769, and 0.9280, respectively. The proposed model is expected to contribute to precision medicine by potentially saving examination-related time and labor and reducing disagreements among pathologists.
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Ahn, Sang Jeong
Anam Hospital (Department of Pathology, Anam Hospital)
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