4.8 Article

Deep Learning-Based Classification of Hepatocellular Nodular Lesions on Whole-Slide Histopathologic Images

Journal

GASTROENTEROLOGY
Volume 162, Issue 7, Pages 1948-+

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2022.02.025

Keywords

Artificial Intelligence; Liver Nodules; Hematoxylin-Eosin-Stained Slides; Pathological Diagnosis

Funding

  1. National Natural Science Foundation of China [82073397]
  2. Guangdong Basic and Applied Basic Research Foundation [2019A1515011455]
  3. Natural Science Foundation of Guangdong Province [2018A030313650]
  4. Guangzhou Municipal Science and Technology Project [202102010156, 202102010267]
  5. Natural Science Foundation of China cultivating grant of The Third Affiliated Hospital, Sun Yat-sen University [2020GZRPYMS01, 2021GZRPYQN12]
  6. Guangdong Provincial Key Laboratory of Digestive Cancer Research [2021B1212040006]

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This study developed a deep learning diagnostic model for hepatocellular nodular lesions which improved the histopathologic diagnosis of these lesions, particularly for early hepatocellular carcinoma and risk stratification of patients. The model showed significant advantages in patch-level recognition, especially for fragmentary or scarce biopsy specimens.
BACKGROUND & AIMS: Hepatocellular nodular lesions (HNLs) constitute a heterogeneous group of disorders. Differential diagnosis among these lesions, especially high-grade dysplastic nodules (HGDNs) and well-differentiated hepatocellular carcinoma (WD-HCC), can be challenging, let alone biopsy specimens. We aimed to develop a deep learning system to solve these puzzles, improving the histopathologic diagnosis of HNLs (WD-HCC, HGDN, low-grade DN, focal nodular hyperplasia, hepatocellular adenoma), and background tissues (nodular cirrhosis, normal liver tissue). METHODS: The samples consisting of surgical and biopsy specimens were collected from 6 hospitals. Each specimen was reviewed by 2 to 3 subspecialists. Four deep neural networks (ResNet50, InceptionV3, Xception, and the Ensemble) were used. Their performances were evaluated by confusion matrix, receiver operating characteristic curve, classification map, and heat map. The predictive efficiency of the optimal model was further verified by comparing with that of 9 pathologists. RESULTS: We obtained 213,280 patches from 1115 whole-slide images of 738 patients. An optimal model was finally chosen based on F1 score and area under the curve value, named hepatocellular-nodular artificial intelligence model (HnAIM), with the overall 7-category area under the curve of 0.935 in the independent external validation cohort. For biopsy specimens, the agreement rate with subspecialists' majority opinion was higher for HnAIM than 9 pathologists on both patch level and whole-slide images level. CONCLUSIONS: We first developed a deep learning diagnostic model for HNLs, which performed well and contributed to enhancing the diagnosis rate of early HCC and risk stratification of patients with HNLs. Furthermore, HnAIM had significant advantages in patch-level recognition, with important diagnostic implications for fragmentary or scarce biopsy specimens.

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