Deep learning quantification of percent steatosis in donor liver biopsy frozen sections
Lulu Sun,
Jon N. Marsh,
Matthew K. Matlock,
Ling Chen,
Joseph P. Gaut,
Elizabeth M. Brunt,
S. Joshua Swamidass,
Ta-Chiang Liu
Affiliations
Lulu Sun
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States
Jon N. Marsh
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States; Institue for Informatics (I2), Washington University School of Medicine, St. Louis, MO, United States
Matthew K. Matlock
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States
Ling Chen
Division of Biostatistics, Washington University School of Medicine, St. Louis, MO, United States
Joseph P. Gaut
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States
Elizabeth M. Brunt
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States
S. Joshua Swamidass
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States; Institue for Informatics (I2), Washington University School of Medicine, St. Louis, MO, United States; Corresponding authors: Ta-Chiang Liu (lead contact) and S. Joshua Swamidass, Department of Pathology and Immunology, 660 S. Euclid Ave, Box 8118, Saint Louis, MO, 63110.
Ta-Chiang Liu
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States; Lead contact; Corresponding authors: Ta-Chiang Liu (lead contact) and S. Joshua Swamidass, Department of Pathology and Immunology, 660 S. Euclid Ave, Box 8118, Saint Louis, MO, 63110.
Background: Pathologist evaluation of donor liver biopsies provides information for accepting or discarding potential donor livers. Due to the urgent nature of the decision process, this is regularly performed using frozen sectioning at the time of biopsy. The percent steatosis in a donor liver biopsy correlates with transplant outcome, however there is significant inter- and intra-observer variability in quantifying steatosis, compounded by frozen section artifact. We hypothesized that a deep learning model could identify and quantify steatosis in donor liver biopsies. Methods: We developed a deep learning convolutional neural network that generates a steatosis probability map from an input whole slide image (WSI) of a hematoxylin and eosin-stained frozen section, and subsequently calculates the percent steatosis. Ninety-six WSI of frozen donor liver sections from our transplant pathology service were annotated for steatosis and used to train (n = 30 WSI) and test (n = 66 WSI) the deep learning model. Findings: The model had good correlation and agreement with the annotation in both the training set (r of 0.88, intraclass correlation coefficient [ICC] of 0.88) and novel input test sets (r = 0.85 and ICC=0.85). These measurements were superior to the estimates of the on-service pathologist at the time of initial evaluation (r = 0.52 and ICC=0.52 for the training set, and r = 0.74 and ICC=0.72 for the test set). Interpretation: Use of this deep learning algorithm could be incorporated into routine pathology workflows for fast, accurate, and reproducible donor liver evaluation. Funding: Mid-America Transplant Society