Gan Gao, Renao Yan, Andrew H Song, Huai-Ching Hsieh, Lindsey A Erion Barner, Fiona Wang, David Brenes, Sarah S L Chow, Rui Wang, Kevin W Bishop, Yongjun Liu, Xavier Farre, Mukul Divatia, Michelle R Downes, Funda Vakar-Lopez, Priti Lal, Wynn Burke, Anant Madabhushi, Lawrence D True, Deepti M Reddi, William M Grady, Faisal Mahmood, Jonathan T C Liu
Standard slide-based two-dimensional (2D) histopathology severely undersamples spatially heterogeneous tissue, with each thin 2D section representing <1% of the entire biopsy volume. Recent advances in non-destructive three-dimensional (3D) pathology, such as open-top light-sheet microscopy, enable comprehensive high-resolution imaging of large clinical specimens. Since manual review of these massive and complex 3D datasets is infeasible in clinical practice, we present TRICARE, a deep-learning triage framework that identifies high-risk 2D cross sections within 3D pathology datasets to enable time-efficient pathologist evaluation, which offers a lower-risk route for accelerated adoption by retaining pathologists for final diagnoses. TRICARE assigns risk scores to all 2D levels within a tissue volume by leveraging context from a subset of neighbouring depth levels, outperforming models in which predictions are based on isolated 2D levels. In two use cases-risk stratification based on prostate cancer biopsies and screening for dysplasia/cancer in endoscopic biopsies of Barrett's esophagus-AI-triaged 3D pathology, enabled by TRICARE, demonstrates the potential to improve the detection of high-risk diseases compared with slide-based 2D histopathology while optimizing pathologist workloads.