Abstract:Histological classification of colorectal polyps plays a critical role in both screening for colorectal cancer and care of affected patients. In this study, we developed a deep neural network for classification of four major colorectal polyp types on digitized histopathology slides and compared its performance to local pathologists' diagnoses at the point-of-care retrieved from corresponding pathology labs. We evaluated the deep neural network on an internal dataset of 157 histopathology slides from the Dartmouth-Hitchcock Medical Center (DHMC) in New Hampshire, as well as an external dataset of 513 histopathology slides from 24 different institutions spanning 13 states in the United States. For the internal evaluation, the deep neural network had a mean accuracy of 93.5% (95% CI 89.6%-97.4%), compared with local pathologists' accuracy of 91.4% (95% CI 87.0%-95.8%). On the external test set, the deep neural network achieved an accuracy of 85.7% (95% CI 82.7%-88.7%), significantly outperforming the accuracy of local pathologists at 80.9% (95% CI 77.5%-84.3%, p<0.05) at the point-of-care. If confirmed in clinical settings, our model could assist pathologists by improving the diagnostic efficiency, reproducibility, and accuracy of colorectal cancer screenings.
Abstract:Deep learning for classification of microscopy images is challenging because whole-slide images are high resolution. Due to the large size of these images, they cannot be transferred into GPU memory, so there are currently no end-to-end deep learning architectures for their analysis. Existing work has used a sliding window for crop classification, followed by a heuristic to determine the label for the whole slide. This pipeline is not efficient or robust, however, because crops are analyzed independently of their neighbors and the decisive features for classifying a whole slide are only found in a few regions of interest. In this paper, we present an attention-based model for classification of high resolution microscopy images. Our model dynamically finds regions of interest from a wide-view, then identifies characteristic patterns in those regions for whole-slide classification. This approach is analogous to how pathologists examine slides under the microscope and is the first to generalize the attention mechanism to high resolution images. Furthermore, our model does not require bounding box annotations for the regions of interest and is trainable end-to-end with flexible input. We evaluated our model on a microscopy dataset of Barrett's Esophagus images, and the results showed that our approach outperforms the current state-of-the-art sliding window method by a large margin.