Abstract:Whole Slide Images (WSIs) in digital pathology are used to diagnose cancer subtypes. The difference in procedures to acquire WSIs at various trial sites gives rise to variability in the histopathology images, thus making consistent diagnosis challenging. These differences may stem from variability in image acquisition through multi-vendor scanners, variable acquisition parameters, and differences in staining procedure; as well, patient demographics may bias the glass slide batches before image acquisition. The… Show more
“… 23 , 60 Learning tissue representation is a major step toward closing this gap. 21 , 47 Additionally, employing multimodal domain data, such as pathology reports, can help deep learning attach “context” to its otherwise black-box behaviors when it comes to hierarchical tissue representation in their connectionist topologies. 15 , 26 Fig.…”
“… 23 , 60 Learning tissue representation is a major step toward closing this gap. 21 , 47 Additionally, employing multimodal domain data, such as pathology reports, can help deep learning attach “context” to its otherwise black-box behaviors when it comes to hierarchical tissue representation in their connectionist topologies. 15 , 26 Fig.…”
Out-of-distribution (OOD) generalization, especially for medical setups, is a key challenge in modern machine learning which has only recently received much attention. We investigate how different convolutional pre-trained models perform on OOD test data—that is data from domains that have not been seen during training—on histopathology repositories attributed to different trial sites. Different trial site repositories, pre-trained models, and image transformations are examined as specific aspects of pre-trained models. A comparison is also performed among models trained entirely from scratch (i.e., without pre-training) and models already pre-trained. The OOD performance of pre-trained models on natural images, i.e., (1) vanilla pre-trained ImageNet, (2) semi-supervised learning (SSL), and (3) semi-weakly-supervised learning (SWSL) models pre-trained on IG-1B-Targeted are examined in this study. In addition, the performance of a histopathology model (i.e., KimiaNet) trained on the most comprehensive histopathology dataset, i.e., TCGA, has also been studied. Although the performance of SSL and SWSL pre-trained models are conducive to better OOD performance in comparison to the vanilla ImageNet pre-trained model, the histopathology pre-trained model is still the best in overall. In terms of top-1 accuracy, we demonstrate that diversifying the images in the training using reasonable image transformations is effective to avoid learning shortcuts when the distribution shift is significant. In addition, XAI techniques—which aim to achieve high-quality human-understandable explanations of AI decisions—are leveraged for further investigations.
Investigation of histopathology slides by pathologists is an indispensable component of the routine diagnosis of cancer. Artificial intelligence (AI) has the potential to enhance diagnostic accuracy, improve efficiency, and patient outcomes in clinical pathology. However, variations in tissue preparation, staining protocols, and histopathology slide digitization could result in over-fitting of deep learning models when trained on the data from only one center, thereby underscoring the necessity to generalize deep learning networks for multi-center use. Several techniques, including the use of grayscale images, color normalization techniques, and Adversarial Domain Adaptation (ADA) have been suggested to generalize deep learning algorithms, but there are limitations to their effectiveness and discriminability. Convolutional Neural Networks (CNNs) exhibit higher sensitivity to variations in the amplitude spectrum, whereas humans predominantly rely on phase-related components for object recognition. As such, we propose Adversarial fourIer-based Domain Adaptation (AIDA) which applies the advantages of a Fourier transform in adversarial domain adaptation. We conducted a comprehensive examination of subtype classification tasks in four cancers, incorporating cases from multiple medical centers. Specifically, the datasets included multi-center data for 1113 ovarian cancer cases, 247 pleural cancer cases, 422 bladder cancer cases, and 482 breast cancer cases. Our proposed approach significantly improved performance, achieving superior classification results in the target domain, surpassing the baseline, color augmentation and normalization techniques, and ADA. Furthermore, extensive pathologist reviews suggested that our proposed approach, AIDA, successfully identifies known histotype-specific features. This superior performance highlights AIDA’s potential in addressing generalization challenges in deep learning models for multi-center histopathology datasets.
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