Stain-Invariant Representation for Tissue Classification in Histology Images

The process of digitising histology slides involves multiple factors that can affect a whole slide image's (WSI) final appearance, including the staining protocol, scanner, and tissue type. This variability constitutes a domain shift and results in significant problems when training and testing deep learning (DL) algorithms in multi-cohort settings. As such, developing robust and generalisable DL models in computational pathology (CPath) remains an open challenge. In this regard, we propose a framework that generates stain-augmented versions of the training images using stain matrix perturbation. Thereafter, we employed a stain regularisation loss to enforce consistency between the feature representations of the source and augmented images. Doing so encourages the model to learn stain-invariant and, consequently, domain-invariant feature representations. We evaluate the performance of the proposed model on cross-domain multi-class tissue type classification of colorectal cancer images and have achieved improved performance compared to other state-of-the-art methods.

Domain Generalization in Computational Pathology: Survey and Guidelines

Deep learning models have exhibited exceptional effectiveness in Computational Pathology (CPath) by tackling intricate tasks across an array of histology image analysis applications. Nevertheless, the presence of out-of-distribution data (stemming from a multitude of sources such as disparate imaging devices and diverse tissue preparation methods) can cause \emph{domain shift} (DS). DS decreases the generalization of trained models to unseen datasets with slightly different data distributions, prompting the need for innovative \emph{domain generalization} (DG) solutions. Recognizing the potential of DG methods to significantly influence diagnostic and prognostic models in cancer studies and clinical practice, we present this survey along with guidelines on achieving DG in CPath. We rigorously define various DS types, systematically review and categorize existing DG approaches and resources in CPath, and provide insights into their advantages, limitations, and applicability. We also conduct thorough benchmarking experiments with 28 cutting-edge DG algorithms to address a complex DG problem. Our findings suggest that careful experiment design and CPath-specific Stain Augmentation technique can be very effective. However, there is no one-size-fits-all solution for DG in CPath. Therefore, we establish clear guidelines for detecting and managing DS depending on different scenarios. While most of the concepts, guidelines, and recommendations are given for applications in CPath, we believe that they are applicable to most medical image analysis tasks as well.

Mimicking a Pathologist: Dual Attention Model for Scoring of Gigapixel Histology Images

Some major challenges associated with the automated processing of whole slide images (WSIs) includes their sheer size, different magnification levels and high resolution. Utilizing these images directly in AI frameworks is computationally expensive due to memory constraints, while downsampling WSIs incurs information loss and splitting WSIs into tiles and patches results in loss of important contextual information. We propose a novel dual attention approach, consisting of two main components, to mimic visual examination by a pathologist. The first component is a soft attention model which takes as input a high-level view of the WSI to determine various regions of interest. We employ a custom sampling method to extract diverse and spatially distinct image tiles from selected high attention areas. The second component is a hard attention classification model, which further extracts a sequence of multi-resolution glimpses from each tile for classification. Since hard attention is non-differentiable, we train this component using reinforcement learning and predict the location of glimpses without processing all patches of a given tile, thereby aligning with pathologist's way of diagnosis. We train our components both separately and in an end-to-end fashion using a joint loss function to demonstrate the efficacy of our proposed model. We employ our proposed model on two different IHC use cases: HER2 prediction on breast cancer and prediction of Intact/Loss status of two MMR biomarkers, for colorectal cancer. We show that the proposed model achieves accuracy comparable to state-of-the-art methods while only processing a small fraction of the WSI at highest magnification.

Cellular Segmentation and Composition in Routine Histology Images using Deep Learning

Identification and quantification of nuclei in colorectal cancer haematoxylin \& eosin (H\&E) stained histology images is crucial to prognosis and patient management. In computational pathology these tasks are referred to as nuclear segmentation, classification and composition and are used to extract meaningful interpretable cytological and architectural features for downstream analysis. The CoNIC challenge poses the task of automated nuclei segmentation, classification and composition into six different types of nuclei from the largest publicly known nuclei dataset - Lizard. In this regard, we have developed pipelines for the prediction of nuclei segmentation using HoVer-Net and ALBRT for cellular composition. On testing on the preliminary test set, HoVer-Net achieved a PQ of 0.58, a PQ+ of 0.58 and finally a mPQ+ of 0.35. For the prediction of cellular composition with ALBRT on the preliminary test set, we achieved an overall $R^2$ score of 0.53, consisting of 0.84 for lymphocytes, 0.70 for epithelial cells, 0.70 for plasma and .060 for eosinophils.