Ekaterina Redekop

Abhejit Rajagopal, Ekaterina Redekop, Anil Kemisetti et al.

Early prostate cancer detection and staging from MRI are extremely challenging tasks for both radiologists and deep learning algorithms, but the potential to learn from large and diverse datasets remains a promising avenue to increase their generalization capability both within- and across clinics. To enable this for prototype-stage algorithms, where the majority of existing research remains, in this paper we introduce a flexible federated learning framework for cross-site training, validation, and evaluation of deep prostate cancer detection algorithms. Our approach utilizes an abstracted representation of the model architecture and data, which allows unpolished prototype deep learning models to be trained without modification using the NVFlare federated learning framework. Our results show increases in prostate cancer detection and classification accuracy using a specialized neural network model and diverse prostate biopsy data collected at two University of California research hospitals, demonstrating the efficacy of our approach in adapting to different datasets and improving MR-biomarker discovery. We open-source our FLtools system, which can be easily adapted to other deep learning projects for medical imaging.

Ekaterina Redekop, Mara Pleasure, Zichen Wang et al.

Prostate cancer (PCa) was the most frequently diagnosed cancer among American men in 2023. The histological grading of biopsies is essential for diagnosis, and various deep learning-based solutions have been developed to assist with this task. Existing deep learning frameworks are typically applied to individual 2D cross-sections sliced from 3D biopsy tissue specimens. This process impedes the analysis of complex tissue structures such as glands, which can vary depending on the tissue slice examined. We propose a novel digital pathology data source called a "volumetric core," obtained via the extraction and co-alignment of serially sectioned tissue sections using a novel morphology-preserving alignment framework. We trained an attention-based multiple-instance learning (ABMIL) framework on deep features extracted from volumetric patches to automatically classify the Gleason Grade Group (GGG). To handle volumetric patches, we used a modified video transformer with a deep feature extractor pretrained using self-supervised learning. We ran our morphology-preserving alignment framework to construct 10,210 volumetric cores, leaving out 30% for pretraining. The rest of the dataset was used to train ABMIL, which resulted in a 0.958 macro-average AUC, 0.671 F1 score, 0.661 precision, and 0.695 recall averaged across all five GGG significantly outperforming the 2D baselines.

Ekaterina Redekop, Mara Pleasure, Zichen Wang et al.

The rapid growth of digital pathology and advances in self-supervised deep learning have enabled the development of foundational models for various pathology tasks across diverse diseases. While multimodal approaches integrating diverse data sources have emerged, a critical gap remains in the comprehensive integration of whole-slide images (WSIs) with spatial transcriptomics (ST), which is crucial for capturing critical molecular heterogeneity beyond standard hematoxylin & eosin (H&E) staining. We introduce SPADE, a foundation model that integrates histopathology with ST data to guide image representation learning within a unified framework, in effect creating an ST-informed latent space. SPADE leverages a mixture-of-data experts technique, where experts are created via two-stage imaging feature-space clustering using contrastive learning to learn representations of co-registered WSI patches and gene expression profiles. Pre-trained on the comprehensive HEST-1k dataset, SPADE is evaluated on 20 downstream tasks, demonstrating significantly superior few-shot performance compared to baseline models, highlighting the benefits of integrating morphological and molecular information into one latent space. Code and pretrained weights are available at https://github.com/uclabair/SPADE.

Ekaterina Redekop, Mara Pleasure, Vedrana Ivezic et al.

Foundation models in digital pathology use massive datasets to learn useful compact feature representations of complex histology images. However, there is limited transparency into what drives the correlation between dataset size and performance, raising the question of whether simply adding more data to increase performance is always necessary. In this study, we propose a prototype-guided diffusion model to generate high-fidelity synthetic pathology data at scale, enabling large-scale self-supervised learning and reducing reliance on real patient samples while preserving downstream performance. Using guidance from histological prototypes during sampling, our approach ensures biologically and diagnostically meaningful variations in the generated data. We demonstrate that self-supervised features trained on our synthetic dataset achieve competitive performance despite using ~60x-760x less data than models trained on large real-world datasets. Notably, models trained using our synthetic data showed statistically comparable or better performance across multiple evaluation metrics and tasks, even when compared to models trained on orders of magnitude larger datasets. Our hybrid approach, combining synthetic and real data, further enhanced performance, achieving top results in several evaluations. These findings underscore the potential of generative AI to create compelling training data for digital pathology, significantly reducing the reliance on extensive clinical datasets and highlighting the efficiency of our approach.

Ekaterina Redekop, Alexey Chernyavskiy

The development of high quality medical image segmentation algorithms depends on the availability of large datasets with pixel-level labels. The challenges of collecting such datasets, especially in case of 3D volumes, motivate to develop approaches that can learn from other types of labels that are cheap to obtain, e.g. bounding boxes. We focus on 3D medical images with their corresponding 3D bounding boxes which are considered as series of per-slice non-tight 2D bounding boxes. While current weakly-supervised approaches that use 2D bounding boxes as weak labels can be applied to medical image segmentation, we show that their success is limited in cases when the assumption about the tightness of the bounding boxes breaks. We propose a new bounding box correction framework which is trained on a small set of pixel-level annotations to improve the tightness of a larger set of non-tight bounding box annotations. The effectiveness of our solution is demonstrated by evaluating a known weakly-supervised segmentation approach with and without the proposed bounding box correction algorithm. When the tightness is improved by our solution, the results of the weakly-supervised segmentation become much closer to those of the fully-supervised one.

Ekaterina Redekop, Alexey Chernyavskiy

The success of modern deep learning algorithms for image segmentation heavily depends on the availability of large datasets with clean pixel-level annotations (masks), where the objects of interest are accurately delineated. Lack of time and expertise during data annotation leads to incorrect boundaries and label noise. It is known that deep convolutional neural networks (DCNNs) can memorize even completely random labels, resulting in poor accuracy. We propose a framework to train binary segmentation DCNNs using sets of unreliable pixel-level annotations. Erroneously labeled pixels are identified based on the estimated aleatoric uncertainty of the segmentation and are relabeled to the true value.