Thomas Helbich

Mohammed Kamran, Maria Bernathova, Raoul Varga et al.

Accurate segmentation of small lesions in Breast Dynamic Contrast-Enhanced MRI (DCE-MRI) is critical for early cancer detection, especially in high-risk patients. While recent deep learning methods have advanced lesion segmentation, they primarily target large lesions and neglect valuable longitudinal and clinical information routinely used by radiologists. In real-world screening, detecting subtle or emerging lesions requires radiologists to compare across timepoints and consider previous radiology assessments, such as the BI-RADS score. We propose LesiOnTime, a novel 3D segmentation approach that mimics clinical diagnostic workflows by jointly leveraging longitudinal imaging and BIRADS scores. The key components are: (1) a Temporal Prior Attention (TPA) block that dynamically integrates information from previous and current scans; and (2) a BI-RADS Consistency Regularization (BCR) loss that enforces latent space alignment for scans with similar radiological assessments, thus embedding domain knowledge into the training process. Evaluated on a curated in-house longitudinal dataset of high-risk patients with DCE-MRI, our approach outperforms state-of-the-art single-timepoint and longitudinal baselines by 5% in terms of Dice. Ablation studies demonstrate that both TPA and BCR contribute complementary performance gains. These results highlight the importance of incorporating temporal and clinical context for reliable early lesion segmentation in real-world breast cancer screening. Our code is publicly available at https://github.com/cirmuw/LesiOnTime

Christoph Fürböck, Paul Weiser, Branko Mitic et al.

In real world clinical environments, training and applying deep learning models on multi-modal medical imaging data often struggles with partially incomplete data. Standard approaches either discard missing samples, require imputation or repurpose dropout learning schemes, limiting robustness and generalizability. To address this, we propose a hypernetwork-based method that dynamically generates task-specific classification models conditioned on the set of available modalities. Instead of training a fixed model, a hypernetwork learns to predict the parameters of a task model adapted to available modalities, enabling training and inference on all samples, regardless of completeness. We compare this approach with (1) models trained only on complete data, (2) state of the art channel dropout methods, and (3) an imputation-based method, using artificially incomplete datasets to systematically analyze robustness to missing modalities. Results demonstrate superior adaptability of our method, outperforming state of the art approaches with an absolute increase in accuracy of up to 8% when trained on a dataset with 25% completeness (75% of training data with missing modalities). By enabling a single model to generalize across all modality configurations, our approach provides an efficient solution for real-world multi-modal medical data analysis.

Ignacio Alvarez Illan, Javier Ramirez, Juan M. Gorriz et al.

Non-mass enhancing lesions (NME) constitute a diagnostic challenge in dynamic contrast enhanced magnetic resonance imaging (DCE-MRI) of the breast. Computer Aided Diagnosis (CAD) systems provide physicians with advanced tools for analysis, assessment and evaluation that have a significant impact on the diagnostic performance. Here, we propose a new approach to address the challenge of NME detection and segmentation, taking advantage of independent component analysis (ICA) to extract data-driven dynamic lesion characterizations. A set of independent sources was obtained from DCE-MRI dataset of breast patients, and the dynamic behavior of the different tissues was described by multiple dynamic curves, together with a set of eigenimages describing the scores for each voxel. A new test image is projected onto the independent source space using the unmixing matrix, and each voxel is classified by a support vector machine (SVM) that has already been trained with manually delineated data. A solution to the high false positive rate problem is proposed by controlling the SVM hyperplane location, outperforming previously published approaches.