Mathias Prokop

Gabriel Efrain Humpire Mamani, Nikolas Lessmann, Ernst Th. Scholten et al.

In this study, we introduce a deep learning approach for segmenting kidney parenchyma and kidney abnormalities to support clinicians in identifying and quantifying renal abnormalities such as cysts, lesions, masses, metastases, and primary tumors. Our end-to-end segmentation method was trained on 215 contrast-enhanced thoracic-abdominal CT scans, with half of these scans containing one or more abnormalities. We began by implementing our own version of the original 3D U-Net network and incorporated four additional components: an end-to-end multi-resolution approach, a set of task-specific data augmentations, a modified loss function using top-$k$, and spatial dropout. Furthermore, we devised a tailored post-processing strategy. Ablation studies demonstrated that each of the four modifications enhanced kidney abnormality segmentation performance, while three out of four improved kidney parenchyma segmentation. Subsequently, we trained the nnUNet framework on our dataset. By ensembling the optimized 3D U-Net and the nnUNet with our specialized post-processing, we achieved marginally superior results. Our best-performing model attained Dice scores of 0.965 and 0.947 for segmenting kidney parenchyma in two test sets (20 scans without abnormalities and 30 with abnormalities), outperforming an independent human observer who scored 0.944 and 0.925, respectively. In segmenting kidney abnormalities within the 30 test scans containing them, the top-performing method achieved a Dice score of 0.585, while an independent second human observer reached a score of 0.664, suggesting potential for further improvement in computerized methods. All training data is available to the research community under a CC-BY 4.0 license on https://doi.org/10.5281/zenodo.8014289

Gabriel Efrain Humpire-Mamani, Colin Jacobs, Mathias Prokop et al.

Transfer learning leverages pre-trained model features from a large dataset to save time and resources when training new models for various tasks, potentially enhancing performance. Due to the lack of large datasets in the medical imaging domain, transfer learning from one medical imaging model to other medical imaging models has not been widely explored. This study explores the use of transfer learning to improve the performance of deep convolutional neural networks for organ segmentation in medical imaging. A base segmentation model (3D U-Net) was trained on a large and sparsely annotated dataset; its weights were used for transfer learning on four new down-stream segmentation tasks for which a fully annotated dataset was available. We analyzed the training set size's influence to simulate scarce data. The results showed that transfer learning from the base model was beneficial when small datasets were available, providing significant performance improvements; where fine-tuning the base model is more beneficial than updating all the network weights with vanilla transfer learning. Transfer learning with fine-tuning increased the performance by up to 0.129 (+28\%) Dice score than experiments trained from scratch, and on average 23 experiments increased the performance by 0.029 Dice score in the new segmentation tasks. The study also showed that cross-modality transfer learning using CT scans was beneficial. The findings of this study demonstrate the potential of transfer learning to improve the efficiency of annotation and increase the accessibility of accurate organ segmentation in medical imaging, ultimately leading to improved patient care. We made the network definition and weights publicly available to benefit other users and researchers.

Michelle Stegeman, Lena Philipp, Fennie van der Graaf et al.

Medical foundation models show promise to learn broadly generalizable features from large, diverse datasets. This could be the base for reliable cross-modality generalization and rapid adaptation to new, task-specific goals, with only a few task-specific examples. Yet, evidence for this is limited by the lack of public, standardized, and reproducible evaluation frameworks, as existing public benchmarks are often fragmented across task-, organ-, or modality-specific settings, limiting assessment of cross-task generalization. We introduce UNICORN, a public benchmark designed to systematically evaluate medical foundation models under a unified protocol. To isolate representation quality, we built the benchmark on a novel two-step framework that decouples model inference from task-specific evaluation based on standardized few-shot adaptation. As a central design choice, we constructed indirectly accessible sequestered test sets derived from clinically relevant cohorts, along with standardized evaluation code and a submission interface on an open benchmarking platform. Performance is aggregated into a single UNICORN Score, a new metric that we introduce to support direct comparison of foundation models across diverse medical domains, modalities, and task types. The UNICORN test dataset includes data from more than 2,400 patients, including over 3,700 vision cases and over 2,400 clinical reports collected from 17 institutions across eight countries. The benchmark spans eight anatomical regions and four imaging modalities. Both task-specific and aggregated leaderboards enable accessible, standardized, and reproducible evaluation. By standardizing multi-task, multi-modality assessment, UNICORN establishes a foundation for reproducible benchmarking of medical foundation models. Data, baseline methods, and the evaluation platform are publicly available via unicorn.grand-challenge.org.

Hartmut Häntze, Lina Xu, Christian J. Mertens et al.

Purpose: To develop and evaluate a deep learning model for multi-organ segmentation of MRI scans. Materials and Methods: The model was trained on 1,200 manually annotated 3D axial MRI scans from the UK Biobank, 221 in-house MRI scans, and 1228 CT scans from the TotalSegmentator dataset. A human-in-the-loop annotation workflow was employed, leveraging cross-modality transfer learning from an existing CT segmentation model to segment 40 anatomical structures. The annotation process began with a model based on transfer learning between CT and MR, which was iteratively refined based on manual corrections to predicted segmentations. The model's performance was evaluated on MRI examinations obtained from the German National Cohort (NAKO) study (n=900) from the AMOS22 dataset (n=60) and from the TotalSegmentator-MRI test data (n=29). The Dice Similarity Coefficient (DSC) and Hausdorff Distance (HD) were used to assess segmentation quality, stratified by organ and scan type. The model and its weights will be open-sourced. Results: MRSegmentator demonstrated high accuracy for well-defined organs (lungs: DSC 0.96, heart: DSC 0.94) and organs with anatomic variability (liver: DSC 0.96, kidneys: DSC 0.95). Smaller structures showed lower accuracy (portal/splenic veins: DSC 0.64, adrenal glands: DSC 0.69). On external validation using NAKO data, mean DSC ranged from 0.85 $\pm$ 0.08 for T2-HASTE to 0.91 $\pm$ 0.05 for in-phase sequences. The model generalized well to CT, achieving mean DSC of 0.84 $\pm$ 0.11 on AMOS CT data. Conclusion: MRSegmentator accurately segments 40 anatomical structures in MRI across diverse datasets and imaging protocols, with additional generalizability to CT images. This open-source model will provide a valuable tool for automated multi-organ segmentation in medical imaging research. It can be downloaded from https://github.com/hhaentze/MRSegmentator.

Luc Builtjes, Joeran Bosma, Mathias Prokop et al.

Medical reports contain rich clinical information but are often unstructured and written in domain-specific language, posing challenges for information extraction. While proprietary large language models (LLMs) have shown promise in clinical natural language processing, their lack of transparency and data privacy concerns limit their utility in healthcare. This study therefore evaluates nine open-source generative LLMs on the DRAGON benchmark, which includes 28 clinical information extraction tasks in Dutch. We developed \texttt{llm\_extractinator}, a publicly available framework for information extraction using open-source generative LLMs, and used it to assess model performance in a zero-shot setting. Several 14 billion parameter models, Phi-4-14B, Qwen-2.5-14B, and DeepSeek-R1-14B, achieved competitive results, while the bigger Llama-3.3-70B model achieved slightly higher performance at greater computational cost. Translation to English prior to inference consistently degraded performance, highlighting the need of native-language processing. These findings demonstrate that open-source LLMs, when used with our framework, offer effective, scalable, and privacy-conscious solutions for clinical information extraction in low-resource settings.

Sarah de Boer, Hartmut Häntze, Kiran Vaidhya Venkadesh et al.

Kidney abnormality segmentation has important potential to enhance the clinical workflow, especially in settings requiring quantitative assessments. Kidney volume could serve as an important biomarker for renal diseases, with changes in volume correlating directly with kidney function. Currently, clinical practice often relies on subjective visual assessment for evaluating kidney size and abnormalities, including tumors and cysts, which are typically staged based on diameter, volume, and anatomical location. To support a more objective and reproducible approach, this research aims to develop a robust, thoroughly validated kidney abnormality segmentation algorithm, made publicly available for clinical and research use. We employ publicly available training datasets and leverage the state-of-the-art medical image segmentation framework nnU-Net. Validation is conducted using both proprietary and public test datasets, with segmentation performance quantified by Dice coefficient and the 95th percentile Hausdorff distance. Furthermore, we analyze robustness across subgroups based on patient sex, age, CT contrast phases, and tumor histologic subtypes. Our findings demonstrate that our segmentation algorithm, trained exclusively on publicly available data, generalizes effectively to external test sets and outperforms existing state-of-the-art models across all tested datasets. Subgroup analyses reveal consistent high performance, indicating strong robustness and reliability. The developed algorithm and associated code are publicly accessible at https://github.com/DIAGNijmegen/oncology-kidney-abnormality-segmentation.

Xuan Loc Pham, Mathias Prokop, Bram van Ginneken et al.

Image registration is an essential technique for the analysis of Computed Tomography (CT) images in clinical practice. However, existing methodologies are predominantly tailored to a specific organ of interest and often exhibit lower performance on other organs, thus limiting their generalizability and applicability. Multi-organ registration addresses these limitations, but the simultaneous alignment of multiple organs with diverse shapes, sizes and locations requires a highly complex deformation field with a multi-layer composition of individual deformations. This study introduces a novel field decomposition approach to address the high complexity of deformations in multi-organ whole-body CT image registration. The proposed method is trained and evaluated on a longitudinal dataset of 691 patients, each with two CT images obtained at distinct time points. These scans fully encompass the thoracic, abdominal, and pelvic regions. Two baseline registration methods are selected for this study: one based on optimization techniques and another based on deep learning. Experimental results demonstrate that the proposed approach outperforms baseline methods in handling complex deformations in multi-organ whole-body CT image registration.

Niels Rocholl, Ewoud Smit, Mathias Prokop et al.

Longitudinal lesion analysis is crucial for oncological care, yet automated tools often struggle with temporal consistency. While universal lesion segmentation models have advanced, they are typically designed for single time points. This paper investigates the performance of the ULS23 segmentation model in a longitudinal context. Using a public clinical dataset of baseline and follow-up CT scans, we evaluated the model's ability to segment and track lesions over time. We identified two critical, interconnected failure modes: a sharp degradation in segmentation quality in follow-up cases due to inter-scan registration errors, and a subsequent breakdown of the lesion correspondence process. To systematically probe this vulnerability, we conducted a controlled experiment where we artificially displaced the input volume relative to the true lesion center. Our results demonstrate that the model's performance is highly dependent on its assumption of a centered lesion; segmentation accuracy collapses when the lesion is sufficiently displaced. These findings reveal a fundamental limitation of applying single-timepoint models to longitudinal data. We conclude that robust oncological tracking requires a paradigm shift away from cascading single-purpose tools towards integrated, end-to-end models inherently designed for temporal analysis.

M. J. J. de Grauw, E. Th. Scholten, E. J. Smit et al.

Size measurements of tumor manifestations on follow-up CT examinations are crucial for evaluating treatment outcomes in cancer patients. Efficient lesion segmentation can speed up these radiological workflows. While numerous benchmarks and challenges address lesion segmentation in specific organs like the liver, kidneys, and lungs, the larger variety of lesion types encountered in clinical practice demands a more universal approach. To address this gap, we introduced the ULS23 benchmark for 3D universal lesion segmentation in chest-abdomen-pelvis CT examinations. The ULS23 training dataset contains 38,693 lesions across this region, including challenging pancreatic, colon and bone lesions. For evaluation purposes, we curated a dataset comprising 775 lesions from 284 patients. Each of these lesions was identified as a target lesion in a clinical context, ensuring diversity and clinical relevance within this dataset. The ULS23 benchmark is publicly accessible via uls23.grand-challenge.org, enabling researchers worldwide to assess the performance of their segmentation methods. Furthermore, we have developed and publicly released our baseline semi-supervised 3D lesion segmentation model. This model achieved an average Dice coefficient of 0.703 $\pm$ 0.240 on the challenge test set. We invite ongoing submissions to advance the development of future ULS models.

Ecem Sogancioglu, Keelin Murphy, Ernst Th. Scholten et al.

Total lung volume is an important quantitative biomarker and is used for the assessment of restrictive lung diseases. In this study, we investigate the performance of several deep-learning approaches for automated measurement of total lung volume from chest radiographs. 7621 posteroanterior and lateral view chest radiographs (CXR) were collected from patients with chest CT available. Similarly, 928 CXR studies were chosen from patients with pulmonary function test (PFT) results. The reference total lung volume was calculated from lung segmentation on CT or PFT data, respectively. This dataset was used to train deep-learning architectures to predict total lung volume from chest radiographs. The experiments were constructed in a step-wise fashion with increasing complexity to demonstrate the effect of training with CT-derived labels only and the sources of error. The optimal models were tested on 291 CXR studies with reference lung volume obtained from PFT. The optimal deep-learning regression model showed an MAE of 408 ml and a MAPE of 8.1\% and Pearson's r = 0.92 using both frontal and lateral chest radiographs as input. CT-derived labels were useful for pre-training but the optimal performance was obtained by fine-tuning the network with PFT-derived labels. We demonstrate, for the first time, that state-of-the-art deep learning solutions can accurately measure total lung volume from plain chest radiographs. The proposed model can be used to obtain total lung volume from routinely acquired chest radiographs at no additional cost and could be a useful tool to identify trends over time in patients referred regularly for chest x-rays.