Johannes Kiechle

CV
h-index3
6papers
66citations
Novelty43%
AI Score46

6 Papers

8.7CVJul 10, 2024Code
Progressive Growing of Patch Size: Resource-Efficient Curriculum Learning for Dense Prediction Tasks

Stefan M. Fischer, Lina Felsner, Richard Osuala et al.

In this work, we introduce Progressive Growing of Patch Size, a resource-efficient implicit curriculum learning approach for dense prediction tasks. Our curriculum approach is defined by growing the patch size during model training, which gradually increases the task's difficulty. We integrated our curriculum into the nnU-Net framework and evaluated the methodology on all 10 tasks of the Medical Segmentation Decathlon. With our approach, we are able to substantially reduce runtime, computational costs, and CO2 emissions of network training compared to classical constant patch size training. In our experiments, the curriculum approach resulted in improved convergence. We are able to outperform standard nnU-Net training, which is trained with constant patch size, in terms of Dice Score on 7 out of 10 MSD tasks while only spending roughly 50% of the original training runtime. To the best of our knowledge, our Progressive Growing of Patch Size is the first successful employment of a sample-length curriculum in the form of patch size in the field of computer vision. Our code is publicly available at https://github.com/compai-lab/2024-miccai-fischer.

8.6IVNov 12, 2025Code
TomoGraphView: 3D Medical Image Classification with Omnidirectional Slice Representations and Graph Neural Networks

Johannes Kiechle, Stefan M. Fischer, Daniel M. Lang et al.

The growing number of medical tomography examinations has necessitated the development of automated methods capable of extracting comprehensive imaging features to facilitate downstream tasks such as tumor characterization, while assisting physicians in managing their growing workload. However, 3D medical image classification remains a challenging task due to the complex spatial relationships and long-range dependencies inherent in volumetric data. Training models from scratch suffers from low data regimes, and the absence of 3D large-scale multimodal datasets has limited the development of 3D medical imaging foundation models. Recent studies, however, have highlighted the potential of 2D vision foundation models, originally trained on natural images, as powerful feature extractors for medical image analysis. Despite these advances, existing approaches that apply 2D models to 3D volumes via slice-based decomposition remain suboptimal. Conventional volume slicing strategies, which rely on canonical planes such as axial, sagittal, or coronal, may inadequately capture the spatial extent of target structures when these are misaligned with standardized viewing planes. Furthermore, existing slice-wise aggregation strategies rarely account for preserving the volumetric structure, resulting in a loss of spatial coherence across slices. To overcome these limitations, we propose TomoGraphView, a novel framework that integrates omnidirectional volume slicing with spherical graph-based feature aggregation. We publicly share our accessible code base at http://github.com/compai-lab/2025-MedIA-kiechle and provide a user-friendly library for omnidirectional volume slicing at https://pypi.org/project/OmniSlicer.

6.4CVJul 6Code
Graph Representation Learning of Longitudinal Medical Imaging Trajectories for Treatment Response Prediction

Johannes Kiechle, Richard Osuala, Daniel M. Lang et al.

In patients with breast cancer, pathological complete response (pCR) has been established as a clinically meaningful surrogate marker for long-term outcomes. While commonly treated with neoadjuvant chemotherapy (NACT), effective treatment decision-making remains challenging, as therapeutic response can vary substantially across patients, calling for predictive models capable of accurately estimating individualized treatment response. To address this, we propose an imaging-based 3D spatio-temporal framework for treatment response prediction that integrates a state-of-the-art graph neural network with relational modeling of temporal interactions across timepoints alongside three novel complementary self-supervised treatment trajectory representation learning objectives. Experiments across a cohort of 585 patients from the public ISPY-2 dataset demonstrate that our method substantially outperforms both vision and self-supervised learning baselines across several classification metrics. Alongside establishing a breast cancer pCR prediction benchmark, we include a principled ablation of our method and further introduce and empirically assess the impact of the available number of DCE-MRI timepoints per patient trajectory and the inclusion of inter-scan time-differences. Overall, our study substantiates the utility of clinically meaningful longitudinal medical imagaging modeling for predicting NACT-induced pCR. We will publicly share our code repository and a user-friendly PyPI library for dataset curation upon publication, effectively promoting reproducible open-source research.

8.3LGJun 1
Entropy Minimization without Model Collapse: Mitigating Prediction Bias in Medical Imaging

Tim Nielen, Sameer Ambekar, Johannes Kiechle et al.

Entropy minimization (EM) is the dominant objective for test-time adaptation, yet its failure mode, model collapse, remains poorly understood. In this work, we show that distribution shifts can cause feature clusters corresponding to distinct classes in the model's representation space to merge, while the decision boundary remains fixed. This induces a systematic skew in the predicted class distribution, referred to as prediction bias. Prediction bias refers to a shift in the predicted class distribution, with some classes overrepresented and others suppressed. We show that entropy minimization amplifies this prediction bias by tightening the existing clusters, reinforcing the incorrect groupings until all predictions collapse to a trivial solution. Next, to demonstrate the significance of prediction bias and mitigate it, we further propose Distribution Shift Bias Reduction (DSBR), a bias-correcting objective that specifically targets this failure mode by equalizing the contribution of each predicted class to the unsupervised entropy minimization loss. To study this failure mode, we design suitable adaptation settings using four medical-imaging datasets and additionally evaluate on ImageNet-C. We find that DSBR consistently stabilizes test-time adaptation, prevents model collapse, and matches or outperforms state-of-the-art methods. Moreover, DSBR operates solely at test-time.

3.7CVMar 31, 2024Code
Disentangling Hippocampal Shape Variations: A Study of Neurological Disorders Using Mesh Variational Autoencoder with Contrastive Learning

Jakaria Rabbi, Johannes Kiechle, Christian Beaulieu et al.

This paper presents a comprehensive study focused on disentangling hippocampal shape variations from diffusion tensor imaging (DTI) datasets within the context of neurological disorders. Leveraging a Mesh Variational Autoencoder (VAE) enhanced with Supervised Contrastive Learning, our approach aims to improve interpretability by disentangling two distinct latent variables corresponding to age and the presence of diseases. In our ablation study, we investigate a range of VAE architectures and contrastive loss functions, showcasing the enhanced disentanglement capabilities of our approach. This evaluation uses synthetic 3D torus mesh data and real 3D hippocampal mesh datasets derived from the DTI hippocampal dataset. Our supervised disentanglement model outperforms several state-of-the-art (SOTA) methods like attribute and guided VAEs in terms of disentanglement scores. Our model distinguishes between age groups and disease status in patients with Multiple Sclerosis (MS) using the hippocampus data. Our Mesh VAE with Supervised Contrastive Learning shows the volume changes of the hippocampus of MS populations at different ages, and the result is consistent with the current neuroimaging literature. This research provides valuable insights into the relationship between neurological disorder and hippocampal shape changes in different age groups of MS populations using a Mesh VAE with Supervised Contrastive loss. Our code is available at https://github.com/Jakaria08/Explaining_Shape_Variability

5.2CVJun 20, 2024
Mask the Unknown: Assessing Different Strategies to Handle Weak Annotations in the MICCAI2023 Mediastinal Lymph Node Quantification Challenge

Stefan M. Fischer, Johannes Kiechle, Daniel M. Lang et al.

Pathological lymph node delineation is crucial in cancer diagnosis, progression assessment, and treatment planning. The MICCAI 2023 Lymph Node Quantification Challenge published the first public dataset for pathological lymph node segmentation in the mediastinum. As lymph node annotations are expensive, the challenge was formed as a weakly supervised learning task, where only a subset of all lymph nodes in the training set have been annotated. For the challenge submission, multiple methods for training on these weakly supervised data were explored, including noisy label training, loss masking of unlabeled data, and an approach that integrated the TotalSegmentator toolbox as a form of pseudo labeling in order to reduce the number of unknown voxels. Furthermore, multiple public TCIA datasets were incorporated into the training to improve the performance of the deep learning model. Our submitted model achieved a Dice score of 0.628 and an average symmetric surface distance of 5.8~mm on the challenge test set. With our submitted model, we accomplished third rank in the MICCAI2023 LNQ challenge. A finding of our analysis was that the integration of all visible, including non-pathological, lymph nodes improved the overall segmentation performance on pathological lymph nodes of the test set. Furthermore, segmentation models trained only on clinically enlarged lymph nodes, as given in the challenge scenario, could not generalize to smaller pathological lymph nodes. The code and model for the challenge submission are available at \url{https://gitlab.lrz.de/compai/MediastinalLymphNodeSegmentation}.