Rene Werner

Frederic Madesta, Thilo Sentker, Tobias Gauer et al.

4D CT imaging is an essential component of radiotherapy of thoracic/abdominal tumors. 4D CT images are, however, often affected by artifacts that compromise treatment planning quality. In this work, deep learning (DL)-based conditional inpainting is proposed to restore anatomically correct image information of artifact-affected areas. The restoration approach consists of a two-stage process: DL-based detection of common interpolation (INT) and double structure (DS) artifacts, followed by conditional inpainting applied to the artifact areas. In this context, conditional refers to a guidance of the inpainting process by patient-specific image data to ensure anatomically reliable results. The study is based on 65 in-house 4D CT images of lung cancer patients (48 with only slight artifacts, 17 with pronounced artifacts) and two publicly available 4D CT data sets that serve as independent external test sets. Automated artifact detection revealed a ROC-AUC of 0.99 for INT and of 0.97 for DS artifacts (in-house data). The proposed inpainting method decreased the average root mean squared error (RMSE) by 52%(INT) and 59% (DS) for the in-house data. For the external test data sets, the RMSE improvement is similar (50% and 59 %, respectively). Applied to 4D CT data with pronounced artifacts (not part of the training set), 72% of the detectable artifacts were removed. The results highlight the potential of DL-based inpainting for restoration of artifact-affected 4D CT data. Compared to recent 4D CT inpainting and restoration approaches, the proposed methodology illustrates the advantages of exploiting patient-specific prior image information.

David Lohr, Rene Werner

Clinical application of high-resolution diffusion MRI is hindered by hardware limitations and prohibitive scan times, motivating computational super-resolution. This study investigates the efficacy of a feature-based loss function in preserving diffusion signal consistency in deep learning super-resolution. Using 7T data from the human connectome project to generate pairs of low- and high-resolution diffusion weighted images (DWI), we trained UNets for 2D super-resolution. Ablation and isolation studies evaluated different VGG16-layers for feature-based losses against an image-based L1 baseline. Deeper layers and combinations thereof resulted in grid-like artifacts in super-resolution DWIs, which persisted in diffusion parameters like quantitative and fractional anisotropy. No such artifacts were present when using the shallowest layer. Downstream analysis for this layer showed great consistency with the ground truth, even for 9-fold super-resolution. Image SNR and used VGG16-layer depths modulated artifact appearance and severity, mandating careful selection of contributing layers for application in and beyond diffusion MRI.

Georgii Kolokolnikov, Marie-Lena Schmalhofer, Sophie Goetz et al.

Background and Objectives: Neurofibromatosis type 1 is a genetic disorder characterized by the development of numerous neurofibromas (NFs) throughout the body. Whole-body MRI (WB-MRI) is the clinical standard for detection and longitudinal surveillance of NF tumor growth. Existing interactive segmentation methods fail to combine high lesion-wise precision with scalability to hundreds of lesions. This study proposes a novel interactive segmentation model tailored to this challenge. Methods: We introduce MOIS-SAM2, a multi-object interactive segmentation model that extends the state-of-the-art, transformer-based, promptable Segment Anything Model 2 (SAM2) with exemplar-based semantic propagation. MOIS-SAM2 was trained and evaluated on 119 WB-MRI scans from 84 NF1 patients acquired using T2-weighted fat-suppressed sequences. The dataset was split at the patient level into a training set and four test sets (one in-domain and three reflecting different domain shift scenarios, e.g., MRI field strength variation, low tumor burden, differences in clinical site and scanner vendor). Results: On the in-domain test set, MOIS-SAM2 achieved a scan-wise DSC of 0.60 against expert manual annotations, outperforming baseline 3D nnU-Net (DSC: 0.54) and SAM2 (DSC: 0.35). Performance of the proposed model was maintained under MRI field strength shift (DSC: 0.53) and scanner vendor variation (DSC: 0.50), and improved in low tumor burden cases (DSC: 0.61). Lesion detection F1 scores ranged from 0.62 to 0.78 across test sets. Preliminary inter-reader variability analysis showed model-to-expert agreement (DSC: 0.62-0.68), comparable to inter-expert agreement (DSC: 0.57-0.69). Conclusions: The proposed MOIS-SAM2 enables efficient and scalable interactive segmentation of NFs in WB-MRI with minimal user input and strong generalization, supporting integration into clinical workflows.

Georgii Kolokolnikov, Marie-Lena Schmalhofer, Lennart Well et al.

Neurofibromatosis Type 1 is a genetic disorder characterized by the development of neurofibromas (NFs), which exhibit significant variability in size, morphology, and anatomical location. Accurate and automated segmentation of these tumors in whole-body magnetic resonance imaging (WB-MRI) is crucial to assess tumor burden and monitor disease progression. In this study, we present and analyze a fully automated pipeline for NF segmentation in fat-suppressed T2-weighted WB-MRI, consisting of three stages: anatomy segmentation, NF segmentation, and tumor candidate classification. In the first stage, we use the MRSegmentator model to generate an anatomy segmentation mask, extended with a high-risk zone for NFs. This mask is concatenated with the input image as anatomical context information for NF segmentation. The second stage employs an ensemble of 3D anisotropic anatomy-informed U-Nets to produce an NF segmentation confidence mask. In the final stage, tumor candidates are extracted from the confidence mask and classified based on radiomic features, distinguishing tumors from non-tumor regions and reducing false positives. We evaluate the proposed pipeline on three test sets representing different conditions: in-domain data (test set 1), varying imaging protocols and field strength (test set 2), and low tumor burden cases (test set 3). Experimental results show a 68% improvement in per-scan Dice Similarity Coefficient (DSC), a 21% increase in per-tumor DSC, and a two-fold improvement in F1 score for tumor detection in high tumor burden cases by integrating anatomy information. The method is integrated into the 3D Slicer platform for practical clinical use, with the code publicly accessible.