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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., Comment: 17 pages, 6 figures; updated data; completed co-author info

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.

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

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., Comment: Under review

Automatic detection of pulmonary nodules in thoracic computed tomography (CT) scans has been an active area of research for the last two decades. However, there have only been few studies that provide a comparative performance evaluation of different systems on a common database. We have therefore set up the LUNA16 challenge, an objective evaluation framework for automatic nodule detection algorithms using the largest publicly available reference database of chest CT scans, the LIDC-IDRI data set. In LUNA16, participants develop their algorithm and upload their predictions on 888 CT scans in one of the two tracks: 1) the complete nodule detection track where a complete CAD system should be developed, or 2) the false positive reduction track where a provided set of nodule candidates should be classified. This paper describes the setup of LUNA16 and presents the results of the challenge so far. Moreover, the impact of combining individual systems on the detection performance was also investigated. It was observed that the leading solutions employed convolutional networks and used the provided set of nodule candidates. The combination of these solutions achieved an excellent sensitivity of over 95% at fewer than 1.0 false positives per scan. This highlights the potential of combining algorithms to improve the detection performance. Our observer study with four expert readers has shown that the best system detects nodules that were missed by expert readers who originally annotated the LIDC-IDRI data. We released this set of additional nodules for further development of CAD systems.

The introduction of lung cancer screening programs will produce an unprecedented amount of chest CT scans in the near future, which radiologists will have to read in order to decide on a patient follow-up strategy. According to the current guidelines, the workup of screen-detected nodules strongly relies on nodule size and nodule type. In this paper, we present a deep learning system based on multi-stream multi-scale convolutional networks, which automatically classifies all nodule types relevant for nodule workup. The system processes raw CT data containing a nodule without the need for any additional information such as nodule segmentation or nodule size and learns a representation of 3D data by analyzing an arbitrary number of 2D views of a given nodule. The deep learning system was trained with data from the Italian MILD screening trial and validated on an independent set of data from the Danish DLCST screening trial. We analyze the advantage of processing nodules at multiple scales with a multi-stream convolutional network architecture, and we show that the proposed deep learning system achieves performance at classifying nodule type that surpasses the one of classical machine learning approaches and is within the inter-observer variability among four experienced human observers., Comment: Published on Scientific Reports