Computerized assessment of background parenchymal enhancement on breast dynamic contrast-enhanced-MRI including electronic lesion removal.

Purpose: Current clinical assessment qualitatively describes background parenchymal enhancement (BPE) as minimal, mild, moderate, or marked based on the visually perceived volume and intensity of enhancement in normal fibroglandular breast tissue in dynamic contrast-enhanced (DCE)-MRI. Tumor enhancement may be included within the visual assessment of BPE, thus inflating BPE estimation due to angiogenesis within the tumor. Using a dataset of 426 MRIs, we developed an automated method to segment breasts, electronically remove lesions, and calculate scores to estimate BPE levels. Approach: A U-Net was trained for breast segmentation from DCE-MRI maximum intensity projection (MIP) images. Fuzzy c-means clustering was used to segment lesions; the lesion volume was removed prior to creating projections. U-Net outputs were applied to create projection images of both, affected, and unaffected breasts before and after lesion removal. BPE scores were calculated from various projection images, including MIPs or average intensity projections of first- or second postcontrast subtraction MRIs, to evaluate the effect of varying image parameters on automatic BPE assessment. Receiver operating characteristic analysis was performed to determine the predictive value of computed scores in BPE level classification tasks relative to radiologist ratings. Results: Statistically significant trends were found between radiologist BPE ratings and calculated BPE scores for all breast regions (Kendall correlation, p<0.001). Scores from all breast regions performed significantly better than guessing (p<0.025 from the z-test). Results failed to show a statistically significant difference in performance with and without lesion removal. BPE scores of the affected breast in the second postcontrast subtraction MIP after lesion removal performed statistically greater than random guessing across various viewing projections and DCE time points. Conclusions: Results demonstrate the potential for automatic BPE scoring to serve as a quantitative value for objective BPE level classification from breast DCE-MR without the influence of lesion enhancement.

Evaluation of emphysema on thoracic low-dose CTs through attention-based multiple instance deep learning.

In addition to lung cancer, other thoracic abnormalities, such as emphysema, can be visualized within low-dose CT scans that were initially obtained in cancer screening programs, and thus, opportunistic evaluation of these diseases may be highly valuable. However, manual assessment for each scan is tedious and often subjective, thus we have developed an automatic, rapid computer-aided diagnosis system for emphysema using attention-based multiple instance deep learning and 865 LDCTs. In the task of determining if a CT scan presented with emphysema or not, our novel Transfer AMIL approach yielded an area under the ROC curve of 0.94 ± 0.04, which was a statistically significant improvement compared to other methods evaluated in our study following the Delong Test with correction for multiple comparisons. Further, from our novel attention weight curves, we found that the upper lung demonstrated a stronger influence in all scan classes, indicating that the model prioritized upper lobe information. Overall, our novel Transfer AMIL method yielded high performance and provided interpretable information by identifying slices that were most influential to the classification decision, thus demonstrating strong potential for clinical implementation.

MIDRC CRP10 AI interface-an integrated tool for exploring, testing and visualization of AI models.

Objective. Developing Machine Learning models (N Gorre et al 2023) for clinical applications from scratch can be a cumbersome task requiring varying levels of expertise. Seasoned developers and researchers may also often face incompatible frameworks and data preparation issues. This is further complicated in the context of diagnostic radiology and oncology applications, given the heterogenous nature of the input data and the specialized task requirements. Our goal is to provide clinicians, researchers, and early AI developers with a modular, flexible, and user-friendly software tool that can effectively meet their needs to explore, train, and test AI algorithms by allowing users to interpret their model results. This latter step involves the incorporation of interpretability and explainability methods that would allow visualizing performance as well as interpreting predictions across the different neural network layers of a deep learning algorithm.Approach. To demonstrate our proposed tool, we have developed the CRP10 AI Application Interface (CRP10AII) as part of the MIDRC consortium. CRP10AII is based on the web service Django framework in Python. CRP10AII/Django/Python in combination with another data manager tool/platform, data commons such as Gen3 can provide a comprehensive while easy to use machine/deep learning analytics tool. The tool allows to test, visualize, interpret how and why the deep learning model is performing. The major highlight of CRP10AII is its capability of visualization and interpretability of otherwise Blackbox AI algorithms.Results. CRP10AII provides many convenient features for model building and evaluation, including: (1) query and acquire data according to the specific application (e.g. classification, segmentation) from the data common platform (Gen3 here); (2) train the AI models from scratch or use pre-trained models (e.g. VGGNet, AlexNet, BERT) for transfer learning and test the model predictions, performance assessment, receiver operating characteristics curve evaluation; (3) interpret the AI model predictions using methods like SHAPLEY, LIME values; and (4) visualize the model learning through heatmaps and activation maps of individual layers of the neural network.Significance. Unexperienced users may have more time to swiftly pre-process, build/train their AI models on their own use-cases, and further visualize and explore these AI models as part of this pipeline, all in an end-to-end manner. CRP10AII will be provided as an open-source tool, and we expect to continue developing it based on users' feedback.