Pathological complete response (pCR) can guide surgical strategy and postoperative treatments in triple-negative breast cancer (TNBC). In this study, we developed a Breast Cancer Response Prediction (BCRP) model to predict the pCR in patients with TNBC. The BCRP model integrated multi-dimensional longitudinal quantitative imaging features, clinical factors and features from the Breast Imaging Data and Reporting System (BI-RADS). Multi-dimensional longitudinal quantitative imaging features, including deep learning features and radiomics features, were extracted from multiview B-mode and colour Doppler ultrasound images before and after treatment. The BCRP model achieved the areas under the receiver operating curves (AUCs) of 0.94 [95% confidence interval (CI), 0.91-0.98] and 0.84 [95%CI, 0.75-0.92] in the training and external test cohorts, respectively. Additionally, the low BCRP score was an independent risk factor for event-free survival (P < 0.05). The BCRP model showed a promising ability in predicting response to neoadjuvant chemotherapy in TNBC, and could provide valuable information for survival.

Advances in magnetic resonance imaging (MRI) have revolutionized disease detection and treatment planning. However, the growing volume and complexity of MRI data-along with heterogeneity in imaging protocols, scanner technology, and labeling practices-creates a need for standardized tools to automatically identify and characterize key imaging attributes. Such tools are essential for large-scale, multi-institutional studies that rely on harmonized data to train robust machine learning models. In this study, we developed convolutional neural networks (CNNs) to automatically classify three core attributes of abdominal MRI: pulse sequence type, imaging orientation, and contrast enhancement status. Three distinct CNNs with similar backbone architectures were trained to classify single image slices into one of 12 pulse sequences, 4 orientations, or 2 contrast classes. The models achieved high classification accuracies of 99.51%, 99.87%, and 99.99% for pulse sequence, orientation, and contrast, respectively. We applied Grad-CAM to visualize image regions influencing pulse sequence predictions and highlight relevant anatomical features. To enhance performance, we implemented a majority voting approach to aggregate slice-level predictions, achieving 100% accuracy at the volume level for all tasks. External validation using the Duke Liver Dataset demonstrated strong generalizability; after adjusting for class label mismatch, volume-level accuracies exceeded 96.9% across all classification tasks.

Photon counting detector CT myelography is an effective modality for the localization of spinal CSF leaks. The initial studies describing this technique employed a relatively smooth Br56 kernel. However, subsequent studies have demonstrated that the use of the sharpest quantitative kernel on photon counting CT (Qr89), particularly when denoised with techniques such as quantum iterative reconstruction or convolutional neural networks, enhances detection of CSF-venous fistulas. In this clinical report, we sought to determine whether the Qr89 kernel has utility in patients with dural tears, the other main type of spinal CSF leak. We performed a retrospective review of patients with dural tears diagnosed on photon counting CT myelography, comparing Br56, Qr89 denoised with quantum iterative reconstruction, and Qr89 denoised with a trained convolutional neural network. We specifically assessed spatial resolution, noise level, and diagnostic confidence in eight such cases, finding that the sharper Qr89 kernel outperformed the smoother Br56 kernel. This was particularly true when Qr89 was denoised using a convolutional neural network. Furthermore, in two cases, the dural tear was only seen on the Qr89 reconstructions and missed on the Br56 kernel. Overall, our study demonstrates the potential value of further optimizing post-processing techniques for photon counting CT myelography aimed at localizing dural tears.ABBREVIATIONS: CNN = convolutional neural network; CVF = CSF-venous fistula; DSM = digital subtraction myelography; EID = energy integrating detector; PCD = photon counting detector; QIR = quantum iterative reconstruction.

The integration of pathology and radiology in medical imaging has emerged as a critical need for advancing diagnostic accuracy and improving clinical workflows. Current AI-driven approaches for medical image analysis, despite significant progress, face several challenges, including handling multi-modal imaging, imbalanced datasets, and the lack of robust interpretability and uncertainty quantification. These limitations often hinder the deployment of AI systems in real-world clinical settings, where reliability and adaptability are essential. To address these issues, this study introduces a novel framework, the Domain-Informed Adaptive Network (DIANet), combined with an Adaptive Clinical Workflow Integration (ACWI) strategy. DIANet leverages multi-scale feature extraction, domain-specific priors, and Bayesian uncertainty modeling to enhance interpretability and robustness. The proposed model is tailored for multi-modal medical imaging tasks, integrating adaptive learning mechanisms to mitigate domain shifts and imbalanced datasets. Complementing the model, the ACWI strategy ensures seamless deployment through explainable AI (XAI) techniques, uncertainty-aware decision support, and modular workflow integration compatible with clinical systems like PACS. Experimental results demonstrate significant improvements in diagnostic accuracy, segmentation precision, and reconstruction fidelity across diverse imaging modalities, validating the potential of this framework to bridge the gap between AI innovation and clinical utility.

&#xD;Intrathoracic airway segmentation in computed tomography (CT) is important for quantitative and qualitative analysis of various chronic respiratory diseases and bronchial surgery navigation. However, the airway tree's morphological complexity, incomplete labels resulting from annotation difficulty, and intra-class imbalance between main and terminal airways limit the segmentation performance.&#xD;Methods:&#xD;Three methodological improvements are proposed to deal with the challenges. Firstly, we design a DCT-UNet to collect better information on neighbouring voxels and ones within a larger spatial region. Secondly, an airway label self-updating (ALSU) strategy is proposed to iteratively update the reference labels to conquer the problem of incomplete labels. Thirdly, a deep learning-based terminal region growing (TRG) is adopted to extract terminal airways. Extensive experiments were conducted on two internal datasets and three public datasets.&#xD;Results:&#xD;Compared to the counterparts, the proposed method can achieve a higher Branch Detected, Tree-length Detected, Branch Ratio, and Tree-length Ratio (ISICDM2021 dataset, 95.19%, 94.89%, 166.45%, and 172.29%; BAS dataset, 96.03%, 95.11%, 129.35%, and 137.00%). Ablation experiments show the effectiveness of three proposed solutions. Our method is applied to an in-house Chorionic Obstructive Pulmonary Disease (COPD) dataset. The measures of branch count, tree length, endpoint count, airway volume, and airway surface area are significantly different between COPD severity stages.&#xD;Conclusions:&#xD;The proposed methods can segment more terminal bronchi and larger length of airway, even some bronchi which are real but missed in the manual annotation can be detected. Potential application significance has been presented in characterizing COPD airway lesions and severity stages.&#xD.

Medical image segmentation continues to advance rapidly, yet rigorous comparison between methods remains challenging due to a lack of standardized and customizable tooling. In this work, we present the current state of the Medical Imaging Segmentation Toolkit (MIST), with a particular focus on its flexible and modular postprocessing framework designed for the BraTS 2025 pre- and post-treatment glioma segmentation challenge. Since its debut in the 2024 BraTS adult glioma post-treatment segmentation challenge, MIST's postprocessing module has been significantly extended to support a wide range of transforms, including removal or replacement of small objects, extraction of the largest connected components, and morphological operations such as hole filling and closing. These transforms can be composed into user-defined strategies, enabling fine-grained control over the final segmentation output. We evaluate three such strategies - ranging from simple small-object removal to more complex, class-specific pipelines - and rank their performance using the BraTS ranking protocol. Our results highlight how MIST facilitates rapid experimentation and targeted refinement, ultimately producing high-quality segmentations for the BraTS 2025 challenge. MIST remains open source and extensible, supporting reproducible and scalable research in medical image segmentation.

Conventional multimodal data integration methods provide a comprehensive assessment of the shared or unique structure within each individual data type but suffer from several limitations such as the inability to handle high-dimensional data and identify nonlinear structures. In this paper, we introduce DeepJIVE, a deep-learning approach to performing Joint and Individual Variance Explained (JIVE). We perform mathematical derivation and experimental validations using both synthetic and real-world 1D, 2D, and 3D datasets. Different strategies of achieving the identity and orthogonality constraints for DeepJIVE were explored, resulting in three viable loss functions. We found that DeepJIVE can successfully uncover joint and individual variations of multimodal datasets. Our application of DeepJIVE to the Alzheimer's Disease Neuroimaging Initiative (ADNI) also identified biologically plausible covariation patterns between the amyloid positron emission tomography (PET) and magnetic resonance (MR) images. In conclusion, the proposed DeepJIVE can be a useful tool for multimodal data analysis.

Data scarcity is a major challenge in medical imaging, particularly for deep learning models. While data pooling (combining datasets from multiple sources) and data addition (adding more data from a new dataset) have been shown to enhance model performance, they are not without complications. Specifically, increasing the size of the training dataset through pooling or addition can induce distributional shifts, negatively affecting downstream model performance, a phenomenon known as the "Data Addition Dilemma". While the traditional i.i.d. assumption may not hold in multi-source contexts, assuming exchangeability across datasets provides a more practical framework for data pooling. In this work, we investigate medical image segmentation under these conditions, drawing insights from causal frameworks to propose a method for controlling foreground-background feature discrepancies across all layers of deep networks. This approach improves feature representations, which are crucial in data-addition scenarios. Our method achieves state-of-the-art segmentation performance on histopathology and ultrasound images across five datasets, including a novel ultrasound dataset that we have curated and contributed. Qualitative results demonstrate more refined and accurate segmentation maps compared to prominent baselines across three model architectures. The code will be available on Github.

Precise and automated segmentation of the liver and its tumor within CT scans plays a pivotal role in swift diagnosis and the development of optimal treatment plans for individuals with liver diseases and malignancies. However, automated liver and tumor segmentation faces significant hurdles arising from the inherent heterogeneity of tumors and the diverse visual characteristics of livers across a broad spectrum of patients. Aiming to address these challenges, we present a novel Transformer-aware Multiscale Progressive Encoder-Decoder Network (T-MPEDNet) for automated segmentation of tumor and liver. T-MPEDNet leverages a deep adaptive features backbone through a progressive encoder-decoder structure, enhanced by skip connections for recalibrating channel-wise features while preserving spatial integrity. A Transformer-inspired dynamic attention mechanism captures long-range contextual relationships within the spatial domain, further enhanced by multi-scale feature utilization for refined local details, leading to accurate prediction. Morphological boundary refinement is then employed to address indistinct boundaries with neighboring organs, capturing finer details and yielding precise boundary labels. The efficacy of T-MPEDNet is comprehensively assessed on two widely utilized public benchmark datasets, LiTS and 3DIRCADb. Extensive quantitative and qualitative analyses demonstrate the superiority of T-MPEDNet compared to twelve state-of-the-art methods. On LiTS, T-MPEDNet achieves outstanding Dice Similarity Coefficients (DSC) of 97.6% and 89.1% for liver and tumor segmentation, respectively. Similar performance is observed on 3DIRCADb, with DSCs of 98.3% and 83.3% for liver and tumor segmentation, respectively. Our findings prove that T-MPEDNet is an efficacious and reliable framework for automated segmentation of the liver and its tumor in CT scans.

Purpose: To develop a reconstruction framework for 3D real-time cine cardiovascular magnetic resonance (CMR) from highly undersampled data without requiring fully sampled training data. Methods: We developed a multi-dynamic low-rank deep image prior (ML-DIP) framework that models spatial image content and temporal deformation fields using separate neural networks. These networks are optimized per scan to reconstruct the dynamic image series directly from undersampled k-space data. ML-DIP was evaluated on (i) a 3D cine digital phantom with simulated premature ventricular contractions (PVCs), (ii) ten healthy subjects (including two scanned during both rest and exercise), and (iii) five patients with PVCs. Phantom results were assessed using peak signal-to-noise ratio (PSNR) and structural similarity index measure (SSIM). In vivo performance was evaluated by comparing left-ventricular function quantification (against 2D real-time cine) and image quality (against 2D real-time cine and binning-based 5D-Cine). Results: In the phantom study, ML-DIP achieved PSNR > 29 dB and SSIM > 0.90 for scan times as short as two minutes, while recovering cardiac motion, respiratory motion, and PVC events. In healthy subjects, ML-DIP yielded functional measurements comparable to 2D cine and higher image quality than 5D-Cine, including during exercise with high heart rates and bulk motion. In PVC patients, ML-DIP preserved beat-to-beat variability and reconstructed irregular beats, whereas 5D-Cine showed motion artifacts and information loss due to binning. Conclusion: ML-DIP enables high-quality 3D real-time CMR with acceleration factors exceeding 1,000 by learning low-rank spatial and temporal representations from undersampled data, without relying on external fully sampled training datasets.