Multimodal image fusion aims to integrate information from different imaging techniques to produce a comprehensive, detail-rich single image for downstream vision tasks. Existing methods based on local convolutional neural networks (CNNs) struggle to capture global features efficiently, while Transformer-based models are computationally expensive, although they excel at global modeling. Mamba addresses these limitations by leveraging selective structured state space models (S4) to effectively handle long-range dependencies while maintaining linear complexity. In this paper, we propose FusionMamba, a novel dynamic feature enhancement framework that aims to overcome the challenges faced by CNNs and Vision Transformers (ViTs) in computer vision tasks. The framework improves the visual state-space model Mamba by integrating dynamic convolution and channel attention mechanisms, which not only retains its powerful global feature modeling capability, but also greatly reduces redundancy and enhances the expressiveness of local features. In addition, we have developed a new module called the dynamic feature fusion module (DFFM). It combines the dynamic feature enhancement module (DFEM) for texture enhancement and disparity perception with the cross-modal fusion Mamba module (CMFM), which focuses on enhancing the inter-modal correlation while suppressing redundant information. Experiments show that FusionMamba achieves state-of-the-art performance in a variety of multimodal image fusion tasks as well as downstream experiments, demonstrating its broad applicability and superiority.
Multi-modal image analysis using deep learning (DL) lays the foundation for neoadjuvant treatment (NAT) response monitoring. However, existing methods prioritize extracting multi-modal features to enhance predictive performance, with limited consideration on real-world clinical applicability, particularly in longitudinal NAT scenarios with multi-modal data. Here, we propose the Multi-modal Response Prediction (MRP) system, designed to mimic real-world physician assessments of NAT responses in breast cancer. To enhance feasibility, MRP integrates cross-modal knowledge mining and temporal information embedding strategy to handle missing modalities and remain less affected by different NAT settings. We validated MRP through multi-center studies and multinational reader studies. MRP exhibited comparable robustness to breast radiologists, outperforming humans in predicting pathological complete response in the Pre-NAT phase (ΔAUROC 14% and 10% on in-house and external datasets, respectively). Furthermore, we assessed MRP’s clinical utility impact on treatment decision-making. MRP may have profound implications for enrolment into NAT trials and determining surgery extensiveness.
Accurately determining the molecular subtypes of breast cancer is important for the prognosis of breast cancer patients and can guide treatment selection. In this study, we develop a deep learning-based model for predicting the molecular subtypes of breast cancer directly from the diagnostic mammography and ultrasound images. Multi-modal deep learning with intra- and inter-modality attention modules (MDL-IIA) is proposed to extract important relations between mammography and ultrasound for this task. MDL-IIA leads to the best diagnostic performance compared to other cohort models in predicting 4-category molecular subtypes with Matthews correlation coefficient (MCC) of 0.837 (95% confidence interval [CI]: 0.803, 0.870). The MDL-IIA model can also discriminate between Luminal and Non-Luminal disease with an area under the receiver operating characteristic curve of 0.929 (95% CI: 0.903, 0.951). These results significantly outperform clinicians’ predictions based on radiographic imaging. Beyond molecular-level test, based on gene-level ground truth, our method can bypass the inherent uncertainty from immunohistochemistry test. This work thus provides a noninvasive method to predict the molecular subtypes of breast cancer, potentially guiding treatment selection for breast cancer patients and providing decision support for clinicians.
In this paper, we investigate an automated pipeline to estimate respiration signals from videos for premature infants in neonatal intensive care units (NICUs). Two flow estimation methods, namely the conventional optical flow- and deep learning-based flow estimation methods, were employed and compared to estimate pixel motion vectors between adjacent video frames. The respiratory signal is further extracted via motion factorization. The proposed methods were evaluated by comparing our automated extracted respiration signals to that extracted from chest impedance on videos of five premature infants. The overall average cross-correlation coefficients are 0.70 for the optical flow-based method and 0.74 for the deep flow-based method. The average root mean-squared errors are 6.10 and 4.55 for the optical flow- and the deep flow-based methods, respectively. The experimental results are promising for further investigation and clinical application of the video-based respiration monitoring method for infants in NICUs.