While Multi-Task Learning (MTL) offers inherent advantages in complex domains such as medical imaging by enabling shared representation learning, effectively balancing task contributions remains a significant challenge. This paper addresses this critical issue by introducing DeepChest, a novel, computationally efficient and effective dynamic task-weighting framework specifically designed for multi-label chest X-ray (CXR) classification. Unlike existing heuristic or gradient-based methods that often incur substantial overhead, DeepChest leverages a performance-driven weighting mechanism based on effective analysis of task-specific loss trends. Given a network architecture (e.g., ResNet18), our model-agnostic approach adaptively adjusts task importance without requiring gradient access, thereby significantly reducing memory usage and achieving a threefold increase in training speed. It can be easily applied to improve various state-of-the-art methods. Extensive experiments on a large-scale CXR dataset demonstrate that DeepChest not only outperforms state-of-the-art MTL methods by 7% in overall accuracy but also yields substantial reductions in individual task losses, indicating improved generalization and effective mitigation of negative transfer. The efficiency and performance gains of DeepChest pave the way for more practical and robust deployment of deep learning in critical medical diagnostic applications. The code is publicly available at https://github.com/youssefkhalil320/DeepChest-MTL

Chronic thromboembolic pulmonary hypertension (CTEPH) is a potentially life-threatening condition, classified as group 4 pulmonary hypertension (PH), caused by stenosis or occlusion of the pulmonary arteries due to unresolved thromboembolic material. The prognosis for untreated CTEPH patients is poor because it leads to elevated pulmonary artery pressure and right heart failure. Early and accurate diagnosis of CTEPH is crucial because it remains the only form of PH that is potentially curable. However, diagnosing CTEPH is often challenging and frequently delayed or misdiagnosed. This review discusses the current role of multimodal imaging in diagnosing CTEPH, guiding clinical decision-making, and monitoring post-treatment outcomes. The characteristic findings, strengths, and limitations of various imaging modalities, such as computed tomography, ventilation-perfusion lung scintigraphy, digital subtraction pulmonary angiography, and magnetic resonance imaging, are evaluated. Additionally, the role of artificial intelligence in improving the diagnosis and treatment outcomes of CTEPH is explored. Optimal patient assessment and therapeutic decision-making should ideally be conducted in specialized centers by a multidisciplinary team, utilizing data from imaging, pulmonary hemodynamics, and patient comorbidities.

Due to imbalanced data values and high-dimensional features of lung cancer from CT scans images creates significant challenges in clinical research. The improper classification of these images leads towards higher complexity in classification process. These critical issues compromise the extraction of biomedical traits and also design incomplete classification of lung cancer. As the conventional approaches are partially successful in dealing with the complex nature of high-dimensional and imbalanced biomedical data for lung cancer classification. Thus, there is a crucial need to develop a robust classification technique which can address these major concerns in the classification of lung cancer images. In this paper, we propose a novel structural formation of the oblique decision tree (OBT) using a swarm intelligence technique, namely, the Binary Bat Swarm Algorithm (BBSA). The application of BBSA enables a competitive recognition rate to make structural reforms while building OBT. Such integration improves the ability of the machine learning swarm classifier (MLSC) to handle high-dimensional features and imbalanced biomedical datasets. The adaptive feature selection using BBSA allows for the exploration and selection of relevant features required for classification from ODT. The ODT classifier introduces flexibility in decision boundaries, which enables it to capture complex linkages between biomedical data. The proposed MLSC model effectively handles high-dimensional, imbalanced lung cancer datasets using TCGA_LUSC_2016 and TCGA_LUAD_2016 modalities, achieving superior precision, recall, F-measure, and execution efficiency. The experiments are conducted in Python to evaluate the performance metrics that consistently demonstrate enhanced classification accuracy and reduced misclassification rates compared to existing methods. The MLSC is assessed in terms of both qualitative and quantitative measurements to study the capability of the proposed MLSC in classifying the instances more effectively than the conventional state-of-the-art methods.

Lung cancer is the leading cause of cancer mortality worldwide, and non-invasive methods for detecting key mutations and staging are essential for improving patient outcomes. Here, we compare the performance of two machine learning models - FMCIB+XGBoost, a supervised model with domain-specific pretraining, and Dinov2+ABMIL, a self-supervised model with attention-based multiple-instance learning - on 3D lung nodule data from the Stanford Radiogenomics and Lung-CT-PT-Dx cohorts. In the task of KRAS and EGFR mutation detection, FMCIB+XGBoost consistently outperformed Dinov2+ABMIL, achieving accuracies of 0.846 and 0.883 for KRAS and EGFR mutations, respectively. In cancer staging, Dinov2+ABMIL demonstrated competitive generalization, achieving an accuracy of 0.797 for T-stage prediction in the Lung-CT-PT-Dx cohort, suggesting SSL's adaptability across diverse datasets. Our results emphasize the clinical utility of supervised models in mutation detection and highlight the potential of SSL to improve staging generalization, while identifying areas for enhancement in mutation sensitivity.

<i>"Just Accepted" papers have undergone full peer review and have been accepted for publication in <i>Radiology: Artificial Intelligence</i>. This article will undergo copyediting, layout, and proof review before it is published in its final version. Please note that during production of the final copyedited article, errors may be discovered which could affect the content.</i> Purpose To estimate the total lung volume (TLV) from real and synthetic frontal chest radiographs (CXR) on a pixel level using lung thickness maps generated by a U-Net deep learning model. Materials and Methods This retrospective study included 5,959 chest CT scans from two public datasets: the lung nodule analysis 2016 (<i>n</i> = 656) and the Radiological Society of North America (RSNA) pulmonary embolism detection challenge 2020 (<i>n</i> = 5,303). Additionally, 72 participants were selected from the Klinikum Rechts der Isar dataset (October 2018 to December 2019), each with a corresponding chest radiograph taken within seven days. Synthetic radiographs and lung thickness maps were generated using forward projection of CT scans and their lung segmentations. A U-Net model was trained on synthetic radiographs to predict lung thickness maps and estimate TLV. Model performance was assessed using mean squared error (MSE), Pearson correlation coefficient <b>(r)</b>, and two-sided Student's t-distribution. Results The study included 72 participants (45 male, 27 female, 33 healthy: mean age 62 years [range 34-80]; 39 with chronic obstructive pulmonary disease: mean age 69 years [range 47-91]). TLV predictions showed low error rates (MSEPublic-Synthetic = 0.16 L², MSEKRI-Synthetic = 0.20 L², MSEKRI-Real = 0.35 L²) and strong correlations with CT-derived reference standard TLV (nPublic-Synthetic = 1,191, r = 0.99, <i>P</i> < .001; nKRI-Synthetic = 72, r = 0.97, <i>P</i> < .001; nKRI-Real = 72, r = 0.91, <i>P</i> < .001). When evaluated on different datasets, the U-Net model achieved the highest performance for TLV estimation on the Luna16 test dataset, with the lowest mean squared error (MSE = 0.09 L²) and strongest correlation (<i>r</i> = 0.99, <i>P</i> <.001) compared with CT-derived TLV. Conclusion The U-Net-generated pixel-level lung thickness maps successfully estimated TLV for both synthetic and real radiographs. ©RSNA, 2025.

This work aimed to develop an automated method for quantifying the distribution and severity of perfusion changes on CT pulmonary angiography (CTPA) in patients with chronic thromboembolic pulmonary hypertension (CTEPH) and to assess their associations with clinical parameters and expert annotations. Following automated segmentation of the chest, a machine-learning model assuming three distributions of attenuation in the pulmonary parenchyma (hyperemic, normal, and oligemic) was fitted to the attenuation histogram of CTPA images using Bayesian analysis. The proportion of each component, its spatial heterogeneity (entropy), and center-to-periphery distribution of the attenuation were calculated and correlated with the findings on CTPA semi-quantitatively evaluated by radiologists and with clinical function tests. CTPA scans from 52 patients (mean age, 65.2 ± 13.0 years; 27 men) diagnosed with CTEPH were analyzed. An inverse correlation was observed between the proportion of normal parenchyma and brain natriuretic propeptide (proBNP, ρ = -0.485, p = 0.001), mean pulmonary arterial pressure (ρ = -0.417, p = 0.002) and pulmonary vascular resistance (ρ = -0.556, p < 0.0001), mosaic attenuation (ρ = -0.527, p < 0.0001), perfusion centralization (ρ = -0.489, p = < 0.0001), and right ventricular diameter (ρ = -0.451, p = 0.001). The entropy of hyperemic parenchyma showed a positive correlation with the pulmonary wedge pressure (ρ = 0.402, p = 0.003). The slope of center-to-periphery attenuation distribution correlated with centralization (ρ = -0.477, p < 0.0001), and with proBNP (ρ = -0.463, p = 0.002). This study validates an automated system that leverages Bayesian analysis to quantify the severity and distribution of perfusion changes in CTPA. The results show the potential of this method to support clinical evaluations of CTEPH by providing reproducible and objective measures. Question This study introduces an automated method for quantifying the extent and spatial distribution of pulmonary perfusion abnormalities in CTEPH using variational Bayesian estimation. Findings Quantitative measures describing the extent, heterogeneity, and distribution of perfusion changes demonstrate strong correlations with key clinical hemodynamic indicators. Clinical relevance The automated quantification of perfusion changes aligns closely with radiologists' evaluations, delivering a standardized, reproducible measure with clinical relevance.

To assess the predictive performance, risk stratification capabilities, and auxiliary diagnostic utility of radiomics, deep learning, and fusion models in identifying visceral pleural invasion (VPI) in lung adenocarcinoma. A total of 449 patients (female:male, 263:186; 59.8 ± 10.5 years) diagnosed with clinical IA stage lung adenocarcinoma (LAC) from two distinct hospitals were enrolled in the study and divided into a training cohort (n = 289) and an external test cohort (n = 160). The fusion models were constructed from the feature level and the decision level respectively. A comprehensive analysis was conducted to assess the prediction ability and prognostic value of radiomics, deep learning, and fusion models. The diagnostic performance of radiologists of varying seniority with and without the assistance of the optimal model was compared. The late fusion model demonstrated superior diagnostic performance (AUC = 0.812) compared to clinical (AUC = 0.650), radiomics (AUC = 0.710), deep learning (AUC = 0.770), and the early fusion models (AUC = 0.586) in the external test cohort. The multivariate Cox regression analysis showed that the VPI status predicted by the late fusion model were independently associated with patient disease-free survival (DFS) (p = 0.044). Furthermore, model assistance significantly improved radiologist performance, particularly for junior radiologists; the AUC increased by 0.133 (p < 0.001) reaching levels comparable to the senior radiologist without model assistance (AUC: 0.745 vs. 0.730, p = 0.790). The proposed decision-level (late fusion) model significantly reducing the risk of overfitting and demonstrating excellent robustness in multicenter external validation, which can predict VPI status in LAC, aid in prognostic stratification, and assist radiologists in achieving higher diagnostic performance.

Recent advancements in multimodal Large Language Models (LLMs) have significantly enhanced the automation of medical image analysis, particularly in generating radiology reports from chest X-rays (CXR). However, these models still suffer from hallucinations and clinically significant errors, limiting their reliability in real-world applications. In this study, we propose Look & Mark (L&M), a novel grounding fixation strategy that integrates radiologist eye fixations (Look) and bounding box annotations (Mark) into the LLM prompting framework. Unlike conventional fine-tuning, L&M leverages in-context learning to achieve substantial performance gains without retraining. When evaluated across multiple domain-specific and general-purpose models, L&M demonstrates significant gains, including a 1.2% improvement in overall metrics (A.AVG) for CXR-LLaVA compared to baseline prompting and a remarkable 9.2% boost for LLaVA-Med. General-purpose models also benefit from L&M combined with in-context learning, with LLaVA-OV achieving an 87.3% clinical average performance (C.AVG)-the highest among all models, even surpassing those explicitly trained for CXR report generation. Expert evaluations further confirm that L&M reduces clinically significant errors (by 0.43 average errors per report), such as false predictions and omissions, enhancing both accuracy and reliability. These findings highlight L&M's potential as a scalable and efficient solution for AI-assisted radiology, paving the way for improved diagnostic workflows in low-resource clinical settings.

In this work, we investigate the performance across multiple classification models to classify chest X-ray images into four categories of COVID-19, pneumonia, tuberculosis (TB), and normal cases. We leveraged transfer learning techniques with state-of-the-art pre-trained Convolutional Neural Networks (CNNs) models. We fine-tuned these pre-trained architectures on a labeled medical x-ray images. The initial results are promising with high accuracy and strong performance in key classification metrics such as precision, recall, and F1 score. We applied Gradient-weighted Class Activation Mapping (Grad-CAM) for model interpretability to provide visual explanations for classification decisions, improving trust and transparency in clinical applications.

Recent vision-language foundation models deliver state-of-the-art results on natural image classification but falter on medical images due to pronounced domain shifts. At the same time, training a medical foundation model requires substantial resources, including extensive annotated data and high computational capacity. To bridge this gap with minimal overhead, we introduce MedBridge, a lightweight multimodal adaptation framework that re-purposes pretrained VLMs for accurate medical image diagnosis. MedBridge comprises three key components. First, a Focal Sampling module that extracts high-resolution local regions to capture subtle pathological features and compensate for the limited input resolution of general-purpose VLMs. Second, a Query Encoder (QEncoder) injects a small set of learnable queries that attend to the frozen feature maps of VLM, aligning them with medical semantics without retraining the entire backbone. Third, a Mixture of Experts mechanism, driven by learnable queries, harnesses the complementary strength of diverse VLMs to maximize diagnostic performance. We evaluate MedBridge on five medical imaging benchmarks across three key adaptation tasks, demonstrating its superior performance in both cross-domain and in-domain adaptation settings, even under varying levels of training data availability. Notably, MedBridge achieved over 6-15% improvement in AUC compared to state-of-the-art VLM adaptation methods in multi-label thoracic disease diagnosis, underscoring its effectiveness in leveraging foundation models for accurate and data-efficient medical diagnosis. Our code is available at https://github.com/ai-med/MedBridge.