This study aims to construct a survival prognosis prediction model for muscle-invasive bladder cancer based on CT imaging features. A total of 91 patients with muscle-invasive bladder cancer were sourced from the TCGA and TCIA dataset and were divided into a training group (64 cases) and a validation group (27 cases). Additionally, 54 patients with muscle-invasive bladder cancer were retrospectively collected from our hospital to serve as an external test group; their enhanced CT imaging data were analyzed and processed to identify the most relevant radiomic features. Five distinct machine learning methods were employed to develop the optimal radiomics model, which was then combined with clinical data to create a nomogram model aimed at accurately predicting the overall survival (OS) of patients with muscle-invasive bladder cancer. The model's performance was ultimately assessed using various evaluation methods, including the ROC curve, calibration curve, decision curve, and Kaplan-Meier (KM) analysis. Eight radiomic features were identified for modeling analysis. Among the models evaluated, the Gradient Boosting Machine (GBM) In the prediction of OS performed the best. the 2-year AUCs were 0.859, 95% CI (0.767-0.952) for the training group, 0.850, 95% CI (0.705-0.995) for the validation group, and 0.700, 95% CI (0.520-0.880) for the external test group. The 3-year AUCs were 0.809, 95% CI (0.704-0.913) for the training group, 0.895, 95% CI (0.768-1.000) for the validation group, and 0.730, 95% CI (0.569-0.891) for the external test group. The nomogram model incorporating clinical data achieved superior results, the AUCs for predicting 2-year OS were 0.913 (95% CI: 0.83-0.98) for the training group, 0.86 (95% CI: 0.78-0.96) for the validation group, and 0.778 (95% CI: 0.69-0.94) for the external test group; for predicting 3-year OS, the AUCs were 0.837 (95% CI: 0.83-0.98) for the training group, 0.982 (95% CI: 0.84-1.0) for the validation group, and 0.785 (95% CI: 0.75-0.96) for the external test group. The calibration curve demonstrated excellent calibration of the model, while the decision curve and KM analysis indicated that the model possesses substantial clinical utility. The GBM model, based on the radiomic features of enhanced CT imaging, holds significant potential for predicting the prognosis of patients with muscle-invasive bladder cancer. Furthermore, the combined model, which incorporates clinical features, demonstrates enhanced performance and is beneficial for clinical decision-making.

To investigate a computed tomography (CT)-based multiparameter deep learning-radiomic model (DLRM) for predicting the preoperative tumor budding (TB) grade in patients with rectal cancer. Data from 135 patients with histologically confirmed rectal cancer (85 in the Bd1+2 group and 50 in the Bd3 group) were retrospectively included. Deep learning (DL) features and hand-crafted radiomic (HCR) features were separately extracted and selected from preoperative CT-based extracellular volume (ECV) parameter images and venous-phase images. Six predictive signatures were subsequently constructed from machine learning classification algorithms. Finally, a combined DL and HCR model, the DLRM, was established to predict the TB grade of rectal cancer patients by merging the DL and HCR features from the two image sets. In the training and test cohorts, the AUC values of the DLRM were 0.976 [95% CI: 0.942-0.997] and 0.976 [95% CI: 0.942-1.00], respectively. The DLRM had good output agreement and clinical applicability according to calibration curve analysis and DCA, respectively. The DLRM outperformed the individual DL and HCR signatures in terms of predicting the TB grade of rectal cancer patients (p < 0.05). The DLRM can be used to evaluate the TB grade of rectal cancer patients in a noninvasive manner before surgery, thereby providing support for clinical treatment decision-making for these patients.

Prostate cancer (PCa) is the second most common cancer in men and has a significant health and social burden, necessitating advances in early detection, prognosis, and treatment strategies. Improvement in medical imaging has significantly impacted early PCa detection, characterization, and treatment planning. However, with an increasing number of patients with PCa and comparatively fewer PCa imaging experts, interpreting large numbers of imaging data is burdensome, time-consuming, and prone to variability among experts. With the revolutionary advances of artificial intelligence (AI) in medical imaging, image interpretation tasks are becoming easier and exhibit the potential to reduce the workload on physicians. Generative AI (GenAI) is a recently popular sub-domain of AI that creates new data instances, often to resemble patterns and characteristics of the real data. This new field of AI has shown significant potential for generating synthetic medical images with diverse and clinically relevant information. In this narrative review, we discuss the basic concepts of GenAI and cover the recent application of GenAI in the PCa imaging domain. This review will help the readers understand where the PCa research community stands in terms of various medical image applications like generating multi-modal synthetic images, image quality improvement, PCa detection, classification, and digital pathology image generation. We also address the current safety concerns, limitations, and challenges of GenAI for technical and clinical adaptation, as well as the limitations of current literature, potential solutions, and future directions with GenAI for the PCa community.

To investigate the effect of accelerated deep-learning (DL) multi-b-value DWI (Mb-DWI) on acquisition time, image quality, and predictive ability of microvascular invasion (MVI) in BCLC stage A hepatocellular carcinoma (HCC), compared to standard Mb-DWI. Patients who underwent liver MRI were prospectively collected. Subjective image quality, signal-to-noise ratio (SNR), lesion contrast-to-noise ratio (CNR), and Mb-DWI-derived parameters from various models (mono-exponential model, intravoxel incoherent motion, diffusion kurtosis imaging, and stretched exponential model) were calculated and compared between the two sequences. The Mb-DWI parameters of two sequences were compared between MVI-positive and MVI-negative groups, respectively. ROC and logistic regression analysis were performed to evaluate and identify the predictive performance. The study included 118 patients. 48/118 (40.67%) lesions were identified as MVI positive. DL Mb-DWI significantly reduced acquisition time by 52.86%. DL Mb-DWI produced significantly higher overall image quality, SNR, and CNR than standard Mb-DWI. All diffusion-related parameters except pseudo-diffusion coefficient showed significant differences between the two sequences. Both in DL and standard Mb-DWI, the apparent diffusion coefficient, true diffusion coefficient (D), perfusion fraction (f), mean diffusivity (MD), mean kurtosis (MK), and distributed diffusion coefficient (DDC) values were significantly different between MVI-positive and MVI-negative groups. The combination of D, f, and MK yield the highest AUC of 0.912 and 0.928 in standard and DL sequences, with no significant difference regarding the predictive efficiency. The DL Mb-DWI significantly reduces acquisition time and improves image quality, with comparable predictive performance to standard Mb-DWI in discriminating MVI status in BCLC stage A HCC.

In pancreatic stereotactic body radiotherapy (SBRT), accurate motion management is crucial for the safe delivery of high doses per fraction. Intra-fraction tracking with magnetic resonance imaging-guidance for gated SBRT has shown potential for improved local control. Visualisation of pancreas (and surrounding organs) remains challenging in intra-fraction kilo-voltage (kV) imaging, requiring implanted fiducials. In this study, we investigate patient-specific deep-learning approaches to track the gross-tumour-volume (GTV), pancreas-head and the whole-pancreas in intra-fraction kV images. Conditional-generative-adversarial-networks were trained and tested on data from 25 patients enrolled in an ethics-approved pancreatic SBRT trial for contour prediction on intra-fraction 2D kV images. Labelled digitally-reconstructed-radiographs (DRRs) were generated from contoured planning-computed-tomography (CTs) (CT-DRRs) and cone-beam-CTs (CBCT-DRRs). A population model was trained using CT-DRRs of 19 patients. Two patient-specific model types were created for six additional patients by fine-tuning the population model using CBCT-DRRs (CBCT-models) or CT-DRRs (CT-models) acquired in exhale-breath-hold. Model predictions on unseen triggered-kV images from the corresponding six patients were evaluated against projected-contours using Dice-Similarity-Coefficient (DSC), centroid-error (CE), average Hausdorff-distance (AHD), and Hausdorff-distance at 95th-percentile (HD95). The mean ± 1SD (standard-deviation) DSCs were 0.86 ± 0.09 (CBCT-models) and 0.78 ± 0.12 (CT-models). For AHD and CE, the CBCT-model predicted contours within 2.0 mm ≥90.3 % of the time, while HD95 was within 5.0 mm ≥90.0 % of the time, and had a prediction time of 29.2 ± 3.7 ms per contour. The patient-specific CBCT-models outperformed the CT-models and predicted the three contours with 90th-percentile error ≤2.0 mm, indicating the potential for clinical real-time application.

This review explores the significant progress and applications of artificial intelligence (AI) in obstetrics and gynecological MRI, charting its development from foundational algorithmic techniques to deep learning strategies and advanced radiomics. This review features research published over the last few years that has used AI with MRI to identify specific conditions such as uterine leiomyosarcoma, endometrial cancer, cervical cancer, ovarian tumors, and placenta accreta. In addition, it covers studies on the application of AI for segmentation and quality improvement in obstetrics and gynecology MRI. The review also outlines the existing challenges and envisions future directions for AI research in this domain. The growing accessibility of extensive datasets across various institutions and the application of multiparametric MRI are significantly enhancing the accuracy and adaptability of AI. This progress has the potential to enable more accurate and efficient diagnosis, offering opportunities for personalized medicine in the field of obstetrics and gynecology.

More cases of thyroid micro-nodules have been diagnosed annually in recent years because of advancements in diagnostic technologies and increased public health awareness. To explore the application value of various machine learning (ML) algorithms based on dual-layer spectral computed tomography (DLCT) quantitative parameters in distinguishing benign from malignant thyroid micro-nodules. All 338 thyroid micro-nodules (177 malignant micro-nodules and 161 benign micro-nodules) were randomly divided into a training cohort (n = 237) and a testing cohort (n = 101) at a ratio of 7:3. Four typical radiological features and 19 DLCT quantitative parameters in the arterial phase and venous phase were measured. Recursive feature elimination was employed for variable selection. Three ML algorithms-support vector machine (SVM), logistic regression (LR), and naive Bayes (NB)-were implemented to construct predictive models. Predictive performance was evaluated via receiver operating characteristic (ROC) curve analysis. A variable set containing 6 key variables with "one standard error" rules was identified in the SVM model, which performed well in the training and testing cohorts (area under the ROC curve (AUC): 0.924 and 0.931, respectively). A variable set containing 2 key variables was identified in the NB model, which performed well in the training and testing cohorts (AUC: 0.882 and 0.899, respectively). A variable set containing 8 key variables was identified in the LR model, which performed well in the training and testing cohorts (AUC: 0.924 and 0.925, respectively). And nine ML models were developed with varying variable sets (2, 6, or 8 variables), all of which consistently achieved AUC values above 0.85 in the training, cross validation (CV)-Training, CV-Validation, and testing cohorts. Artificial intelligence-based DLCT quantitative parameters are promising for distinguishing benign from malignant thyroid micro-nodules.

Detecting liver tumors via computed tomography (CT) scans is a critical but labor-intensive task. Extensive expert annotations are needed to train effective machine learning models. This study presents an innovative approach that leverages federated learning in combination with a teacher‒student framework, an enhanced slice-aware network (SANet), and semisupervised learning (SSL) techniques to improve the CT-based liver tumor detection process while significantly reducing its labor and time costs. Federated learning enables collaborative model training to be performed across multiple institutions without sharing sensitive patient data, thus ensuring privacy and security. The teacher-student SANet framework takes advantage of both teacher and student models, with the teacher model providing reliable pseudolabels that guide the student model in a semisupervised manner. This method not only improves the accuracy of liver tumor detection but also reduces the dependence on extensively annotated datasets. The proposed method was validated through simulation experiments conducted in four scenarios, and it demonstrated a model accuracy of 83%, which represents an improvement over the original locally trained models. This study presents a promising method for enhancing the CT-based liver tumor detection while reducing the incurred labor and time costs by utilizing federated learning, the teacher-student SANet framework, and SSL techniques. Compared with previous approaches, the proposed method achieved a model accuracy of 83%, representing a significant improvement. Not applicable.

To improve the prediction of immune checkpoint inhibitors (ICIs) efficacy in hepatocellular carcinoma (HCC), this study categorized the tumor immune microenvironment (TIME) into two types: immune-activated (IA), characterized by a high CD8 + score and high PD-L1 combined positive score (CPS), and non-immune-activated (NIA), encompassing all other conditions. We aimed to develop an MRI-based radiomics model to predict TIME types and validate its predictive capability for ICIs efficacy in HCC patients receiving anti-PD-1/PD-L1 therapy. The study included 200 HCC patients who underwent preoperative/pretreatment multiparametric contrast-enhanced MRI (Cohort 1: 168 HCC patients with hepatectomy from two centres; Cohort 2: 42 advanced HCC patients on anti-PD-1/PD-L1 therapy). In Cohort 1, after feature selection, clinical, intratumoral radiomics, peritumoral radiomics, combined radiomics, and clinical-radiomics models were established using machine learning algorithms. In cohort 2, the clinical-radiomics model's predictive ability for ICIs efficacy was assessed. In Cohort 1, the AUC values for intratumoral, peritumoral, and combined radiomics models were 0.825, 0.809, and 0.868, respectively, in the internal validation set, and 0.73, 0.759, and 0.822 in the external validation set; the clinical-radiomics model incorporating neutrophil-to-lymphocyte ratio, tumor size, and combined radiomics score achieved an AUC of 0.887 in the internal validation set, outperforming clinical model (P = 0.049), and an AUC of 0.837 in the external validation set. In cohort 2, the clinical-radiomics model stratified patients into low- and high-score groups, demonstrating a significant difference in objective response rate (p = 0.003) and progression-free survival (p = 0.031). The clinical-radiomics model is effective in predicting TIME types and efficacy of ICIs in HCC, potentially aiding in treatment decision-making.