Segmentation of target volumes and organs at risk on computed tomography (CT) images constitutes an important step in the radiotherapy workflow. Artificial intelligence-based methods have significantly improved organ segmentation in medical images. Automatic segmentations are frequently evaluated using geometric metrics. Before a clinical implementation in the radiotherapy workflow, automatic segmentations must also be evaluated by clinicians. The aim of this study was to investigate the correlation between geometric metrics used for segmentation evaluation and the assessment performed by clinicians. In this study, we used the U-Net model to segment the liver in CT images from a publicly available dataset. The model's performance was evaluated using two geometric metrics: the Dice similarity coefficient and the Hausdorff distance. Additionally, a qualitative evaluation was performed by clinicians who reviewed the automatic segmentations to rate their clinical acceptability for use in the radiotherapy workflow. The correlation between the geometric metrics and the clinicians' evaluations was studied. The results showed that while the Dice coefficient and Hausdorff distance are reliable indicators of segmentation accuracy, they do not always align with clinician segmentation. In some cases, segmentations with high Dice scores still required clinician corrections before clinical use in the radiotherapy workflow. This study highlights the need for more comprehensive evaluation metrics beyond geometric measures to assess the clinical acceptability of artificial intelligence-based segmentation. Although the deep learning model provided promising segmentation results, the present study shows that standardized validation methodologies are crucial for ensuring the clinical viability of automatic segmentation systems.

Early identification of unresectable hepatocellular carcinoma (HCC) patients who may benefit from immune checkpoint inhibitors (ICIs) is crucial for optimizing outcomes. Here, we developed a multimodal fusion (MMF) system integrating CT-derived deep learning features and clinical data to predict overall survival (OS) and progression-free survival (PFS). Using retrospective multicenter data (n = 859), the MMF combining an ensemble deep learning (Ensemble-DL) model with clinical variables achieved strong external validation performance (C-index: OS = 0.74, PFS = 0.69), outperforming radiomics (29.8% OS improvement), mRECIST (27.6% OS improvement), clinical benchmarks (C-index: OS = 0.67, p = 0.0011; PFS = 0.65, p = 0.033), and Ensemble-DL (C-index: OS = 0.69, p = 0.0028; PFS = 0.66, p = 0.044). The MMF system effectively stratified patients across clinical subgroups and demonstrated interpretability through activation maps and radiomic correlations. Differential gene expression analysis revealed enrichment of the PI3K/Akt pathway in patients identified by the MMF system. The MMF system provides an interpretable, clinically applicable approach to guide personalized ICI treatment in unresectable HCC.

To assess the effects of industry-developed deep learning reconstruction with super resolution (DLR-SR) on single-shot turbo spin-echo (SshTSE) images with thickness of 2 mm with DLR (SshTSE^2mm) relative to those of images with a thickness of 5 mm with DLR (SSshTSE^5mm) in the patients with pancreatic cystic lesions. Thirty consecutive patients who underwent abdominal MRI examinations because of pancreatic cystic lesions under observation between June 2024 and July 2024 were enrolled. We qualitatively and quantitatively evaluated the image qualities of SshTSE^2mm and SshTSE^5mm with and without DLR-SR. The SNRs of the pancreas, spleen, paraspinal muscle, peripancreatic fat, and pancreatic cystic lesions of SshTSE^2mm with and without DLR-SR did not decrease in compared to that of SshTSE^5mm with and without DLR-SR. There were no significant differences in contrast-to-noise ratios (CNRs) of the pancreas-to-cystic lesions and fat between 4 types of images. SshTSE^2mm with DLR-SR had the highest image quality related to pancreas edge sharpness, perceived coarseness pancreatic duct clarity, noise, artifacts, overall image quality, and diagnostic confidence of cystic lesions, followed by SshTSE^2mm without DLR-SR and SshTSE^5mm with and without DLR-SR (P  <  0.0001). SshTSE^2mm with DLR-SR images had better quality than the other images and did not have decreased SNRs and CNRs. The thin-slice SshTSE with DLR-SR may be feasible and clinically useful for the evaluation of patients with pancreatic cystic lesions.

We explore biases present in publicly available fetal ultrasound (US) imaging datasets, currently at the disposal of researchers to train deep learning (DL) algorithms for prenatal diagnostics. As DL increasingly permeates the field of medical imaging, the urgency to critically evaluate the fairness of benchmark public datasets used to train them grows. Our thorough investigation reveals a multifaceted bias problem, encompassing issues such as lack of demographic representativeness, limited diversity in clinical conditions depicted, and variability in US technology used across datasets. We argue that these biases may significantly influence DL model performance, which may lead to inequities in healthcare outcomes. To address these challenges, we recommend a multilayered approach. This includes promoting practices that ensure data inclusivity, such as diversifying data sources and populations, and refining model strategies to better account for population variances. These steps will enhance the trustworthiness of DL algorithms in fetal US analysis.

Differences in CT-based body composition (BC) have been observed by race. We sought to investigate whether indices reporting census block group-level disadvantage, area deprivation index (ADI) and social vulnerability index (SVI), age, sex, and/or clinical factors could explain race-based differences in body composition. The first abdominal CT exams for patients in Durham County at a single institution in 2020 were analyzed using a fully automated and open-source deep learning BC analysis workflow to generate cross-sectional areas for skeletal muscle (SMA), subcutaneous fat (SFA), and visceral fat (VFA). Patient level demographic and clinical data were gathered from the electronic health record. State ADI ranking and SVI values were linked to each patient. Univariable and multivariable models were created to assess the association of demographics, ADI, SVI, and other relevant clinical factors with SMA, SFA, and VFA. 5,311 patients (mean age, 57.4 years; 55.5% female, 46.5% Black; 39.5% White 10.3% Hispanic) were included. At univariable analysis, race, ADI, SVI, sex, BMI, weight, and height were significantly associated with all body compartments (SMA, SFA, and VFA, all p<0.05). At multivariable analyses adjusted for patient characteristics and clinical comorbidities, race remained a significant predictor, whereas ADI did not. SVI was significant in a multivariable model with SMA.

Uterine sarcoma is a rare disease whose association with body composition parameters is poorly understood. This study explored the impact of body composition parameters on overall survival with uterine sarcoma. This multicenter study included 52 patients with uterine sarcomas treated at three Japanese hospitals between 2007 and 2023. A semi-automatic segmentation program based on deep learning analyzed transaxial CT images at the L3 vertebral level, calculating body composition parameters as follows: area indices (areas divided by height squared) of skeletal muscle, visceral and subcutaneous adipose tissue (SMI, VATI, and SATI, respectively); skeletal muscle density; and the visceral-to-subcutaneous fat area ratio (VSR). The optimal cutoff values for each parameter were calculated using maximally selected rank statistics with several p value approximations. The effects of body composition parameters and clinical data on overall survival (OS) and cancer-specific survival (CSS) were analyzed. Univariate Cox proportional hazards regression analysis revealed that advanced stage (III-IV) and high VSR were unfavorable prognostic factors for both OS and CSS. Multivariate Cox proportional hazard regression analysis revealed that advanced stage (III-IV) (hazard ratios (HRs), 4.67 for OS and 4.36 for CSS, p < 0.01), and high VSR (HRs, 9.36 for OS and 8.22 for CSS, p < 0.001) were poor prognostic factors for both OS and CSS. Added values were observed when the VSR was incorporated into the OS and the CSS prediction models. Increased VSR and tumor stage are significant predictors of poor overall survival in patients with uterine sarcoma.

This study aimed to evaluate radiomic models' ability to predict hypoxia-related biomarker expression in clear cell renal cell carcinoma (ccRCC). Clinical and molecular data from 190 patients were extracted from The Cancer Genome Atlas-Kidney Renal Clear Cell Carcinoma dataset, and corresponding CT imaging data were manually segmented from The Cancer Imaging Archive. A panel of 2,824 radiomic features was analyzed, and robust, high-interscanner-reproducibility features were selected. Gene expression data for 13 hypoxia-related biomarkers were stratified by tumor grade (1/2 vs. 3/4) and stage (I/II vs. III/IV) and analyzed using Wilcoxon rank sum test. Machine learning modeling was conducted using the High-Performance Random Forest (RF) procedure in SAS Enterprise Miner 15.1, with significance at P < 0.05. Descriptive univariate analysis revealed significantly lower expression of several biomarkers in high-grade and late-stage tumors, with KLF6 showing the most notable decrease. The RF model effectively predicted the expression of KLF6, ETS1, and BCL2, as well as PLOD2 and PPARGC1A underexpression. Stratified performance assessment showed improved predictive ability for RORA, BCL2, and KLF6 in high-grade tumors and for ETS1 across grades, with no significant performance difference across grade or stage. The RF model demonstrated modest but significant associations between texture metrics derived from clinical CT scans, such as GLDM and GLCM, and key hypoxia-related biomarkers including KLF6, BCL2, ETS1, and PLOD2. These findings suggest that radiomic analysis could support ccRCC risk stratification and personalized treatment planning by providing non-invasive insights into tumor biology.

Benign lymph node enlargement can mislead surgeons into overstaging colorectal cancer (CRC), causing unnecessarily extended lymphadenectomy. This study aimed to develop and validate a machine learning (ML) classifier utilizing multi-phase CT (MPCT) radiomics for accurate evaluation of the pre-treatment status of enlarged tumor-draining lymph nodes (TDLNs; defined as long-axis diameter ≥ 10 mm). This study included 430 pathologically confirmed CRC patients who underwent radical resection, stratified into a development cohort (n = 319; January 2015-December 2019, retrospectively enrolled) and test cohort (n = 111; January 2020-May 2023, prospectively enrolled). Radiomics features were extracted from multi-regional lesions (tumor and enlarged TDLNs) on MPCT. Following rigorous feature selection, optimal features were employed to train multiple ML classifiers. The top-performing classifier based on area under receiver operating characteristic curves (AUROCs) was validated. Ultimately, 15 classifiers based on features from multi-regional lesions were constructed (Tumor_{N, A}, _V; Ln_N, _A, _V; Ln, lymph node; _N, non-contrast phase; _A, arterial phase; _V, venous phase). Among all classifiers, the enlarged TDLNs fusion MPCT classifier (Ln_NAV) demonstrated the highest predictive efficacy, with AUROCs and AUPRCs of 0.820 and 0.883, respectively. When pre-treatment clinical variables were integrated (Clinical_Ln_NAV), the model's efficacy improved, with AUROCs of 0.839, AUPRCs of 0.903, accuracy of 76.6%, sensitivity of 67.7%, and specificity of 89.1%. The classifier Clinical_Ln_NAV demonstrated well performance in evaluating pre-treatment status of enlarged TDLNs. This tool may support clinicians in developing individualized treatment plans for CRC patients, helping to avoid inappropriate treatment. Question There are currently no effective non-invasive tools to assess the status of enlarged tumor-draining lymph nodes in colorectal cancer prior to treatment. Findings Pre-treatment multi-phase CT radiomics, combined with clinical variables, effectively assessed the status of enlarged tumor-draining lymph nodes, achieving a specificity of 89.1%. Clinical relevance statement The multi-phase CT-based classifier may assist clinicians in developing individualized treatment plans for colorectal cancer patients, potentially helping to avoid inappropriate preoperative adjuvant therapy and unnecessary extended lymphadenectomy.

Appropriate categorization based on magnetic resonance imaging (MRI) findings is important for managing intraductal papillary mucinous neoplasms (IPMNs). In this study, a large language model (LLM) that classifies IPMNs based on MRI findings was developed, and its performance was compared with that of less experienced human readers. The medical image management and processing systems of our hospital were searched to identify MRI reports of branch-duct IPMNs (BD-IPMNs). They were assigned to the training, validation, and testing datasets in chronological order. The model was trained on the training dataset, and the best-performing model on the validation dataset was evaluated on the test dataset. Furthermore, two radiology residents (Readers 1 and 2) and an intern (Reader 3) manually sorted the reports in the test dataset. The accuracy, sensitivity, and time required for categorizing were compared between the model and readers. The accuracy of the fine-tuned LLM for the test dataset was 0.966, which was comparable to that of Readers 1 and 2 (0.931-0.972) and significantly better than that of Reader 3 (0.907). The fine-tuned LLM had an area under the receiver operating characteristic curve of 0.982 for the classification of cyst diameter ≥ 10 mm, which was significantly superior to that of Reader 3 (0.944). Furthermore, the fine-tuned LLM (25 s) completed the test dataset faster than the readers (1,887-2,646 s). The fine-tuned LLM classified BD-IPMNs based on MRI findings with comparable performance to that of radiology residents and significantly reduced the time required.

Renal cell carcinoma (RCC) represents the most prevalent malignant neoplasm of the kidney, with a rising global incidence. Tumor nuclear grade is a crucial prognostic factor, guiding treatment decisions, but current histopathological grading via biopsy is invasive and prone to sampling errors. This study aims to assess the diagnostic performance and quality of CT-based radiomics for preoperatively predicting RCC nuclear grade. A comprehensive search was conducted across PubMed, Scopus, Embase, and Web of Science to identify relevant studies up until 19 April 2025. Quality was assessed using the QUADAS-2 and METRICS tools. A bivariate random-effects meta-analysis was performed to evaluate model performance, including sensitivity, specificity, and Area Under the Curve (AUC). Results from separate validation cohorts were pooled, and clinical and combined models were analyzed separately in distinct analyses. A total of 26 studies comprising 1993 individuals in 10 external and 16 internal validation cohorts were included. Meta-analysis of radiomics models showed pooled AUC of 0.88, sensitivity of 0.78, and specificity of 0.82. Clinical and combined (clinical-radiomics) models showed AUCs of 0.73 and 0.86, respectively. QUADAS-2 revealed significant risk of bias in the Index Test and Flow and Timing domains. METRICS scores ranged from 49.7 to 88.4%, with an average of 66.65%, indicating overall good quality, though gaps in some aspects of study methodologies were identified. This study suggests that radiomics models show great potential and diagnostic accuracy for non-invasive preoperative nuclear grading of RCC. However, challenges related to generalizability and clinical applicability remain, as further research with standardized methodologies, external validation, and larger cohorts is needed to enhance their reliability and integration into routine clinical practice.