Computed tomography (CT) and biopsy may be insufficient for preoperative evaluation of the grade and outcome of patients with chondrosarcoma. The aim of this study was to develop and validate a CT-based deep learning radiomics model (DLRM) for predicting histologic grade and prognosis in chondrosarcoma (CS).
A multicenter 211 (training cohort/ test cohort, 127/84) CS patients were enrolled. Radiomics signature (RS), deep learning signature (DLS), and DLRM incorporating radiomics and deep learning features were developed for predicting the grade. Kaplan-Meier survival analysis was used to assess the association of the model-predicted grade with recurrence-free survival (RFS). Model performance was evaluated with the area under the receiver operating characteristic curve (AUC) and the Harrell’s concordance index (C-index).
The DLRM (AUC, 0.879; 95 % confidence interval [CI], 0.802–0.956) outperformed (z = 2.773, P=0.006) the RS (AUC, 0.715;95 % CI, 0.606–0.825) in predicting grade in the test cohort. RFS showed significant differences (log-rank test, P<0.05) between low-grade and high-grade patients stratified by DLRM. The DLRM achieved a higher C-index (0.805; 95 % CI, 0.694–0.916) than the RS (0.692, 95 % CI, 0.540–0.844) did in predicting RFS for CS patients in the test cohort.
The DLRM can accurately predict the histologic grade and prognosis in CS.
Intracranial aneurysms (IAs) pose a severe health risk due to the potential for subarachnoid hemorrhage upon rupture. This study aims to conduct a systematic review and meta-analysis on the accuracy of radiomics features derived from computed tomography angiography (CTA) in differentiating ruptured from unruptured IAs.
A systematic search was performed across multiple databases for articles published up to January 2024. Observational studies analyzing CTA using radiomics features were included. The area under the curve (AUC) for classifying ruptured vs. unruptured IAs was pooled using a random-effects model. Subgroup analyses were conducted based on the use of radiomics-only features versus radiomics plus additional image-based features, as well as the type of filters used for image processing.
Six studies with 4,408 patients were included. The overall pooled AUC for radiomics features in differentiating ruptured from unruptured IAs was 0.86 (95% CI: 0.84–0.88). The AUC was 0.85 (95% CI: 0.82–0.88) for studies using only radiomics features and 0.87 (95% CI: 0.83–0.91) for studies incorporating radiomics plus additional image-based features. Subgroup analysis based on filter type showed an AUC of 0.87 (95% CI: 0.83–0.90) for original filters and 0.86 (95% CI: 0.81–0.90) for studies using additional filters.
Radiomics-based models demonstrate very good diagnostic accuracy in classifying ruptured and unruptured IAs, with AUC values exceeding 0.8. This highlights the potential of radiomics as a useful tool in the non-invasive assessment of aneurysm rupture risk, particularly in the management of patients with multiple aneurysms.
The purpose of this monocentric retrospective study consisted in exploring the potential improvement of the assessment of renal masses on MRI by using the T1 (T1m) and T2 (T2m) mapping relaxation times.
We recorded the renal cortex values of 125 patients with normal kidneys (reference group) and 75 patients with renal masses on a clinical 3 T MR unit using T1m and T2m sequences.
For the quantitative evaluation, measurements were performed by delineating ROIs on T1m and T2m sequences in renal cortex of the reference group and in renal masses.
Interobserver agreement for the qualitative analysis of image quality was assessed using quadratic Cohen’s weighted kappa statistics (k).
Student’s paired t-test and non-parametric Kruskal-Wallis test were used to compare our datasets in terms of T1m and T2m values.
For the cohort of reference group, mean renal cortex T1m and T2m values were 1,529 ± 83 ms and 98 ± 7 ms, respectively. No statistically significant differences were found for T1m and T2m in the reference group regardless of age, gender or eGRF categories.
For the group with renal masses, mean T1m and T2m values were 1,667 ± 87 ms and 105 ± 8 ms; 1,621 ± 96 ms and 117 ± 6 ms, and 1,530 ± 62 ms and 85 ± 4 ms for renal cell carcinomas, angiomyolipomas, and oncocytomas, respectively. For T1m values, there was no significant difference (p = 0.37) among the three types of renal masses. Among histological subtypes we have found: RCC versus angiomyolipoma (p = 0.25), RCC versus oncocytoma (p = 0.15), and oncocytoma versus angiomyolipoma (p = 0.47).
However, we have found a statistically significant difference for the T2m value (p = 0.0005). Among histological subtypes, only T2m values were statistically significant for each combination: RCC versus angiomyolipoma (p = 0.012), RCC versus oncocytoma (p = 0.0002), and oncocytoma versus angiomyolipoma (p = 0.003).
As this is the largest normal patient cohort, the T1m and T2m values recorded could be proposed as reference values and can play a role in the differential diagnosis between benign and malignant renal tumoral masses.
The consensus on whether Transjugular intrahepatic portosystemic shunt (TIPS) should be combined with variceal embolization in the treatment of portal hypertension-induced bleeding has not yet been reached. This study aimed to compare the difference in rebleeding incidence between TIPS and TIPS combined with variceal embolization and to analyze the optimal population for variceal embolization.
Clinical data of 721 patients undergoing TIPS were retrospectively collected. Patients were divided into two groups: TIPS alone (n = 155) and TIPS with embolization (TIPS+E, n = 251). Kaplan-Meier (KM) curves were used to analyze prognostic differences between the two groups, and subgroup analysis was conducted based on post-TIPS portal pressure gradient (PPG) exceeding 12 mmHg.
After TIPS placement, the mean PPG significantly decreased for all patients. A total of 51 patients (12.6 %) experienced rebleeding, with 24 cases (15.9 %) in the TIPS group and 27 cases (10.6 %) in the TIPS+E group. There was no significant difference in cumulative rebleeding incidence between the TIPS+E and TIPS groups. In the subgroup with post-TIPS PPG greater than 12 mmHg, the cumulative rebleeding incidence was significantly lower in the TIPS+E group compared to the TIPS group (HR = 0.47, 95 %CI = 0.24–0.93, Log rank P = 0.026). No significant difference was found in patients with a post-TIPS PPG less than 12 mmHg.
For patients with post-TIPS PPG exceeding 12 mmHg, simultaneous variceal embolization with TIPS placement significantly reduces the risk of rebleeding.
The aim of this study was to develop a diagnostic model for predicting indolent lymphoma or aggressive lymphoma using clinical information and ultrasound characteristics of superficial lymph nodes.
Patients with confirmed pathological lymphoma subtypes who had undergone ultrasound and contrast-enhanced ultrasound examinations were enrolled. Clinical and ultrasound imaging features were retrospectively analysed and compared to the pathological results, which were considered the gold standard for diagnosis. Two diagnostic models were developed: a clinical model (Model-C) using clinical data only, and a combined model (Model-US) integrating ultrasound features into the clinical model. The efficacy of these models in differentiating between indolent and aggressive lymphoma was compared.
In total, 236 consecutive patients were enrolled, including 78 patients with indolent lymphomas and 158 patients with aggressive lymphomas. Receiver operating characteristic (ROC) curve analysis revealed that the areas under the curves of Model-C and Model-US were 0.78 (95 % confidence interval: 0.72–0.84) and 0.87 (95 % confidence interval: 0.82–0.92), respectively (p < 0.001). Model-US was further evaluated for calibration and is presented as a nomogram.
The diagnostic model incorporated clinical and ultrasound characteristics and offered a noninvasive method for assessing lymphoma with good discrimination and calibration.
To assess the feasibility of the single-shot turbo spin echo sequence using deep learning-based reconstruction (DLR) (HASTEDL) with enhanced denoising for pancreas MRI.
Patients who underwent pancreas MRI from March to April 2021 were included. Four T2-weighted images (non-FS conventional HASTE vs. HASTEDL with enhanced denoising and FS HASTEDL with enhanced denoising vs. HASTEDL) were acquired. Two readers independently assessed the image quality parameters of the two non-FS image sets using a 4-point Likert scale. The signal-to-noise ratio (SNR) of the cystic lesions and pancreatic parenchyma and the contrast-to-noise ratio between the cystic lesion and pancreatic parenchyma were calculated for all four image sets. The size of the largest cystic lesion and the diameter of pancreatic duct were measured.
A total of 63 patients were included, 48 (76.2 %) of whom had 136 pancreatic cystic lesion(s). The acquisition times of conventional HASTE and HASTEDL were 69 and 18 sec, respectively. All image quality parameters except artifacts for reader 2 were significantly better for HASTEDL with enhanced denoising. Those images also received scores for overall image quality that were significantly higher than those for the conventional HASTE (3.26 ± 0.54 vs. 2.47 ± 0.56, p < 0.001). The SNR of the pancreatic cystic lesion and pancreatic parenchyma was significantly higher in the HASTEDL with enhanced denoising (p < 0.001 for both). Inter-reader variability for measuring the pancreatic cyst size (ICC, 0.999 vs. 0.995; 95 % LoA, −0.13481 to 0.14743 vs. −0.24097 to 0.27404) and duct diameter (ICC, 0.994 vs. 0.969; 95 % LoA, −0.11684 to 0.36026 vs. −0.45544 to 0.44664) was lower in HASTEDL with enhanced denoising than in the conventional HASTE.
HASTEDL with enhanced denoising could be useful for reducing the acquisition time of pancreas MRI while improving the image quality for the evaluation of pancreatic cystic lesions.
This study aimed to quantitatively evaluate the inter-platform reproducibility and longitudinal acquisition repeatability of MRI radiomics features in Fluid-Attenuated Inversion Recovery (FLAIR), T2-weighted (T2W), and T1-weighted (T1W) sequences on MR-Linac systems using an American College of Radiology (ACR) phantom.
This study used two MR-Linac systems (A and B) in different cancer centers. The ACR phantom was scanned on system A daily for 30 consecutive days to evaluate longitudinal repeatability. Additionally, retest data were collected after repositioning the phantom. Inter-platform reproducibility was assessed by conducting scans under identical conditions using system B. Regions of interest were delineated on the T1W sequence from system A and mapped to other sequences via rigid registration. Intra-observer and inter-observer comparisons were conducted. Repeatability and reproducibility were assessed using the intraclass correlation coefficient (ICC) and coefficient of variation (CV). Robust radiomics features were identified based on ICC>0.9 and CV<10 %.
Analysis showed that a higher proportion of radiomics features derived from longitudinal FLAIR sequence (51.65 %) met robustness criteria compared to T2W (48.35 %) and T1W (43.96 %). Additionally, more inter-platform features from the FLAIR sequence (62.64 %) were robust compared to T2W (42.86 %) and T1W (39.56 %). Test-retest and intra-observer repeatability were excellent across all sequences, with a median ICC of 0.99 and CV<5%. However, inter-observer reproducibility was inferior, especially for the T1W sequence.
Different sequences show variations in repeatability and reproducibility. The FLAIR sequence demonstrated advantages in both longitudinal repeatability and inter-platform reproducibility. Caution is warranted when interpreting data, particularly in longitudinal or multiplatform radiomics studies.
Compared to conventional energy integrating detector CT, Photon-Counting CT (PCCT) has the advantage of increased spatial resolution. The pancreas is a highly complex organ anatomically. The increased spatial resolution of PCCT challenges radiologists’ knowledge of pancreatic anatomy. The purpose of this review was to review detailed macroscopic and microscopic anatomy of the pancreas in the context of current and future PCCT.
This review is based on a literature review of all parts of pancreatic anatomy and a retrospective imaging review of PCCT scans from 20 consecutively included patients without pancreatic pathology (mean age 61.8 years, 11 female), scanned in the workup of pancreatic cancer with a contrast enhanced multiphase protocol. Two radiologists assessed the visibility of the main and accessory pancreatic ducts, side ducts, ampulla, major papilla, minor papilla, pancreatic arteries and veins, regional lymph nodes, coeliac ganglia, and coeliac plexus.
The macroscopic anatomy of the pancreas was consistently visualized with PCCT. Visualization of detailed anatomy of the ductal system (including side ducts), papillae, arteries, vein, lymph nodes, and innervation was possible in 90% or more of patients with moderate to good interreader agreement.
PCCT scans of the pancreas visualizes previously unseen or inconsistently seen small anatomical structures consistently. Increased knowledge of pancreatic anatomy could have importance in imaging of pancreatic cancer and other pancreatic diseases.