ABSTRACT
Purpose: This study aims to explore the value of clinical features, CT imaging signs, and radiomics features in differentiating between adults and children with Mycoplasma pneumonia and seeking quantitative radiomic representations of CT imaging signs. Materials and methods: In a retrospective analysis of 981 cases of mycoplasmal pneumonia patients from November 2021 to December 2023, 590 internal data (adults:450, children: 140) randomly divided into a training set and a validation set with an 8:2 ratio and 391 external test data (adults:121; children:270) were included. Using univariate analysis, CT imaging signs and clinical features with significant differences (p < 0.05) were selected. After segmenting the lesion area on the CT image as the region of interest, 1,904 radiomic features were extracted. Then, Pearson correlation analysis (PCC) and the least absolute shrinkage and selection operator (LASSO) were used to select the radiomic features. Based on the selected features, multivariable logistic regression analysis was used to establish the clinical model, CT image model, radiomic model, and combined model. The predictive performance of each model was evaluated using ROC curves, AUC, sensitivity, specificity, accuracy, and precision. The AUC between each model was compared using the Delong test. Importantly, the radiomics features and quantitative and qualitative CT image features were analyzed using Pearson correlation analysis and analysis of variance, respectively. Results: For the individual model, the radiomics model, which was built using 45 selected features, achieved the highest AUCs in the training set, validation set, and external test set, which were 0.995 (0.992, 0.998), 0.952 (0.921, 0.978), and 0.969 (0.953, 0.982), respectively. In all models, the combined model achieved the highest AUCs, which were 0.996 (0.993, 0.998), 0.972 (0.942, 0.995), and 0.986 (0.976, 0.993) in the training set, validation set, and test set, respectively. In addition, we selected 11 radiomics features and CT image features with a correlation coefficient r greater than 0.35. Conclusion: The combined model has good diagnostic performance for differentiating between adults and children with mycoplasmal pneumonia, and different CT imaging signs are quantitatively represented by radiomics.
ABSTRACT
Background: This study investigated the value of a deep learning (DL) model based on computed tomography (CT) enhancement for predicting human epidermal growth factor receptor 2 (HER2) expression in patients with liver metastasis from breast cancer. Methods: Data were collected for 151 female patients with liver metastasis from breast cancer who underwent abdominal enhanced CT examination in the Department of Radiology at the Affiliated Hospital of Hebei University between January 2017 and March 2022. Liver metastases were confirmed in all patients by pathology. The HER2 status of the liver metastases was assessed and enhanced CT examinations were performed before treatment. Of the 151 patients, 93 were HER2 negative and 58 were HER2 positive. Liver metastases were manually labeled with rectangular frames, layer by layer, and the labeled data were processed. Five basic networks (ResNet34, ResNet50, ResNet101, ResNeXt50, and Swim Transformer) were used for training and optimization, and the model's performance was tested. Receiver operating characteristic (ROC) curves were used to analyze the area under the curve (AUC), as well as the accuracy, sensitivity, and specificity of the networks in predicting HER2 expression in breast cancer liver metastases. Results: Overall, ResNet34 demonstrated the best prediction efficiency. The accuracy of the validation and test set models in predicting HER2 expression in liver metastases was 87.4% and 80.5%, respectively. The AUC, sensitivity, and specificity of the test set model in predicting HER2 expression in liver metastases were 0.778, 77.0%, and 84.0%, respectively. Conclusions: Our DL model based on CT enhancement has good stability and diagnostic efficacy, and is a potential non-invasive method for identifying HER2 expression in liver metastases from breast cancer.
