Abstract
To develop and validate a radiomics nomogram model for predicting the micropapillary pattern (MPP) in lung adenocarcinoma (LUAD) tumors of ≤2 cm in size. In this study, 300 LUAD patients from our institution were randomly divided into the training cohort (n = 210) and an internal validation cohort (n = 90) at a ratio of 7:3, besides, we selected 65 patients from another hospital as the external validation cohort. The region of interest of the tumor was delineated on the computed tomography (CT) images, and radiomics features were extracted. A nomogram model was established using radiomics features, clinical features and conventional radiographic features. The nomogram model was compared with the radiomics model and the clinical model alone to test its diagnostic validity. Receiver operating characteristic (ROC) curves, areas under the ROC curves and decision curve analysis (DCA) results were plotted to evaluate the model performance and clinical application. The nomogram model exhibited superior performance, with an AUC of 0.905 (95% confidence interval [CI]: 0.857-0.951) in the training cohort, which decreased to 0.817 (95% CI: 0.698-0.936) in the external validation cohort. The clinical model had AUCs of 0.820 (95% CI: 0.753-0.886) and 0.730 (95% CI: 0.572-0.888) in the training and external validation cohorts, respectively. The radiomics model had AUCs of 0.895 (95% CI: 0.840-0.949) and 0.800 (95% CI: 0.675-0.924) for training and external validation, respectively. DCA confirmed that the nomogram model had the better clinical benefit. The nomogram model achieved promising prediction efficiency for identifying the presence of the MPP in LUAD tumors ≤2 cm, allowing clinicians to develop more rational and efficacious personalized treatment strategies.
Published Version
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