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        <identifier>oai:figshare.com:article/33717790</identifier>
        <datestamp>2026-09-14T04:31:33Z</datestamp>
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          <dc:title>Data Sheet 1_MRI-derived deep-feature model for differentiating stage I endometrial carcinoma from atypical endometrial hyperplasia: a two-center retrospective study.pdf</dc:title>
          <dc:creator>Danhong Chai (24867712)</dc:creator>
          <dc:creator>Fenghua Ma (14783455)</dc:creator>
          <dc:creator>Yan Chen (4308)</dc:creator>
          <dc:creator>Yapei Zhong (24867715)</dc:creator>
          <dc:creator>Guofu Zhang (463042)</dc:creator>
          <dc:creator>Zhaoxia Qian (1417342)</dc:creator>
          <dc:creator>Jinwei Qiang (3147915)</dc:creator>
          <dc:subject>Oncology and Carcinogenesis not elsewhere classified</dc:subject>
          <dc:subject>atypical endometrial hyperplasia</dc:subject>
          <dc:subject>deep learning</dc:subject>
          <dc:subject>endometrial carcinoma</dc:subject>
          <dc:subject>magnetic resonance imaging</dc:subject>
          <dc:subject>radiomics</dc:subject>
          <dc:description>Background&lt;p&gt;Differentiating stage I endometrial carcinoma (EC) from atypical endometrial hyperplasia (AEH) before surgery is critical for guiding treatment decisions, yet current magnetic resonance imaging (MRI) assessment is limited by overlapping appearances and inter-observer variability.&lt;/p&gt;Methods&lt;p&gt;In this retrospective, two-center study, 297 patients (153 stage I EC and 144 AEH) who underwent multiparametric MRI were included. Radiomics features were extracted from T2-weighted imaging with fat saturation (T2WI-FS), diffusion-weighted imaging (DWI), apparent diffusion coefficient (ADC) map, and contrast-enhanced T1-weighted imaging (CE-T1WI) sequences. Feature selections were performed using univariate filtering, correlation analysis, least absolute shrinkage and selection operator (LASSO) and multivariate stepwise regression. A Radiomics model, a Clin+Rad model, and a DenseNet121-derived deep-feature model were constructed and compared for differentiating stage I EC from AEH. Model performance was evaluated using receiver operating characteristic (ROC) curves, calibration curves, decision curve analysis (DCA).&lt;/p&gt;Results&lt;p&gt;Seven radiomics features and eight deep-learning features were ultimately selected to construct the models. In the external validation cohort, the DenseNet121-derived deep-feature model achieved the numerically highest AUC of 0.854 (95% CI, 0.743-0.965), compared with 0.803 (95% CI, 0.673-0.933) for the Radiomics model and 0.773 (95% CI, 0.626-0.919) for the Clin+Rad model, although the pairwise differences in AUC were not statistically significant. In addition, the DenseNet121-derived model showed a relatively greater net clinical benefit at threshold probabilities of approximately 0.15-0.80. SHAP analysis indicated that several influential deep features were derived from ADC images, suggesting that ADC-derived features contributed substantially to the model predictions.&lt;/p&gt;Conclusions&lt;p&gt;The DenseNet121-derived model achieved the numerically highest AUC in the external validation cohort, although the pairwise differences were not statistically significant, indicating its potential as a non-invasive tool to support individualized decision-making.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T04:31:33Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fonc.2026.1943943.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_MRI-derived_deep-feature_model_for_differentiating_stage_I_endometrial_carcinoma_from_atypical_endometrial_hyperplasia_a_two-center_retrospective_study_pdf/33717790</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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