A comparison of 2D and 3D magnetic resonance imaging-based intratumoral and peritumoral radiomics models for the prognostic prediction of endometrial cancer: a pilot study
Accurate prognostic assessment is vital for the personalized treatment of endometrial cancer (EC). Although radiomics models have demonstrated prognostic potential in EC, the impact of region of interest (ROI) delineation strategies and the clinical significance of peritumoral features remain uncert...
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Veröffentlicht in: | Cancer imaging 2024-07, Vol.24 (1), p.100-10, Article 100 |
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Sprache: | eng |
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Zusammenfassung: | Accurate prognostic assessment is vital for the personalized treatment of endometrial cancer (EC). Although radiomics models have demonstrated prognostic potential in EC, the impact of region of interest (ROI) delineation strategies and the clinical significance of peritumoral features remain uncertain. Our study thereby aimed to explore the predictive performance of varying radiomics models for the prediction of LVSI, DMI, and disease stage in EC.
Patients with 174 histopathology-confirmed EC were retrospectively reviewed. ROIs were manually delineated using the 2D and 3D approach on T2-weighted MRI images. Six radiomics models involving intratumoral (2D
and 3D
), peritumoral (2D
and 3D
), and combined models (2D
and 3D
) were developed. Models were constructed using the logistic regression method with five-fold cross-validation. Area under the receiver operating characteristic curve (AUC) was assessed, and was compared using the Delong's test.
No significant differences in AUC were observed between the 2D
and 3D
models, or the 2D
and 3D
models in all prediction tasks (P > 0.05). Significant difference was observed between the 3D
and 3D
models for LVSI (0.738 vs. 0.805) and DMI prediction (0.719 vs. 0.804). The 3D
models demonstrated significantly better predictive performance in all 3 prediction tasks compared to the 3D
model in both the training and validation cohorts (P |
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ISSN: | 1470-7330 1740-5025 1470-7330 |
DOI: | 10.1186/s40644-024-00743-2 |