4.6 Article

Multi-Parameter MR Radiomics Based Model to Predict 5-Year Progression-Free Survival in Endometrial Cancer

期刊

FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.813069

关键词

endometrial cancer; progression-free survival; radiomics; magnetic resonance imaging; nomogram

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资金

  1. National Natural Science Foundation of China [81871029]
  2. Scientific Research Fund Project of Health Commission of Hebei Province [20200138]

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In this study, a multi-parameter MRI radiomics-based nomogram model was developed to predict 5-year progression-free survival in patients with resected endometrial cancer. The model, incorporating radiomics features, clinical factors, and conventional MR findings, demonstrated good calibration and discrimination ability.
Background: Relapse is the major cause of mortality in patients with resected endometrial cancer (EC). There is an urgent need for a feasible method to identify patients with high risk of relapse. Purpose: To develop a multi-parameter magnetic resonance imaging (MRI) radiomics-based nomogram model to predict 5-year progression-free survival (PFS) in EC. Methods: For this retrospective study, 202 patients with EC followed up for at least 5 years after hysterectomy. A radiomics signature was extracted from T2-weighted imaging (T2WI), apparent diffusion coefficient (ADC) and a dynamic contrast-enhanced three-dimensional volumetric interpolated breath-hold examination (3D-VIBE). The radiomics score (RS) was calculated based on the least absolute shrinkage and selection operator (LASSO) regression. We have developed a radiomics based nomogram model (Model(N)) incorporating the RS and clinical and conventional MR (cMR) risk factors. The performance was evaluated by the receiver operating characteristic curve (ROC), calibration curve and decision curve analysis (DCA). Results: The Model(N) demonstrated a good calibration and satisfactory discrimination, with a mean area under the curve (AUC) of 0.840 and 0.958 in the training and test cohorts, respectively. In comparison with clinical prediction model (Model(C)), the discrimination ability of Model showed an improvement with P < 0.001 for the training cohort and P=0.032 for the test cohort. Compared to the radiomics prediction model (Model(R)), Model(N) discrimination ability showed an improvement for the training cohort with P = 0.021, with no statistically significant difference in the test cohort (P = 0.106). Calibration curves suggested a good fit for probability (Hosmer-Lemeshow test, P = 0.610 and P = 0.956 for the training and test cohorts, respectively). Conclusion: This multi-parameter nomogram model incorporating clinical and cMR findings is a valid method to predict 5-year PFS in patients with EC.

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