4.5 Article

A Radiomics Nomogram for Non-Invasive Prediction of Progression-Free Survival in Esophageal Squamous Cell Carcinoma

Journal

FRONTIERS IN COMPUTATIONAL NEUROSCIENCE
Volume 16, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fncom.2022.885091

Keywords

esophageal squamous cell carcinoma; computed tomography; progression-free survival; radiomics; nomogram

Funding

  1. National Natural Science Foundation of China [62176177, 81702449]
  2. Fundamental Research Program of Shanxi Province [20210302123292, 20210302123112]
  3. Shanxi Scholarship Council of China [2021-039]
  4. Central Guidance on Local Science and Technology Development Fund of Shanxi Province [YDZJSX2021A018]
  5. Shenzhen Project of Science and Technology [JCYJ20190813094203600]

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By using radiomics features and traditional TNM staging, we successfully constructed a prognostic model for predicting esophageal squamous cell carcinoma (ESCC), which demonstrated good predictive ability in both the training and validation cohorts.
To construct a prognostic model for preoperative prediction on computed tomography (CT) images of esophageal squamous cell carcinoma (ESCC), we created radiomics signature with high throughput radiomics features extracted from CT images of 272 patients (204 in training and 68 in validation cohort). Multivariable logistic regression was applied to build the radiomics signature and the predictive nomogram model, which was composed of radiomics signature, traditional TNM stage, and clinical features. A total of 21 radiomics features were selected from 954 to build a radiomics signature which was significantly associated with progression-free survival (p < 0.001). The area under the curve of performance was 0.878 (95% CI: 0.831-0.924) for the training cohort and 0.857 (95% CI: 0.767-0.947) for the validation cohort. The radscore of signatures' combination showed significant discrimination for survival status. Radiomics nomogram combined radscore with TNM staging and showed considerable improvement over TNM staging alone in the training cohort (C-index, 0.770 vs. 0.603; p < 0.05), and it is the same with clinical data (C-index, 0.792 vs. 0.680; p < 0.05), which were confirmed in the validation cohort. Decision curve analysis showed that the model would receive a benefit when the threshold probability was between 0 and 0.9. Collectively, multiparametric CT-based radiomics nomograms provided improved prognostic ability in ESCC.

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