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Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?
Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?
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Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?
Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?

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Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?
Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?
Journal Article

Gastro-Esophageal Cancer: Can Radiomic Parameters from Baseline 18 F-FDG-PET/CT Predict the Development of Distant Metastatic Disease?

2024
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Overview
We aimed to determine if clinical parameters and radiomics combined with sarcopenia status derived from baseline F-FDG-PET/CT could predict developing metastatic disease and overall survival (OS) in gastroesophageal cancer (GEC). Patients referred for primary staging who underwent F-FDG-PET/CT from 2008 to 2019 were evaluated retrospectively. Overall, 243 GEC patients (mean age = 64) were enrolled. Clinical, histopathology, and sarcopenia data were obtained, and primary tumor radiomics features were extracted. For classification (early-stage vs. advanced disease), the association of the studied parameters was evaluated. Various clinical and radiomics models were developed and assessed. Accuracy and area under the curve (AUC) were calculated. For OS prediction, univariable and multivariable Cox analyses were performed. The best model included PET/CT radiomics features, clinical data, and sarcopenia score (accuracy = 80%; AUC = 88%). For OS prediction, various clinical, CT, and PET features entered the multivariable analysis. Three clinical factors (advanced disease, age ≥ 70 and ECOG ≥ 2), along with one CT-derived and one PET-derived radiomics feature, retained their significance. Overall, F-FDG PET/CT radiomics seems to have a potential added value in identifying GEC patients with advanced disease and may enhance the performance of baseline clinical parameters. These features may also have a prognostic value for OS, improving the decision-making for GEC patients.

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