This study aims to refine the molecular classification of thyroid cancer (TC) using a multi-omics approach. By identifying a novel gene set and applying decision-tree modeling, the study seeks to improve diagnostic accuracy and predict tumor progression in BRAFV600E-like and RAS-like TC subtypes. Protein biomarkers were validated via immunohistochemistry (IHC), with findings confirmed across external datasets.
Study Type
OBSERVATIONAL
Enrollment
275
Seoul National University Hospital
Seoul, South Korea
Classification Accuracy of Gene-Based Model
The accuracy of the decision-tree model using specific gene set to classify thyroid cancer into BRAFV600E-like, RAS-like, and NT (normal thyroid) -like subtypes. Model performance will be evaluated using accuracy, sensitivity, specificity, and Cohen's kappa.
Time frame: 1 year
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