Predicting persistent/recurrent cervical lymph node metastasis in papillary thyroid carcinoma with PET/CT-based multimodal radiomics: an image-pathology matching study.
[OBJECTIVE] Current evidence regarding radiomics-based assessment of persistent/recurrent cervical lymph node metastasis (CLNM) remains limited, particularly in the field of PET/CT in papillary thyroi
APA
Chen P, Duan Y, et al. (2026). Predicting persistent/recurrent cervical lymph node metastasis in papillary thyroid carcinoma with PET/CT-based multimodal radiomics: an image-pathology matching study.. Nuclear medicine communications. https://doi.org/10.1097/MNM.0000000000002124
MLA
Chen P, et al.. "Predicting persistent/recurrent cervical lymph node metastasis in papillary thyroid carcinoma with PET/CT-based multimodal radiomics: an image-pathology matching study.." Nuclear medicine communications, 2026.
PMID
41709651
Abstract
[OBJECTIVE] Current evidence regarding radiomics-based assessment of persistent/recurrent cervical lymph node metastasis (CLNM) remains limited, particularly in the field of PET/CT in papillary thyroid cancer (PTC). Therefore, we aimed to construct a prediction model for persistent/recurrent CLNM of PTC by fluoro-18-deoxyglucose (18F-FDG) PET/computed tomography (CT) multimodal radiomics.
[METHODS] We retrospectively analyzed postoperative patients with PTC who underwent 18F-FDG PET/CT at our hospital between June 2021 and June 2024. A total of 425 CLNs (219 metastatic and 206 nonmetastatic) from 158 patients were included, and the patients were randomly assigned to a training set and a test set at a ratio of 7 : 3. Pearson correlation analysis and least absolute shrinkage and selection operator regression were utilized to select PET/CT radiomic features for model development. Five radiomics models were developed based on distinct feature sets: clinical features alone, CT radiomics, PET radiomics, PET/CT radiomics, and integrated PET/CT radiomics combined with clinical features. Subsequently, a nomogram model was built by combining radscore and clinical features.
[RESULTS] The integrated model demonstrated superior diagnostic accuracy, with areas under the curve (AUCs) of 0.944 in the training set and 0.922 in the test set. PET/CT models demonstrated the following AUCs: PET/CT (0.887), PET (0.834), CT (0.775), and clinical features alone (0.783). A nomogram incorporating clinical features and radscores was then developed, achieving C-indices of 0.937 in the training set and 0.895 in the test set.
[CONCLUSION] The integration of PET/CT radiomics and clinical features may provide a noninvasive tool for predicting persistent/recurrent CLNM in postoperative PTC patients, with potential to support clinical decision‑making.
[METHODS] We retrospectively analyzed postoperative patients with PTC who underwent 18F-FDG PET/CT at our hospital between June 2021 and June 2024. A total of 425 CLNs (219 metastatic and 206 nonmetastatic) from 158 patients were included, and the patients were randomly assigned to a training set and a test set at a ratio of 7 : 3. Pearson correlation analysis and least absolute shrinkage and selection operator regression were utilized to select PET/CT radiomic features for model development. Five radiomics models were developed based on distinct feature sets: clinical features alone, CT radiomics, PET radiomics, PET/CT radiomics, and integrated PET/CT radiomics combined with clinical features. Subsequently, a nomogram model was built by combining radscore and clinical features.
[RESULTS] The integrated model demonstrated superior diagnostic accuracy, with areas under the curve (AUCs) of 0.944 in the training set and 0.922 in the test set. PET/CT models demonstrated the following AUCs: PET/CT (0.887), PET (0.834), CT (0.775), and clinical features alone (0.783). A nomogram incorporating clinical features and radscores was then developed, achieving C-indices of 0.937 in the training set and 0.895 in the test set.
[CONCLUSION] The integration of PET/CT radiomics and clinical features may provide a noninvasive tool for predicting persistent/recurrent CLNM in postoperative PTC patients, with potential to support clinical decision‑making.
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