{"title":"Clinical contribution of 18F-FDG PET/CT in patients with pediatric bone tissue and soft tissue sarcoma; a retrospective study","authors":"M.N. Engin, G.G. Bural, E. Güler, A. Boz","doi":"10.1016/j.remnie.2025.500252","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To assess whether parameters derived from ¹⁸F-FDG PET/CT imaging could be used for prognostic evaluation in pediatric patients with bone and soft tissue sarcomas.</div></div><div><h3>Material and methods</h3><div>This retrospective study included pediatric patients diagnosed with sarcoma who underwent ¹⁸F-FDG PET/CT between February 2013 and January 2021. A total of 63 patients were evaluated. Anatomical tumor volume, standardized uptake values (SUV), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were measured. Progression-free survival (PFS) and overall survival (OS) were calculated. Cox regression analysis was performed to identify independent predictors.</div></div><div><h3>Results</h3><div>The mortality rate was 31.7%, and the median OS was 54.9 months. Lung (p<!--> <!--><<!--> <!-->0.001) and lymph node metastases (p<!--> <!-->=<!--> <!-->0.049) were associated with shorter OS. Younger age at diagnosis (p<!--> <!-->=<!--> <!-->0.014), higher anatomical tumor volume (p<!--> <!-->=<!--> <!-->0.002), and lung metastasis (p<!--> <!-->=<!--> <!-->0.004) were independently associated with increased mortality risk. High MTV was independently associated with higher progression risk (p<!--> <!--><<!--> <!-->0.001).</div></div><div><h3>Conclusion</h3><div>Anatomical tumor volume and lung metastasis predict mortality, while MTV predicts progression in pediatric sarcoma. Further prospective studies are needed to validate these findings.</div></div>","PeriodicalId":94197,"journal":{"name":"Revista espanola de medicina nuclear e imagen molecular","volume":"45 4","pages":"Article 500252"},"PeriodicalIF":0.0000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista espanola de medicina nuclear e imagen molecular","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2253808925001600","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/11/26 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
To assess whether parameters derived from ¹⁸F-FDG PET/CT imaging could be used for prognostic evaluation in pediatric patients with bone and soft tissue sarcomas.
Material and methods
This retrospective study included pediatric patients diagnosed with sarcoma who underwent ¹⁸F-FDG PET/CT between February 2013 and January 2021. A total of 63 patients were evaluated. Anatomical tumor volume, standardized uptake values (SUV), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were measured. Progression-free survival (PFS) and overall survival (OS) were calculated. Cox regression analysis was performed to identify independent predictors.
Results
The mortality rate was 31.7%, and the median OS was 54.9 months. Lung (p < 0.001) and lymph node metastases (p = 0.049) were associated with shorter OS. Younger age at diagnosis (p = 0.014), higher anatomical tumor volume (p = 0.002), and lung metastasis (p = 0.004) were independently associated with increased mortality risk. High MTV was independently associated with higher progression risk (p < 0.001).
Conclusion
Anatomical tumor volume and lung metastasis predict mortality, while MTV predicts progression in pediatric sarcoma. Further prospective studies are needed to validate these findings.