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Determining Glucose Metabolism Kinetics Using 18F-FDG Micro-PET/CT
Published on: May 2, 2017
Added predictive value of 18F-FDG PET/CT for pediatric rhabdomyosarcoma
Esraa El-Kholy1,2, Enas El Nadi3,4, Hanafy Hafez4
1Nuclear Medicine and Radiation Oncology Department, National Cancer Institute (NCI), Cairo University.
Insights
Higher fluorine-18-fluorodeoxyglucose (F-FDG) standardized uptake value (SUV) in pediatric rhabdomyosarcoma (RMS) indicates a worse prognosis. This finding suggests F-FDG PET/CT can aid in predicting outcomes for RMS patients.
Area of Science:
- Nuclear Medicine
- Pediatric Oncology
- Radiology
Background:
- Pediatric rhabdomyosarcoma (RMS) is a significant childhood cancer.
- Accurate prognostic markers are crucial for tailoring treatment strategies in pediatric RMS.
- Fluorine-18-fluorodeoxyglucose (F-FDG) Positron Emission Tomography/Computed Tomography (PET/CT) is increasingly used in oncology.
Purpose of the Study:
- To evaluate the prognostic significance of quantitative F-FDG standardized uptake value (SUV) in pediatric RMS patients.
- To determine if SUVmax and primary/liver SUVmax ratio can predict event-free survival (EFS) and overall survival (OS).
Main Methods:
- Retrospective analysis of 98 pediatric RMS patients who underwent initial staging PET/CT.
- Assessment of primary SUVmax and primary/liver SUVmax ratio as predictors of 36-month EFS and OS.
- Utilized receiver operating characteristic (ROC) curve analysis, univariate, and multivariate analyses.
Main Results:
- Higher SUVmax correlated with regional/distant metastasis and poorer prognosis.
- Cut-off values for primary SUVmax (3.6) and primary/liver SUVmax ratio (2.1) were identified.
- Lower SUVmax values were associated with improved EFS and OS, though statistical significance varied.
- High SUVmax was linked to unfavorable clinical and pathological features.
Conclusions:
- F-FDG PET/CT quantitative parameters, specifically SUVmax, show prognostic value in pediatric RMS.
- Elevated F-FDG uptake suggests a worse outcome and correlates with adverse prognostic factors.
- F-FDG PET/CT can serve as an additional tool for predicting outcomes in RMS patients.
Objective:
To determine the prognostic value of quantitative fluorine-18-fluorodeoxyglucose (F-FDG) standardized uptake value (SUV) in patients with pediatric rhabdomyosarcoma (RMS).
Patients And Methods:
Consecutive 98 (50 males and 48 females) (age range: 4 months to 17.5 years, mean age: 5.8 ± 4.5) patients with pathologically proven RMS who underwent PET/computed tomography for initial staging were retrospectively assessed for whether primary SUVmax and the primary/liver SUVmax ratio could predict event-free survival (EFS) and overall survival (OS) for 36 months using receiver operating characteristic curve analysis. Univariate and multivariate analyses were used to determine the reliability of these metabolic parameters and various clinical factors.
Results:
Higher SUVmax was significantly related to the presence of regional or distant metastasis with worse prognosis. With receiver operating characteristic curve marked cut-off values of 3.6 and 2.1 for primary SUVmax and the primary/liver SUVmax ratio, respectively, both EFS and OS proved to be higher in patients with SUVmax ranked below the determinate values. Patients with a primary/liver SUVmax ratio below the cut-off value of 2.1 had OS (60.8%) and EFS (48.1%) compared with 44.5 and 14.8% for patients with lesions exceeding the cut-off point of uptake; however, this failed to achieve statistical significance. In the evaluation of primary SUVmax, similar results were obtained with P values of 0.76 and 0.62, respectively. High SUVmax was more prevalent among patients with less favorable clinical and pathological features including unfavorable primary site, alveolar pathology, and high-risk group.
Conclusion:
F-FDG PET/computed tomography may be considered an additional prognostic predictor of outcome in RMS patients, where higher F-FDG uptake seems to be linked to lower survival and correlated to different unfavorable parameters.
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