Abstract
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Objectives This study aimed to evaluate F-18 fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) as an adjunct to CT and/or magnetic resonance imaging (MRI) in the staging and follow-up of pediatric rhabdomyosarcoma (RMS).
Methods A total of 28 consecutive pediatric RMS (20 males, 8 female; mean age, 4.8 years, 10 embryonal,18 alveolar), in whom FDG PET/CT was performed at staging, evaluation of therapeutic effects and follow-up, were retrospectively included. FDG PET/CT was compared with MRI, CT performed with a less than a 10-day interval for initial staging in 13 patients. Histological data and follow-up (mean, 18 months) were considered as the standard of reference for result interpretation.
Results At staging, FDG PET/CT and CT/MRI were equally effective in the detection of the primary RMS (accuracy, 100%). FDG PET/CT revealed metastases in lymph nodes, prostate, intestinal wall, chest wall and the peritoneum in 5 patients missed by CT or MRI, and found 41positive lymph node territories in 6 patients, 8 lung metastases in 3 patients and 40 bone, muscle, brain, etc in 4 patients versus 16, 6, and 29, respectively, with CT or MRI. On the whole analysis, FDG PET/CT modified lymph node staging in 4 of 13 patients. The significant high SUVmax of primary tumor and more metastases were found in alveolar RMS(ARMS). In 4 patients (31%), modifications were made and comprised 1 local therapy change and 3 changes of systemic treatment as well. Four patients (4/11) achieved complete metabolic response on FDG PET/CT and 2 were partial responders on FDG PET/CT.
Conclusions FDG PET/CT is useful in staging and restaging pediatric RMS, especially for assessing lymph nodes and prostate involvement with potential therapeutic strategy alteration. The significant high SUVmax of ARMS and more metastases may indicate worse prognosis which needs further study. This study confirms that FDG PET/CT is also valuable in therapeutic assessment and follow-up.
Research Support National Natural Science Fund (grant 51233007,81271612 and 81401439), Shanghai Pujiang Program (grant 13PJD022), and Shanghai Health Bureau Fund (grant 20124016).