Clinical experience with 18F-fluorodeoxyglucose positron emission tomography and 123I-metaiodobenzylguanine scintigraphy in pediatric neuroblastoma: complementary roles in follow-up of patients

Korean Journal of Pediatrics 2014³â 57±Ç 6È£ p.278 ~ p.286

±æÅ¿µ(Gil Tae-Young) - Ewha Womans University School of Medicine Ewha Womans University Mokdong Hospital Department of Pediatrics
À̵µ°æ(Lee Do-Kyung) - Ewha Womans University School of Medicine Ewha Womans University Mokdong Hospital Department of Pediatrics
ÀÌÁ¤¹Î(Lee Jung-Min) - Ewha Womans University School of Medicine Ewha Womans University Mokdong Hospital Department of Pediatrics
À¯Àº¼±(Yoo Eun-Sun) - Ewha Womans University School of Medicine Ewha Womans University Mokdong Hospital Department of Pediatrics
À¯°æÇÏ(Ryu Kyung-Ha) - Ewha Womans University School of Medicine Ewha Womans University Mokdong Hospital Department of Pediatrics

Abstract

Purpose: To evaluate the potential utility of 123I-metaiodobenzylguanine (123I-MIBG) scintigraphy and 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) for the detection of primary and metastatic lesions in pediatric neuroblastoma (NBL) patients, and to determine whether 18F-FDG PET is as beneficial as 123I-MIBG imaging.

Methods: We selected 8 NBL patients with significant residual mass after operation and who had paired 123I-MIBG and 18F-FDG PET images that were obtained during the follow-up. We retrospectively reviewed the clinical charts and the findings of 45 paired scans.

Results: Both scans correlated relatively well with the disease status as determined by standard imaging modalities during follow-up; the overall concordance rates were 32/45 (71.1%) for primary tumor sites and 33/45 (73.3%) for bone-bone marrow (BM) metastatic sites. In detecting primary tumor sites, 123IMIBG might be superior to 18F-FDG PET. The sensitivity of 123I-MIBG and 18F-FDG PET were 96.7% and 70.9%, respectively, and their specificity were 85.7% and 92.8%, respectively. 18F-FDG PET failed to detect 9 true NBL lesions in 45 follow-up scans (false negative rate, 29%) with positive 123I-MIBG. For bone-BM metastatic sites, the sensitivity of 123I-MIBG and F18-FDG PET were 72.7% and 81.8%, respectively, and the specificity were 79.1% and 100%, respectively. 123I-MIBG scans showed higher false positivity (20.8%) than 18F-FDG PET (0%).

Conclusion: 123I-MIBG is superior for delineating primary tumor sites, and 18F-FDG PET could aid in discriminating inconclusive findings on bony metastatic NBL. Both scans can be complementarily used to clearly determine discrepancies or inconclusive findings on primary or bone-BM metastatic NBL during follow-up.

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Neuroblastoma, Positron emission tomography, MIBG, Child, Follow-up studies
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