Extending positron emission tomography scan utility to high-risk neuroblastoma: Fluorine-18 fluorodeoxyglucose positron emission tomography as sole imaging modality in follow-up of patients

被引:107
作者
Kushner, BH
Yeung, HWD
Larson, SM
Kramer, K
Cheung, NKV
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med Imaging, New York, NY 10021 USA
关键词
D O I
10.1200/JCO.2001.19.14.3397
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Although positron emission tomography (PET) with fluorine-18 fluorodeoxyglucose (F-18-FDG) has a major impact on the treatment of adult cancer, the reported experience with extracranial tumors of childhood is limited. We describe a role for PET in patients with neuroblastoma (NB). patients and Methods: In 51 patients with high-risk NE, 92 PET scans were part of a staging evaluation that included iodine-123 or iodine-131 metaiodobenzylguanidine (MIBG) scan, bone scan, computed tomography (and/or magnetic resonance imaging), urine catecholamine measurements, and bone marrow (BM) examinations. The minimum number of tests sufficient to detect Nh wets determined. Results: Of 40 patients who were not in complete remission, only 1 (2.5%) had NE that would have been missed had a staging evaluation been limited to PET and BM studies, and 13 (32.5%) had NE detected by PET but nor by BM and urine tests. PET wets equal or superior to MIBG scans for identifying NE in soft tissue and extracranial skeletal structures, for revealing small lesions, and for delineating the extent and localizing sites of disease. In 36 evaluations of 22 patients with NE in soft tissue, PET failed to identify only two long-standing MIBG-negative abdominal masses. PET and MIBG scans showed more skeletal lesions than bone scans, but the normally high physiologic brain uptake of FDG blocked PET visualization of cranial vault lesions. Similar to MIBG, FDG skeletal uptake was diffusely increased with extensive or progressing BM disease but faint or absent with minimal or nonprogressing BM disease. Conclusion: In the absence or after resolution of cranial vault lesions, and once the primary tumor is resected, PET and BM tests suffice for monitoring NE patients at high risk for progressive disease in soft tissue and bone/BM. (C) 2001 by American Society of Clinical Oncology.
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页码:3397 / 3405
页数:9
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