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Role of positron emission tomography and bone scintigraphy in the evaluation of bone involvement in metastatic pheochromocytoma and paraganglioma: specific implications for succinate dehydrogenase enzyme subunit B gene mutations

Tomáš ZelinkaReproductive Biology and Medicine Branch, NICHD, NINDS, NIH, Bethesda, MD 20892, USAHenri TimmersReproductive Biology and Medicine Branch, National Institutes of Child Health and Human Development,Anna KozupaReproductive Biology and Medicine Branch , National Institutes of Child Health and Human Development ,Chao Ping ChenNuclear Medicine Department ,Jorge A. CarrasquilloNuclear Medicine Department ,James C. ReynoldsNuclear Medicine Department ,Alexander LingG. EisenhoferClinical Neurocardiology Section , National Institute of Neurological Disorders and Stroke , National Institutes of Health , Bethesda , Maryland 20892 , USAIvica LazúrováKaren T. AdamsReproductive Biology and Medicine Branch, National Institutes of Child Health and Human Development,Millie WhatleyNuclear Medicine Department ,J WidimskýKarel PacákNational Institutes of Health
2008en
ABI

Аннотация

We performed a retrospective analysis of 71 subjects with metastatic pheochromocytoma and paraganglioma (30 subjects with mutation of succinate dehydrogenase enzyme subunit B (SDHB) gene and 41 subjects without SDHB mutation). Sixty-nine percent presented with bone metastases (SDHB +/-: 77% vs 63%), 39% with liver metastases (SDHB +/-: 27% vs 47%), and 32% with lung metastases (SDHB +/-: 37% vs 29%). The most common sites of bone involvement were thoracic spine (80%; SDHB+/-: 83% vs 77%), lumbar spine (78%; SDHB +/-: 78% vs 75%), and pelvic and sacral bones (78%; SDHB +/-: 91% vs 65%, P=0.04). Subjects with SDHB mutation also showed significantly higher involvement of long bones (SDHB +/-: 78% vs 30%, P=0.007) than those without the mutation. The best overall sensitivity in detecting bone metastases demonstrated positron emission tomography (PET) with 6-[(18)F]-fluorodopamine ([(18)F]-FDA; 90%), followed by bone scintigraphy (82%), computed tomography or magnetic resonance imaging (CT/MRI; 78%), 2-[(18)F]-fluoro-2-deoxy-d-glucose ([(18)F]-FDG) PET (76%), and scintigraphy with [(123/131)I]-metaiodobenzylguanidine (71%). In subjects with SDHB mutation, imaging modalities with best sensitivities for detecting bone metastases were CT/MRI (96%), bone scintigraphy (95%), and [(18)F]-FDG PET (92%). In subjects without SDHB mutations, the modality with the best sensitivity for bone metastases was [(18)F]-FDA PET (100%). In conclusion, bone scintigraphy should be used in the staging of patients with malignant pheochromocytoma and paraganglioma, particularly in patients with SDHB mutations. As for PET imaging, [(18)F]-FDG PET is highly recommended in SDHB mutation patients, whereas [(18)F]-FDA PET is recommended in patients without the mutation.

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