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First published online August 18, 2009, 10.2967/jnumed.108.058701
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Journal of Nuclear Medicine Vol. 50 No. 9 1448-1454
© 2009 by Society of Nuclear Medicine

doi: 10.2967/jnumed.108.058701

Clinical Investigation

Usefulness of 123I-MIBG Scintigraphy in the Evaluation of Patients with Known or Suspected Primary or Metastatic Pheochromocytoma or Paraganglioma: Results from a Prospective Multicenter Trial

Gregory A. Wiseman1, Karel Pacak2, Mary S. O'Dorisio3, Donald R. Neumann4, Alan D. Waxman5, David A. Mankoff6, Sherif I. Heiba7, Aldo N. Serafini8, Sabah S. Tumeh9, Natalie Khutoryansky10 and Arnold F. Jacobson10

1 Department of Nuclear Medicine, Mayo Clinic, Rochester, Minnesota; 2 Reproductive and Adult Endocrinology Program, National Institute of Child Health and Development, National Institutes of Health, Bethesda, Maryland; 3 Department of Pediatrics, University of Iowa, Iowa City, Iowa; 4 Department of Nuclear Medicine, Cleveland Clinic, Cleveland, Ohio; 5 Department of Nuclear Medicine, Cedars-Sinai Medical Center, Los Angeles, California; 6 Department of Radiology, University of Washington, Seattle, Washington; 7 Department of Nuclear Medicine, Mount Sinai Medical Center, New York, New York; 8 Department of Nuclear Medicine, University of Miami, Miami, Florida; 9 Department of Radiology, Piedmont Hospital, Atlanta, Georgia; and 10 Research and Development, GE Healthcare, Princeton, New Jersey

Correspondence: For correspondence or reprints contact: Arnold F. Jacobson, GE Healthcare Medical Diagnostics, 101 Carnegie Center, Princeton, NJ 08540. E-mail: arnold.jacobson{at}ge.com

Although 123I-MIBG has been in clinical use for the imaging of pheochromocytoma for many years, a large multicenter evaluation of this agent has never been performed. The present study was designed to provide a prospective confirmation of the performance of 123I-MIBG scintigraphy for the evaluation of patients with known or suspected primary or metastatic pheochromocytoma or paraganglioma. Methods: A total of 81 patients with a prior history of primary or metastatic pheochromocytoma or paraganglioma and 69 with suspected pheochromocytoma or paraganglioma based on symptoms of catecholamine excess, CT or MRI findings, or elevated catecholamine or metanephrine levels underwent whole-body planar and selected SPECT 24 h after the administration of 123I-MIBG. Images were independently interpreted by 3 masked readers, with consensus requiring agreement of at least 2 readers. Final diagnoses were based on histopathology, correlative imaging, catecholamine or metanephrine measurements, and clinical follow-up. Results: Among 140 patients with definitive diagnoses (91, disease present; 49, disease absent), 123I-MIBG planar scintigraphy had a sensitivity and specificity of 82%. For patients evaluated for suspected disease, sensitivity and specificity were 88% and 84%, respectively. For the subpopulations of adrenal (pheochromocytoma) and extraadrenal (paraganglioma) tumors, sensitivities were 88% and 67%, respectively. The addition of SPECT increased reader confidence but minimally affected sensitivity and specificity. Conclusion: This prospective study demonstrated a sensitivity of 82%–88% and specificity of 82%–84% for 123I-MIBG imaging used in the diagnostic assessment of primary or metastatic pheochromocytoma or paraganglioma.

Key Words: 123I-MIBG • scintigraphy • pheochromocytoma • paraganglioma • neuroendocrine tumors

COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.


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