HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

6-[F-18]Fluoro-L-dihydroxyphenylalanine positron emission tomography is superior to conventional imaging with (123)I-metaiodobenzylguanidine scintigraphy, computer tomography, and magnetic resonance imaging in localizing tumors causing catecholamine excess.

AbstractCONTEXT:
Catecholamine excess is rare, but symptoms may be life threatening.
OBJECTIVE:
The objective of the study was to investigate the sensitivity of 6-[F-18]fluoro-l-dihydroxyphenylalanine positron emission tomography ((18)F-DOPA PET), compared with (123)I-metaiodobenzylguanidine ((123)I-MIBG) scintigraphy and computer tomography (CT)/magnetic resonance imaging (MRI) for tumor localization in patients with catecholamine excess.
DESIGN AND SETTING:
All consecutive patients with catecholamine excess visiting the University Medical Center Groningen, Groningen, The Netherlands, between March 2003 and January 2008 were eligible.
PATIENTS:
Forty-eight patients were included. The final diagnosis was pheochromocytoma in 40, adrenal hyperplasia in two, paraganglioma in two, ganglioneuroma in one, and unknown in three.
MAIN OUTCOME MEASURES:
Sensitivities and discordancy between (18)F-DOPA PET, (123)I-MIBG, and CT or MRI were analyzed for individual patients and lesions. Metanephrines and 3-methoxytyramine in plasma and urine and uptake of (18)F-DOPA with PET were measured to determine the whole-body metabolic burden and correlated with biochemical tumor activity. The gold standard was a composite reference standard.
RESULTS:
(18)F-DOPA PET showed lesions in 43 patients, (123)I-MIBG in 31, and CT/MRI in 32. Patient-based sensitivity for (18)F-DOPA PET, (123)I-MIBG, and CT/MRI was 90, 65, and 67% (P < 0.01 for (18)F-DOPA PET vs. both (123)I-MIBG and CT/MRI, P = 1.0 (123)I-MIBG vs. CT/MRI). Lesion-based sensitivities were 73, 48, and 44% (P < 0.001 for (18)F-DOPA PET vs. both (123)I-MIBG and CT/MRI, P = 0.51 (123)I-MIBG vs. CT/MRI). The combination of (18)F-DOPA PET with CT/MRI was superior to (123)I-MIBG with CT/MRI (93 vs. 76%, P < 0.001). Whole-body metabolic burden measured with (18)F-DOPA PET correlated with plasma normetanephrine (r = 0.82), urinary normetanephrine (r = 0.84), and metanephrine (r = 0.57).
CONCLUSION:
To localize tumors causing catecholamine excess, (18)F-DOPA PET is superior to (123)I-MIBG scintigraphy and CT/MRI.
AuthorsHelle-Brit Fiebrich, Adrienne H Brouwers, Michiel N Kerstens, Milan E J Pijl, Ido P Kema, Johan R de Jong, Pieter L Jager, Philip H Elsinga, Rudi A J O Dierckx, Jacqueline E van der Wal, Wim J Sluiter, Elisabeth G E de Vries, Thera P Links
JournalThe Journal of clinical endocrinology and metabolism (J Clin Endocrinol Metab) Vol. 94 Issue 10 Pg. 3922-30 (Oct 2009) ISSN: 1945-7197 [Electronic] United States
PMID19622618 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Biomarkers
  • Catecholamines
  • Radiopharmaceuticals
  • fluorodopa F 18
  • 3-Iodobenzylguanidine
  • Dihydroxyphenylalanine
Topics
  • 3-Iodobenzylguanidine
  • Adolescent
  • Adrenal Gland Neoplasms (diagnosis, diagnostic imaging, metabolism)
  • Adrenal Glands (metabolism, pathology)
  • Adult
  • Aged
  • Biomarkers (metabolism)
  • Catecholamines (blood, metabolism, urine)
  • Child
  • Child, Preschool
  • Dihydroxyphenylalanine (analogs & derivatives)
  • Female
  • Humans
  • Hyperplasia (diagnosis)
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Paraganglioma (diagnosis, diagnostic imaging, metabolism)
  • Pheochromocytoma (diagnosis, diagnostic imaging, metabolism)
  • Positron-Emission Tomography (methods)
  • Prospective Studies
  • Radiopharmaceuticals
  • Sensitivity and Specificity
  • Tomography, X-Ray Computed
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: