Limited value of fluorine-18 fluorodeoxyglucose positron emission tomography for the imaging of neuroendocrine tumours

• Published in: European journal of nuclear medicine Vol. 25; no. 1; pp. 79 - 83
• Main Authors: ADAMS, S, BAUM, R, RINK, T, SCHUMM-DRÄGER, P.-M, USADEL, K.-H, HÖR, G
• Format: Conference Proceeding Journal Article
• Language: English
• Published: Berlin Springer 01.01.1998; Springer Nature B.V
• Subjects: Adult; Aged; Biological and medical sciences; Cell cycle; Endocrine glands. Genital system. Mammary gland; Female; Fluorodeoxyglucose F18; Gastrointestinal Agents; Humans; Image Processing, Computer-Assisted; Investigative techniques, diagnostic techniques (general aspects); Male; Medical imaging; Medical research; Medical sciences; Middle Aged; Neuroendocrine Tumors - diagnostic imaging; Octreotide; Pancreatic Neoplasms - diagnostic imaging; Pentetic Acid; Radionuclide investigations; Radiopharmaceuticals; Stomach Neoplasms - diagnostic imaging; Technetium Tc 99m Dimercaptosuccinic Acid; Thyroid Neoplasms - diagnostic imaging; Tomography; Tomography, Emission-Computed; Tumors; Endocrinopathy; Radionuclide study; Human; Carcinoma; Neuroendocrinology; Thyroid diseases; Tumor; Thyroid gland; Somatostatin; Positron; Hormonal receptor; Emission tomography
• ISSN: 0340-6997; 1619-7070; 1619-7089
• DOI: 10.1007/s002590050197

Scintigraphy using [111In-DTPA-d-Phe1]-pentetreotide or pentavalent technetium-99m-dimercaptosuccinic acid [99mTc(V)-DMSA] has been shown to localize well-differentiated and slowly growing neuroendocrine tumours, whereas increased fluorodeoxyglucose (FDG) uptake is associated with malignancy. The aim of this study was to compare the value of fluorine-18 FDG positron emission tomography (PET) with that of somatostatin receptor scintigraphy (SS-R) and dual-radionuclide scintigraphy [SS-R and 99mTc(V)-DMSA = DNS] in detecting malignant neuroendocrine tumours. Fifteen patients with metastasizing gastroenteropancreatic tumours (GEP tumours; n = 7), medullary thyroid carcinomas (MTCs; n = 8) and elevated tumour markers [GEP tumours: 5-hydroxyindoleacetic acid, insulin; MTCs: calcitonin, carcinoembryonic antigen (CEA)] were studied. Prior to PET, all patients with GEP tumours underwent SS-R. DNS was performed in all patients with MTC. Patients had been fasting for at least 12 h and normal glucose plasma levels were confirmed. Sixty minutes after intravenous administration of 18F-FDG (mean: 374 MBq) whole-body PET and regional scans were performed. In addition, the resected tissues were prepared for immunocytochemistry examination (cell cycle-associated Ki-67 antigen). In two patients with less-differentiated GEP tumours associated with high proliferative activity and increased FDG uptake, SS-R failed to detect any lesion. In comparison, in four patients with well-differentiated GEP tumours showing low proliferative activity, SS-R localized four primary tumours, 22 lymph node metastases and 18 malignant liver lesions, whereas 18F-FDG PET demonstrated normal distribution. In one patient with a metastasizing carcinoid (medium proliferative activity) SS-R localized multiple metastases, whereas PET demonstrated low FDG uptake in all known metastases. In patients with recurrent MTC and rapidly increasing CEA levels DNS detected only three lesions in two patients, whereas PET demonstrated one pulmonary, three osseous, 20 mediastinal, ten locoregional, and four liver metastases in seven patients. Twenty-nine malignant lesions were confirmed by follow-up and nine lymph node metastases could be surgically removed. In conclusion, PET imaging of gastroenteropancreatic tumours revealed increased glucose metabolism only in less-differentiated GEP tumours with high proliferative activity and metastasizing MTC associated with rapidly increasing CEA levels. Therefore, additional 18F-FDG PET should be performed only if SS-R or DNS is negative.