4.4 Article

Biodistribution of 18F-AlF-NOTA-octreotide in Different Organs and Characterization of Uptake in Neuroendocrine Neoplasms

Journal

MOLECULAR IMAGING AND BIOLOGY
Volume 23, Issue 6, Pages 827-835

Publisher

SPRINGER
DOI: 10.1007/s11307-021-01628-7

Keywords

Neuroendocrine neoplasm; F-18-AlF-NOTA-octreotide; PET/CT; Biodistribution

Funding

  1. National Natural Science Foundation of China [91859207, 81771873, 81471689]

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This study aimed to describe the biodistribution of F-18-OC in normal organs, evaluate the uptake range of NEN and benign lesions, and compare the differences in F-18-OC uptake among tumors of different grades. The results showed varying levels of uptake in different organs, differences between NENs and benign lesions, and variations in uptake levels among NENs of different grades.
Purpose: The aims of this study were threefold: [1] to describe the biodistribution of F-18-AlF-NOTA-octreotide (F-18-OC) in normal organs; [2] to evaluate the range of uptake of NEN and benign lesions using the maximum standardized uptake value (SUVmax); and [3] to compare the difference in F-18-OC uptake among tumors of different grades. Methods: This study included 162 patients (67 females and 95 males) who received F-18-OC positron emission tomography (PET)/computed tomography (CT), 128 of whom were diagnosed with neuroendocrine neoplasms (NENs). The SUVmax and SUVmean of F-18-OC were measured in 21 normal anatomical structures. We compared the differences among G1, G2, and G3 NENs, as well as between NENs and benign lesions. Results: High physiological uptake of F-18-OC (SUVmax > 6.77) was detected in the spleen, adrenal gland, renal parenchyma, pituitary gland, and liver. Moderate uptake (SUVmax 3.00-6.77) was found in the uncinate process of the pancreas (PU), prostate, thyroid, and uterus. Mild uptake (SUVmax 1.34-3.00) was observed in the small intestine, pancreas (pancreas uptake except for the head of the pancreas), gallbladder, and transverse colon. The SUVmax of NENs was higher than that of benign lesions, including fractures, inflamed tissue, reactive hyperplasia, and degenerative disease. However, overlap was noted between the two groups. The SUVmax of F-18-OC uptake by tumors was significantly correlated with tumor grade in primary lesions and those of the lymph node, bone, and other sites (all P < 0.01). Conclusions: The results obtained from the majority of the samples in this study show the biodistribution of F-18-OC in normal organs and have significance as a reference. Although some benign lesions show variable uptake, the uptake by these lesions is still different from that of NENs. NENs of different grades have differences in F-18-OC uptake levels.

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