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Somatostatin Receptor Imaging with [ 18 F]FET-βAG-TOCA PET/CT and [ 68 Ga]Ga-DOTA-Peptide PET/CT in Patients with Neuroendocrine Tumors: A Prospective, Phase 2 Comparative Study.

Authors :
Dubash S
Barwick TD
Kozlowski K
Rockall AG
Khan S
Khan S
Yusuf S
Lamarca A
Valle JW
Hubner RA
McNamara MG
Frilling A
Tan T
Wernig F
Todd J
Meeran K
Pratap B
Azeem S
Huiban M
Keat N
Lozano-Kuehne JP
Aboagye EO
Sharma R
Source :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2024 Feb 08. Date of Electronic Publication: 2024 Feb 08.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

There is a clinical need for <superscript>18</superscript> F-labeled somatostatin analogs for the imaging of neuroendocrine tumors (NET), given the limitations of using [ <superscript>68</superscript> Ga]Ga-DOTA-peptides, particularly with regard to widespread accessibility. We have shown that [ <superscript>18</superscript> F]fluoroethyl-triazole-[Tyr <superscript>3</superscript> ]-octreotate ([ <superscript>18</superscript> F]FET-βAG-TOCA) has favorable dosimetry and biodistribution. As a step toward clinical implementation, we conducted a prospective, noninferiority study of [ <superscript>18</superscript> F]FET-βAG-TOCA PET/CT compared with [ <superscript>68</superscript> Ga]Ga-DOTA- peptide PET/CT in patients with NET. Methods: Forty-five patients with histologically confirmed NET, grades 1 and 2, underwent PET/CT imaging with both [ <superscript>18</superscript> F]FET-βAG-TOCA and [ <superscript>68</superscript> Ga]Ga-peptide performed within a 6-mo window (median, 77 d; range, 6-180 d). Whole-body PET/CT was conducted 50 min after injection of 165 MBq of [ <superscript>18</superscript> F]FET-βAG-TOCA. Tracer uptake was evaluated by comparing SUV <subscript>max</subscript> and tumor-to-background ratios at both lesion and regional levels by 2 unblinded, experienced readers. A randomized, blinded reading of both scans was also then undertaken by 3 experienced readers, and consensus was assessed at a regional level. The ability of both tracers to visualize liver metastases was also assessed. Results: A total of 285 lesions were detected on both imaging modalities. An additional 13 tumor deposits were seen in 8 patients on [ <superscript>18</superscript> F]FET-βAG-TOCA PET/CT, and [ <superscript>68</superscript> Ga]Ga-DOTA-peptide PET/CT detected an additional 7 lesions in 5 patients. Excellent correlation in SUV <subscript>max</subscript> was observed between both tracers ( r = 0.91; P < 0.001). No difference was observed between median SUV <subscript>max</subscript> across regions, except in the liver, where the median tumor-to-background ratio of [ <superscript>18</superscript> F]FET-βAG-TOCA was significantly lower than that of [ <superscript>68</superscript> Ga]Ga-DOTA-peptide (2.5 ± 1.9 vs. 3.5 ± 2.3; P < 0.001). Conclusion: [ <superscript>18</superscript> F]FET-βAG-TOCA was not inferior to [ <superscript>68</superscript> Ga]Ga-DOTA-peptide in visualizing NET and may be considered in routine clinical practice given the longer half-life and availability of the cyclotron-produced fluorine radioisotope.<br /> (© 2024 by the Society of Nuclear Medicine and Molecular Imaging.)

Details

Language :
English
ISSN :
1535-5667
Database :
MEDLINE
Journal :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Publication Type :
Academic Journal
Accession number :
38331457
Full Text :
https://doi.org/10.2967/jnumed.123.266601