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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.
- Source :
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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
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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