Gallium-68 labeled somatostatin receptor antagonist PET/CT in over 500 patients with neuroendocrine neoplasms: experience from a single center in China.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 38337073.
- Also identified by DOI 10.1007/s00259-024-06639-4.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Somatostatin receptor antagonists have shown promising performance for imaging neuroendocrine neoplasms. However, there is a lack of studies exploring the diagnostic performance of SSTR antagonists or comparing them with agonists in a large cohort of patients with NENs. This study aimed to retrospectively review all SSTR antagonist PET/CT scans conducted at Peking Union Medical College Hospital since November 2018 in patients with confirmed or suspected NENs. Four types of SSTR antagonists were utilized, including [<sup>68</sup>Ga]Ga-NODAGA-LM3, [<sup>68</sup>Ga]Ga-DOTA-LM3, [<sup>68</sup>Ga]Ga-NODAGA-JR11, and [<sup>68</sup>Ga]Ga-DOTA-JR11. The reference standard was based on a combination of histopathology, clinical evaluation, imaging results, and follow-up. Patient-based sensitivity, specificity, and accuracy were evaluated. The SUV<sub>max</sub> and tumor-to-liver ratio (TLR) of the hottest lesions was recorded and compared between antagonists and [<sup>68</sup>Ga]Ga-DOTATATE. A total of 622 antagonist scans from 549 patients were included in the analysis. The patient-level sensitivity, specificity, and accuracy of antagonist imaging (all tracers combined) were 91.0% (443/487), 91.9% (57/62), and 91.1% (500/549), respectively. In 181 patients with a comparative [<sup>68</sup>Ga]Ga-DOTATATE PET/CT scan, the patient-level sensitivity, specificity, and accuracy were 87.5% (147/168), 76.9% (10/13), and 86.7% (157/181), respectively. For the hottest lesions, SSTR antagonists all tracers combined demonstrated an overall comparable SUV<sub>max</sub> to [<sup>68</sup>Ga]Ga-DOTATATE (40.1 ± 32.5 vs. 39.4 ± 23.8, p = 0.772). While [<sup>68</sup>Ga]Ga-NODAGA-LM3 showed significantly higher uptake than [<sup>68</sup>Ga]Ga-DOTATATE (57.4 ± 38.5 vs. 40.0 ± 22.8, p<0.001), [<sup>68</sup>Ga]Ga-NODAGA-JR11 (39.7 ± 26.5 vs. 34.3 ± 23.9, p = 0.108) and [<sup>68</sup>Ga]Ga-DOTA-LM3 (38.9 ± 32.1 vs. 37.2 ± 22.1, p = 0.858) showed comparable uptake to [<sup>68</sup>Ga]Ga-DOTATATE, and [<sup>68</sup>Ga]Ga-DOTA-JR11 showed lower uptake (28.9 ± 26.1 vs. 44.0 ± 25.7, p = 0.001). All antagonists exhibited significantly higher TLR than [<sup>68</sup>Ga]Ga-DOTATATE (12.1 ± 10.8 vs. 5.2 ± 4.5, p<0.001). Gallium-68 labeled SSTR antagonists could serve as alternatives to SSTR agonists for imaging of NENs. Among various antagonists, [<sup>68</sup>Ga]Ga-NODAGA-LM3 seems to have the best imaging profile.
Medical subject headings
- Positron Emission Tomography Computed Tomography
- Receptors, Somatostatin
- Neuroendocrine Tumors
- Gallium Radioisotopes