Gallium-68 labeled somatostatin receptor antagonist PET/CT in over 500 patients with neuroendocrine neoplasms: experience from a single center in China.

Liu, Meixi; Cheng, Yuejuan; Bai, Chunmei; Zhao, Hong; Jia, Ru; Chen, Jingci; Zhu, Wenjia; Huo, Li · Eur J Nucl Med Mol Imaging · 2024

retrospective_cohort · Level III

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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.

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