Comparison of <sup>68</sup>Ga-DOTA-JR11 PET/CT with dosimetric <sup>177</sup>Lu-satoreotide tetraxetan (<sup>177</sup>Lu-DOTA-JR11) SPECT/CT in patients with metastatic neuroendocrine tumors undergoing peptide receptor radionuclide therapy.

Krebs, Simone; O'Donoghue, Joseph A; Biegel, Evan; Beattie, Bradley J; Reidy, Diane; Lyashchenko, Serge K; Lewis, Jason S; Bodei, Lisa et al. · Eur J Nucl Med Mol Imaging · 2020

prospective_cohort · Level II

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Abstract

Paired imaging/therapy with radiolabeled somatostatin receptor (SSTR) antagonists is a novel approach in neuroendocrine tumors (NETs). The aim of this study was to compare tumor uptake of <sup>68</sup>Ga-DOTA-JR11 and <sup>177</sup>Lu-satoreotide tetraxetan (<sup>177</sup>Lu-DOTA-JR11) in patients with NETs. As part of a prospective clinical trial, 20 patients with metastatic NETs underwent <sup>68</sup>Ga-DOTA-JR11 PET/CT and serial imaging with <sup>177</sup>Lu-satoreotide tetraxetan. PET/CT and SPECT/CT parameters for lesion uptake and absorbed dose of <sup>177</sup>Lu-satoreotide tetraxetan in lesions were compared using linear regression analysis and Pearson correlation. A total of 95 lesions were analyzed on <sup>68</sup>Ga-DOTA-JR11 PET/CT and <sup>177</sup>Lu-satoreotide tetraxetan SPECT/CT. SUVs and tumor-to-normal-tissue ratios on PET/CT and SPECT/CT were significantly correlated (p < 0.01), but the degree of correlation was modest with Pearson correlation coefficients ranging from 0.3 to 0.7. Variation in intrapatient lesional correlation was observed. Nevertheless, in all patients, the lesion SUVpeak uptake ratio for <sup>177</sup>Lu-satoreotide tetraxetan vs. <sup>68</sup>Ga-DOTA-JR11 was high; even in those with low uptake on <sup>68</sup>Ga-DOTA-JR11 PET/CT (SUVpeak ≤ 10), a ratio of 8.0 ± 5.2 was noted. Correlation of SUVpeak of <sup>68</sup>Ga-DOTA-JR11 with projected <sup>177</sup>Lu-satoreotide tetratexan-absorbed dose (n = 42) was modest (r = 0.5, p < 0.01), while excellent correlation of SUVpeak of <sup>177</sup>Lu-satoreotide tetraxetan with projected <sup>177</sup>Lu-satoreotide tetraxetan-absorbed dose was noted (r = 0.9, p < 0.0001). Our study shows that <sup>68</sup>Ga-DOTA-JR11 PET can be used for patient selection and PRRT and that low tumor uptake on PET should not preclude patients from treatment with <sup>177</sup>Lu-satoreotide tetraxetan. The ability to use single time-point SPECT/CT for absorbed dose calculations could facilitate dosimetry regimens, save costs, and improve patient convenience.

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