Evaluation of [<sup>68</sup>Ga]Ga-DATA-TOC for imaging of neuroendocrine tumours: comparison with [<sup>68</sup>Ga]Ga-DOTA-NOC PET/CT.
prospective_cohort · Level II
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- Record sourced from PubMed, PMID 31754796.
- Also identified by DOI 10.1007/s00259-019-04611-1.
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Abstract
Recently, the new hybrid chelator DATA (6-amino-1,4-diazepine-triacetate) has been introduced, which has the advantage of high yield and radiolabelling of DATA-based octreotide derivative (TOC) at room temperature in contrast to tetraazacyclododecane-1,4,7,10-tetraacetate (DOTA) that needs 95 °C for effective labelling. However, the diagnostic potential of DATA-TOC has not been studied with other chelators in humans. The aim of this study was to compare the diagnostic efficacy of [<sup>68</sup>Ga]Ga-DATA-TOC with [<sup>68</sup>Ga]Ga-DOTA-NOC (which is the current standard for imaging neuroendocrine tumours (NET)) in patients of gastroenteropancreatic neuroendocrine tumours (GEP-NETs). Fifty patients (thirty-one males and nineteen females) with biopsy-proven GEP-NETs were included in the study. Patients age ranged from 14 to 75 years (mean 46.11 years). All patients underwent two PET studies with [<sup>68</sup>Ga]Ga-DATA-TOC and [<sup>68</sup>Ga]Ga-DOTA-NOC. Images were evaluated visually and semi-quantitatively using maximum standardized uptake values (SUVmax) of tumour, mediastinum and liver. Tumour-to-liver (T/L) and tumour-to-mediastinum (T/M) SUVmax ratios were computed. For the purpose of comparison, patient-wise as well as lesion-wise analysis was carried out. The nonparametric-related samples Wilcoxon signed-rank test was used for comparison of the SUVmax values and ratios. On visual evaluation, the biodistribution and image quality of [<sup>68</sup>Ga]Ga-DATA-TOC was similar to [<sup>68</sup>Ga]Ga-DOTA-NOC. Physiological liver uptake was lower in [<sup>68</sup>Ga]Ga-DATA-TOC as compared with [<sup>68</sup>Ga]Ga-DOTA-NOC, 7.65 ± 5.37 vs 8.94 ± 5.95 (p = 0.009), respectively. On a patient-wise analysis, both [<sup>68</sup>Ga]Ga-DATA-TOC and [<sup>68</sup>Ga]Ga-DOTA-NOC were lesion-positive in the 44 patients (88%) and were negative in the 6 patients (12%). On a lesion-based analysis, [<sup>68</sup>Ga]Ga-DATA-TOC had 98.6% concordance with [<sup>68</sup>Ga]Ga-DOTA-NOC (232 out of 235 lesions detected). The target tumour SUVmax on [<sup>68</sup>Ga]Ga-DATA-TOC and [<sup>68</sup>Ga]Ga-DOTA-NOC were 36.63 ± 32.24 and 40.82 ± 36.89, respectively (p = 0.097). The T/L SUVmax ratios were not significantly different (5.99 ± 5.52 vs 5.67 ± 4.96, p = 0.77). [<sup>68</sup>Ga]Ga-DATA-TOC PET/CT imaging produced results that were comparable with [<sup>68</sup>Ga]Ga-DOTA-NOC. It, thus, has potential utility as an effective and safe alternative to <sup>68</sup>Ga-DOTA-NOC with the added benefit of ease, cost-effective and improved yield of instant kit-type synthesis.
Medical subject headings
- Neuroendocrine Tumors
- Organometallic Compounds