Publication | Open Access
Head-to-Head Comparison of <sup>64</sup>Cu-DOTATATE and <sup>68</sup>Ga-DOTATOC PET/CT: A Prospective Study of 59 Patients with Neuroendocrine Tumors
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References
2016
Year
Somatostatin receptor imaging is a valuable tool in the diagnosis, follow-up, and treatment planning of neuroendocrine tumor (NET). PET-based tracers using <sup>68</sup>Ga as the radioisotope have in most centers replaced SPECT-based tracers as the gold standard. <sup>64</sup>Cu-DOTATATE is a new PET tracer that has been shown to be far superior to the SPECT tracer <sup>111</sup>In-diethylenetriaminepentaacetic acid-octreotide. Because of the advantages of <sup>64</sup>Cu over <sup>68</sup>Ga, we hypothesized that the tracer has a higher sensitivity than <sup>68</sup>Ga-based tracers. To test this hypothesis, we compared on a head-to-head basis the diagnostic performance of <sup>64</sup>Cu-DOTATATE with that of <sup>68</sup>Ga-DOTATOC in NET patients. <b>Methods:</b> Fifty-nine NET patients were scanned with both <sup>64</sup>Cu-DOTATATE and <sup>68</sup>Ga-DOTATOC PET/CT and compared on a head-to-head basis. Discordant lesions were verified during at least 30 mo of follow-up. <b>Results:</b> A total of 701 lesions were concordantly detected on both <sup>64</sup>Cu-DOTATATE and <sup>68</sup>Ga-DOTATOC PET/CT scans, whereas an additional 68 lesions were found by only one of the scans. <sup>64</sup>Cu-DOTATATE showed 42 lesions not found on <sup>68</sup>Ga-DOTATOC, of which 33 were found to be true-positive on follow-up. <sup>68</sup>Ga-DOTATOC showed 26 lesions not found on <sup>64</sup>Cu-DOTATATE, of which 7 were found to be true-positive on follow-up. False-positives were mainly lymph node lesions. Accordingly, 83% of the additional true lesions found on only one of the scans were found by <sup>64</sup>Cu-DOTATATE. On a patient-basis, additional true lesions were found by <sup>64</sup>Cu-DOTATATE and <sup>68</sup>Ga-DOTATOC in 13 and 3 patients, respectively. All patients with additional lesions also had concordant lesions found by both scans. <b>Conclusion:</b><sup>64</sup>Cu-DOTATATE has advantages over <sup>68</sup>Ga-DOTATOC in the detection of lesions in NET patients. Although patient-based sensitivity was the same for <sup>64</sup>Cu-DOTATATE and <sup>68</sup>Ga-DOTATOC in this cohort, significantly more lesions were detected by <sup>64</sup>Cu-DOTATATE. Furthermore, the shelf life of more than 24 h and the scanning window of at least 3 h make <sup>64</sup>Cu-DOTATATE favorable and easy to use in the clinical setting.
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