Concepedia

Publication | Open Access

<sup>64</sup>CuCl<sub>2</sub> PET/CT in Prostate Cancer Relapse

77

Citations

34

References

2017

Year

Abstract

Our objective was to evaluate the biodistribution, kinetics, and radiation dosimetry of <sup>64</sup>CuCl<sub>2</sub> in humans and to assess the ability of <sup>64</sup>CuCl<sub>2</sub> PET/CT to detect prostate cancer (PCa) recurrence in patients with biochemical relapse. <b>Methods:</b> We prospectively evaluated 50 PCa patients with biochemical relapse after surgery or external-beam radiation therapy. All patients underwent <sup>64</sup>CuCl<sub>2</sub> PET/CT, <sup>18</sup>F-choline PET/CT, and multiparametric MRI within 15 d of each other. Experienced readers interpreted the images, and the detection rate (DR) of each imaging modality was calculated. Histopathology, when available; clinical or laboratory response; and multidisciplinary follow-up were used to confirm the site of disease. In parallel, biodistribution, kinetics of the lesions, and radiation dosimetry of <sup>64</sup>CuCl<sub>2</sub> were evaluated. <b>Results:</b> From a dosimetric point of view, an administered dose of 200 MBq for <sup>64</sup>CuCl<sub>2</sub> translated into a 5.7-mSv effective dose. Unlike <sup>18</sup>F-choline, <sup>64</sup>CuCl<sub>2</sub> was not excreted or accumulated in the urinary tract, thus allowing thorough pelvic exploration. The maximum <sup>64</sup>CuCl<sub>2</sub> uptake at the sites of PCa relapse was observed 1 h after tracer injection. In our cohort, <sup>64</sup>CuCl<sub>2</sub> PET/CT proved positive in 41 of 50 patients, with an overall DR of 82%. The DRs of <sup>18</sup>F-choline PET/CT and multiparametric MRI were 56% and 74%, respectively. The difference between the DRs of <sup>64</sup>CuCl<sub>2</sub> PET/CT and <sup>18</sup>F-choline PET/CT was statistically significant (<i>P</i> < 0.001). Interestingly, on considering prostate-specific antigen (PSA) value, <sup>64</sup>CuCl<sub>2</sub> PET/CT had a higher DR than <sup>18</sup>F-choline PET/CT in patients with a PSA of less than 1 ng/mL. <b>Conclusion:</b> The biodistribution of <sup>64</sup>CuCl<sub>2</sub> is more suitable than that of <sup>18</sup>F-choline for exploring the pelvis and prostatic bed. The <sup>64</sup>CuCl<sub>2</sub> effective dose is like those of other established PET tracers. In patients with biochemical relapse and a low PSA level, <sup>64</sup>CuCl<sub>2</sub> PET/CT shows a significantly higher DR than <sup>18</sup>F-choline PET/CT.

References

YearCitations

Page 1