The Influence of Specific Activity on the Biodistribution of <sup>18</sup>F-rhPSMA-7.3: A Retrospective Analysis of Clinical PET Data.
retrospective_cohort · Level III
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- Record sourced from PubMed, PMID 34385338.
- Also identified by DOI 10.2967/jnumed.121.262471.
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Abstract
We investigated whether the time between synthesis and injection and the resulting decrease in specific activity affects the normal-organ and tumor uptake of the PSMA ligand <sup>18</sup>F-rhPSMA-7.3 in patients with prostate cancer. <b>Methods:</b> The biodistribution of <sup>18</sup>F-rhPSMA-7.3 on PET/CT scans obtained with a high specific activity (median, 178.9 MBq/µg; <i>n</i> = 42) and a low specific activity (median, 19.3 MBq/µg; <i>n</i> = 42) was compared. <b>Results:</b> Tracer uptake by the parotid gland, submandibular gland, and spleen was moderately but significantly lower in the low-specific-activity group than in the high-specific-activity group (median SUV<sub>mean</sub>, 16.7 vs. 19.2; 18.1 vs. 22.3; and 7.8 vs. 9.6, respectively). No other statistically significant differences were found for normal organs or tumor lesions. <b>Conclusion:</b> A 10-fold decrease in specific activity has only minor effects on the biodistribution of <sup>18</sup>F-rhPSMA-7.3. These findings suggest that <sup>18</sup>F-labeled PSMA ligands can be centrally produced and shipped to PET clinics in a similar way to <sup>18</sup>F-FDG.
Medical subject headings
- Positron Emission Tomography Computed Tomography
- Prostatic Neoplasms