Small target repeatability of 68 Ga and 18 F: effects of target concentration and imaging time on SUV measurements in clinically relevant phantoms

Quantification of tumor uptake using PET imaging is important for the evaluation of therapy response. For 18F FDG PET scans, a change in uptake of 25% is commonly considered significant. For scans using novel radiopharmaceuticals, the threshold of significance is unclear. Factors including imaging time, tumor size, activity concentration, and radiopharmaceutical may affect the repeatablity of uptake metrics. This work evaluates the effect of these parameters on the repeatablity of maximum SUV (SUVmax) and mean SUV (SUVmean) in phantoms using 18F and 68Ga. An Esser PET phantom (Data Spectrum, Durham NC) was scanned on a Biograph Horizon PET/CT scanner (Siemens Medical Solutions, Malvern PA) using 18F and 68Ga. Data were acquired for 5 minutes with reconstructions between 0.5-5 minutes. The background activity mimicked clinical scans with target-to-background (T/B) ratios from 1.7-19.8. The SUVmax and SUVmean were measured for 5 slices. The mean, standard deviation, and coefficient of variation (COV) were calculated. The effects of radionuclide, imaging time, activity concentration, and target size on COV were evaluated using multivariate gamma regressions. COV for 68Ga was 40% higher and 54% higher on average than for 18F for SUVmax and SUVmean, respectively. Decreased lesion size, imaging time, and activity concentration were significantly associated with increased COV for both metrics (P < 0.001). COV was substantially reduced at high T/B for 68Ga. At the highest T/B the COV for SUVmax and SUVmean was within the typical range seen for 18F. COV is relatively high for small targets (8 mm) but is dramatically reduced with high radiotracer uptake.