Head-to-Head Comparison of ¹¹C-PBR28 and ¹⁸F-GE180 for Quantification of the Translocator Protein in the Human Brain.

Abstract

¹⁸F-GE180 is a third-generation PET tracer for quantifying the translocator protein (TSPO), a biomarker for inflammation. The aim of this study was to perform a head-to-head comparison of ¹⁸F-GE180 and the well-established TSPO tracer ¹¹C-PBR28 by scanning with both tracers during the same day in the same subjects. <b>Methods:</b> Five subjects underwent a 90-min PET scan with ¹¹C-PBR28 in the morning and ¹⁸F-GE180 in the afternoon. A metabolite-corrected arterial input function was obtained in each subject for both tracers, and the brain uptake was quantified with a 2-tissue-compartment model. <b>Results:</b> The rate of metabolism of ¹⁸F-GE180 in arterial blood was slower than that of ¹¹C-PBR28 (the percentages of nonmetabolized parent in plasma at 90 min were 74.9% ± 4.15% [mean ± SD] and 11.2% ± 1.90%, respectively). The plasma free fractions were similar for both tracers: 3.5% ± 1.1% for ¹⁸F-GE180 and 4.1% ± 1.1% for ¹¹C-PBR28. The average total volume of distribution (<i>V</i>_T) of ¹⁸F-GE180 was about 20 times smaller than that of ¹¹C-PBR28 (0.15 ± 0.03 mL/cm³ for ¹⁸F-GE180 and 3.27 ± 0.66 mL/cm³ for ¹¹C-PBR28). ¹⁸F-GE180 was characterized by poor transfer from the vascular compartment to the brain (its plasma-to-tissue rate constant [K₁] was about 10 times smaller than that of ¹¹C-PBR28). Moreover, kinetic modeling was more difficult with ¹⁸F-GE180, as its <i>V</i>_T values were identified with a lower precision than those of ¹¹C-PBR28 and outlying values were more frequent. <b>Conclusion:</b> The <i>V</i>_T of ¹⁸F-GE180 was about 20 times smaller than that of ¹¹C-PBR28 because of low penetration into the brain from the vascular compartment. In addition, kinetic modeling of ¹⁸F-GE180 was more challenging than that of ¹¹C-PBR28. Therefore, compared with ¹¹C-PBR28, ¹⁸F-GE180 had unfavorable characteristics for TSPO imaging of the brain.