Identification of a PET Radiotracer for Imaging of the Folate Receptor-α: A Potential Tool to Select Patients for Targeted Tumor Therapy.

Abstract

The aim of this study was to identify a folate receptor-α (FRα)-selective PET agent potentially suitable for the selection of patients who might profit from FRα-targeted therapies. The 6<i>R</i> and 6<i>S</i> isomers of ¹⁸F-aza-5-methyltetrahydrofolate (MTHF) were assessed regarding their binding to FRα and FRβ, expressed on cancer and inflammatory cells, respectively, and compared with ¹⁸F-AzaFol, the folic acid-based analog. <b>Methods:</b> FR selectivity was investigated using FRα-transfected (RT16) and FRβ-transfected (D4) CHO cells. The cell uptake of ¹⁸F-folate tracers was investigated, and receptor-binding affinities were determined with the nonradioactive analogs. In vitro autoradiography of the ¹⁸F-folate tracers was performed using RT16 and D4 tissue sections. Biodistribution studies and PET/CT imaging of the radiotracers were performed on mice bearing RT16 and D4 xenografts. <b>Results:</b> The uptake of ¹⁸F-6<i>R</i>-aza-5-MTHF was high when using RT16 cells (62% ± 10% of added activity) but much lower when using D4 cells (5% ± 2%). The FRα selectivity of ¹⁸F-6<i>R</i>-aza-5-MTHF was further demonstrated by its approximately 43-fold higher binding affinity to FRα (half-maximal inhibitory concentration [IC₅₀], 1.8 ± 0.1 nM) than to FRβ (IC₅₀, 77 ± 27 nM). The uptake of ¹⁸F-6<i>S</i>-aza-5-MTHF and ¹⁸F-AzaFol was equal in both cell lines (52%-70%), with similar affinities to FRα (IC₅₀, 2.1 ± 0.4 nM and 0.6 ± 0.3 nM, respectively) and FRβ (0.8 ± 0.2 nM and 0.3 ± 0.1 nM, respectively). The autoradiography signal obtained with ¹⁸F-6<i>R</i>-aza-5-MTHF was 11-fold more intense for RT16 than for D4 tissue sections. Biodistribution data showed high uptake of ¹⁸F-6<i>R</i>-aza-5-MTHF in RT16 xenografts (81% ± 20% injected activity per gram [IA]/g 1 h after injection) but significantly lower accumulation in D4 xenografts (7.3% ± 2.1% IA/g 1 h after injection), which was also visualized using PET. The uptake of ¹⁸F-6<i>S</i>-aza-5-MTHF and ¹⁸F-AzaFol was similar in RT16 (53% ± 10% IA/g and 45% ± 2% IA/g, respectively) and D4 xenografts (77% ± 10% IA/g and 52% ± 7% IA/g, respectively). <b>Conclusion:</b> This study demonstrated FRα selectivity for ¹⁸F-6<i>R</i>-aza-5-MTHF but not for ¹⁸F-6<i>S</i>-aza-5-MTHF or ¹⁸F-AzaFol. This characteristic, together with its favorable tissue distribution, makes ¹⁸F-6<i>R</i>-aza-5-MTHF attractive for clinical translation to enable detection of FRα-positive cancer while preventing undesired accumulation in FRβ-expressing inflammatory cells.