Abstract
Although positron emission tomography (PET) imaging with 18-Fluorodeoxyglucose ((18)F-FDG) is a promising technique in multiple myeloma (MM), the development of other radiopharmaceuticals seems relevant. CD138 is currently used as a standard marker for the identification of myeloma cells and could be used in phenotype tumor imaging. In this study, we used an anti-CD138 murine antibody (9E7.4) radiolabeled with copper-64 ((64)Cu) or zirconium-89 ((89)Zr) and compared them in a syngeneic mouse model to select the optimal tracers for MM PET imaging. Then, 9E7.4 was conjugated to TE2A-benzyl isothiocyanate (TE2A) and desferrioxamine (DFO) chelators for (64)Cu and (89)Zr labeling, respectively. (64)Cu-TE2A-9E7.4 and (89)Zr-DFO-9E7.4 antibodies were evaluated by PET imaging and biodistribution studies in C57BL/KaLwRij mice bearing either 5T33-MM subcutaneous tumors or bone lesions and were compared to (18)F-FDG-PET imaging. In biodistribution and PET studies, (64)Cu-TE2A-9E7.4 and (89)Zr-DFO-9E7.4 displayed comparable good tumor uptake of subcutaneous tumors. On the bone lesions, PET imaging with (64)Cu-TE2A-9E7.4 and (89)Zr-DFO-9E7.4 showed higher uptake than with (18)F-FDG-PET. Comparison of both 9E7.4 conjugates revealed higher nonspecific bone uptakes of (89)Zr-DFO-9E7.4 than (64)Cu-TE2A-9E7.4. Because of free (89)Zr's tropism for bone when using (89)Zr-anti-CD138, (64)Cu-anti-CD138 antibody had the most optimal tumor-to-nontarget tissue ratios for translation into humans as a specific new imaging radiopharmaceutical agent in MM.