Abstract
A number of positron emission tomography (PET) radiotracers have been developed to improve the sensitivity and specificity of imaging for prostate cancer. These radiotracers include the bone-seeking agent Na18F as well as more tumor-specific compounds such as 11C-choline and 18F-fluciclovine. In this review, we will discuss the advantages and disadvantages of these PET radiotracers for the imaging of men with prostate cancer across a range of clinical contexts. We will also touch upon radiotracers in late clinical development that have not gained regulatory approval, including those targeted against prostate-specific membrane antigen (PSMA) and gastrin-releasing peptide receptor (GRPR).
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MGP is a co-inventor on a U.S. patent covering 18F-DCFPyL and as such is entitled to a portion of any licensing fees and royalties generated by this technology. This arrangement has been reviewed and approved by the Johns Hopkins University in accordance with its conflict-of-interest policies. SPR is a consultant to Progenics Pharmaceuticals, the licensee of 18F-DCFPyL. MAG has served as a consultant to Progenics Pharmaceuticals. SPR, MAG, and MGP receive research funding from Progenics Pharmaceuticals. There are no other potential conflicts of interest.
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Rowe, S.P., Johnson, G.B., Pomper, M.G. et al. Recent updates and developments in PET imaging of prostate cancer. Abdom Radiol 45, 4063–4072 (2020). https://doi.org/10.1007/s00261-020-02570-y
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DOI: https://doi.org/10.1007/s00261-020-02570-y