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Bone-Targeted Imaging and Radionuclide Therapy in Prostate Cancer JOURNAL OF NUCLEAR MEDICINE Iagaru, A. H., Mittra, E., Colletti, P. M., Jadvar, H. 2016; 57: 19S-24S

Abstract

Although selective metabolic and receptor-based molecular agents will surely be included in the future of prostate cancer diagnosis and therapy, currently available inorganic compounds-such as (18)F-NaF for the diagnosis of bony disease and (223)RaCl2 for the therapy of bone metastases-were recently shown to be superior to standard (99m)Tc-phosphonates for diagnosis and (153)Sm-ethylenediaminetetramethylene phosphonate or (89)SrCl2 for therapy. The advantages of (18)F-NaF include improved lesion detection and, when used in combination with CT, improved diagnostic confidence and specificity. In addition to being the first approved a-emitter, (223)RaCl2 is the first radiopharmaceutical to show an increase in overall survival, a decrease in skeletal events, palliation of bone pain, and a low profile of adverse reactions (which are mild and manageable). The management of metastatic bone disease with (223)RaCl2 is uniquely satisfying, as patients can be monitored directly during their monthly treatment visits.

View details for DOI 10.2967/jnumed.115.170746

View details for Web of Science ID 000384962100005

View details for PubMedID 27694165