Bone is the most common site of
metastasis in metastatic
castration-resistant
prostate cancer (mCRPC), which is associated with
pain and skeletal events.
Radium-223 dichloride (
Xofigo) is an alpha-emitting
radioactive isotope that can specifically target bone lesions. Herein, we report the results of a retrospective analysis that documents our experience in the use of
radium-223. Data from 63 patients (pts) with mCRPC who underwent
radium-223 treatment from December 2015 to September 2017 were collected.
Radium-223 (55 kBq/kg) was administered every 4 weeks for up to 6 cycles. The primary endpoint was OS.
Radium-223 was administered as first line
therapy in 11 pts, as second line in 19 pts, as third line in 16 pts and in successive lines in 17 pts; 42 pts out of 63 (67%) completed all six cycles. Within one month after the end of 6 cycles of
radium-223, 15 pts out of 42 (35.7%) had achieved PR, 11 pts out of 42 (26.2%) had SD and 14 pts out of 42 (33.3%) had PD. Levels of
pain decreased with progressive cycles of
radium-223. After a minimum follow-up of 2 months and a maximum of 43 months, median OS was 15 months and median PFS was 8 months. The most frequent
radium-223 related toxicity was low grade haematologic toxicity, predominantly G1-G2, that occurred halfway through treatment in about 75% of pts. The favourable results reported herein confirm that
radium-223 can be considered well tolerated and effective in mCRPC, and is associated with significant decreases in
pain.