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1 y (docetaxel), abiraterone, enzalutamide, or radium 223.
2 MPCA study and before regulatory approval of radium-223.
3 docetaxel use on the efficacy and safety of radium-223.
4 s performed before crossover from placebo to radium-223.
5 cetaxel, cabazitaxel), radiopharmaceuticals (radium 223, (177)Lu-prostate-specific membrane antigen [
7 ing exposure to alpha-particles emitted from radium-223 ((223)Ra) using 28 genetically diverse human
9 terone acetate/prednisone, enzalutamide, and radium-223 ((223)Ra; for men with predominantly bone met
10 696 patients received one or more doses of radium-223; 403 (58%) of these patients had all six plan
11 response system to receive six injections of radium-223 (50 kBq/kg intravenously) or matching placebo
12 receive either six intravenous injections of radium-223 (50 kBq/kg) or matching placebo; one injectio
13 Patients received intravenous injections of radium-223, 50 kBq/kg (current recommendation 55 kBq/kg
14 receive up to six intravenous injections of radium-223 (55 kBq/kg) or matching placebo once every 4
15 PCA trial showed that radium-223 dichloride (radium-223), a targeted alpha-emitter, improved overall
19 mia and neutropenia were similar between the radium-223 and placebo groups within both docetaxel subg
21 azitaxel, abiraterone acetate, enzalutamide, radium-223, and sipuleucel-T has increased the number of
22 amide, darolutamide, docetaxel, cabazitaxel, radium-223, and sipuleucel-T have been approved for adva
24 terim analysis, which involved 809 patients, radium-223, as compared with placebo, significantly impr
25 in a 2:1 ratio, to receive six injections of radium-223 (at a dose of 50 kBq per kilogram of body wei
30 hypothesized the BM-targeting alpha-emitter radium-223 dichloride (Ra223) could target subclinical b
32 ignificantly longer in patients treated with radium-223 dichloride (radium-223) than in patients trea
33 from the phase 3 ALSYMPCA trial showed that radium-223 dichloride (radium-223), a targeted alpha-emi
35 ncreasing with the adoption into practice of radium-223 dichloride for the treatment of bone metastas
36 itionally, the radioactive therapeutic agent radium-223 dichloride has been recently approved in pati
40 deaths occurred in two (1%) patients in the radium-223 group (acute myocardial infarction and inters
41 occurred in 202 (33%) of 614 patients in the radium-223 group and 116 (38%) of 307 patients in the pl
43 events occurred in 160 (41%) patients in the radium-223 group and 155 (39%) in the placebo group.
44 ved previous docetaxel treatment (352 in the radium-223 group and 174 in the placebo group) and 395 (
45 al was 22.3 months (95% CI 20.4-24.8) in the radium-223 group and 26.0 months (21.8-28.3) in the plac
46 occurred in 112 (29%) of 392 patients in the radium-223 group and 45 (11%) of 394 patients in the pla
47 Feb 15, 2018), 196 (49%) of 401 patients in radium-223 group had had at least one symptomatic skelet
48 more fractures and deaths were noted in the radium-223 group than in the placebo group (in an unplan
49 were hypertension (43 [11%] patients in the radium-223 group vs 52 [13%] patients in the placebo gro
56 ated events, whereas the radiopharmaceutical radium-223 is shown to reduce the incidence of symptomat
57 .1%] with some postsecondary education), and radium 223 (n = 21) (mean [SD] age, 76.4 [7.2] years; 17
58 6 patients were randomly assigned to receive radium-223 (n=401) or placebo (n=405) in addition to abi
61 val was also longer in patients who received radium-223 plus abiraterone, enzalutamide, or both (medi
62 months, 12-16), and in patients who received radium-223 plus denosumab (median NA, 15 months-NA) than
64 of enzalutamide and 6 monthly injections of radium-223 (Ra223) in patients with metastatic castratio
68 nalysis involving 921 patients confirmed the radium-223 survival benefit (median, 14.9 months vs. 11.
69 incidence of grade 3-4 thrombocytopenia with radium-223 than with placebo (31 [9%] of 347 patients vs
70 t symptomatic skeletal event was longer with radium-223 than with placebo (median 15.6 months [95% CI
73 investigated safety and overall survival in radium-223 treated patients in an early access programme
75 ated the effect of previous docetaxel use on radium-223 treatment for the primary endpoint of overall
76 symptomatic skeletal event was reduced with radium-223 versus placebo in patients with previous doce
79 , enzalutamide, or radium Ra 223 dichloride (radium 223) were enrolled between July 1, 2015, and Dece
80 15 months-NA) than in patients who received radium-223 without denosumab (median 13 months, 12-NA).