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. 2020 Jan-Mar;36(1):69–70. doi: 10.4103/iju.IJU_266_19

Table 1.

Various studies and agents/drugs in the treatment of mCRPC

Study Drug used Comparison Selection criterion OS in months PFS PSA reduction
COU-AA-302 Ryan CJ et al., 2013 Abiraterone + prednisone Placebo + prednisone No previous docetaxel
ECOG 0-1
PSA or radiographic progression
No or mild symptoms
No visceral metastases
34.7 versus 30.3 16.5 versus 8.3 >50% in 62%
PREVAIL Beer TM et al., 2014 Enzalutamide Placebo No previous docetaxel ECOG 0-1
PSA or radiographic progression
No or mild symptoms
10% had visceral metastases
32.4 versus 30.2 20.0 versus 5.4 >50% in 78%
Kantoff PW et al., 2010 Sipuleucel-T Placebo Some with previous docetaxel
ECOG 0-1
Asymptomatic or minimally symptomatic
25.8 versus 21.7 3.7 versus 3.6 >50% in 26%
Parker et al., 2013 Radium-223 Placebo Previous or no previous docetaxel
ECOG 0-2
Two or more symptomatic bone metastases
No visceral metastases
14.9 versus 11.3 NA >30% in 16%
deBono et al., 2010 Cabazitaxel + prednisone Mitoxantrone + prednisone Previous docetaxel
ECOG 0-2
15.1 versus 12.7 2.8 versus 1.4 NA
Kratochwil et al.[3] 225Ac-PSMA-617 chemotherapy naïve mCRPC >50% in 63%

mCRPC=Metastatic castrate resistant prostate cancer, PSA=Prostate-specific antigen, OS=Overall survival, PSMA=Prostate-specific membrane antigen, NA=Not available, ECOG=Eastern Cooperative Oncology Group