TY - JOUR
T1 - Outcomes with abiraterone acetate in metastatic castration-resistant prostate cancer patients who have poor performance status
AU - Azad, Arun A.
AU - Eigl, Bernhard J.
AU - Leibowitz-Amit, Raya
AU - Lester, Renee
AU - Kollmannsberger, Christian
AU - Murray, Nevin
AU - Clayton, Ravinder
AU - Heng, Daniel Y.C.
AU - Joshua, Anthony M.
AU - Chi, Kim N.
N1 - Funding Information:
Financial disclosures: Kim N. Chi certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Dr Chi received research funding from OncoGenex Technologies Inc., Astellas, Janssen, and Novartis and is a consultant for Janssen, Astellas, Amgen, Bayer, Millennium, Novartis, and Sanofi. Dr Eigl received an unrestricted educational grant from Janssen. Dr Azad received research funding from Astellas. Dr Joshua received research funding from Janssen-Ortho.
PY - 2015/3/1
Y1 - 2015/3/1
N2 - Background Although abiraterone acetate (abiraterone) has proven efficacy in two randomised phase 3 trials in metastatic castration-resistant prostate cancer (mCRPC), patients who had an Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤2 were either excluded or under-represented in these trials. Objective To compare outcomes in ECOG PS 0-1 and ≤2 in mCRPC patients treated with abiraterone. Design, setting, and participants Cancer registries from three Canadian centres were used to retrospectively identify mCRPC patients (postdocetaxel and docetaxel-naïve) treated with abiraterone. ECOG PS, clinicopathologic characteristics, prostate-specific antigen (PSA) response, and survival data were collected. Outcome measurements and statistical analysis Survival outcomes were estimated using the Kaplan-Meier method and compared using the log-rank test. Cox proportional hazards modelling was used to examine the effect of clinicopathologic characteristics on overall survival (OS) and time to PSA progression. Results and limitations A total of 519 patients were identified; 61% (n = 318) and 39% (n = 201) were ECOG PS 0-1 and ≤2, respectively. ECOG PS 0-1 patients were significantly more likely than PS ≤2 patients to achieve a PSA decline ≤50% from baseline (45% vs 32%; p = 0.003, Fisher exact test) and had significantly longer median time to PSA progression (5.2 mo vs 4.1 mo; p = 0.023), median treatment duration (7.4 mo vs 4.5 mo; p < 0.001), and median OS (20.0 mo vs 9.1 mo; p < 0.001). On multivariate analysis, ECOG PS was a significant factor for OS (p < 0.001), time to PSA progression (p = 0.043), and PSA decline (p = 0.002). Potential limitations include the retrospective study design and subjective nature of ECOG PS classification. Conclusions ECOG PS ≥2 mCRPC patients treated with abiraterone have inferior outcomes compared with ECOG 0-1 patients, especially in regard to OS. These data indicate that early initiation of abiraterone prior to a decline in PS may be warranted. Patient summary We found that advanced prostate cancer patients who have worse performance status (PS) derive less benefit from abiraterone, indicating that earlier treatment before PS declines could improve outcomes.
AB - Background Although abiraterone acetate (abiraterone) has proven efficacy in two randomised phase 3 trials in metastatic castration-resistant prostate cancer (mCRPC), patients who had an Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤2 were either excluded or under-represented in these trials. Objective To compare outcomes in ECOG PS 0-1 and ≤2 in mCRPC patients treated with abiraterone. Design, setting, and participants Cancer registries from three Canadian centres were used to retrospectively identify mCRPC patients (postdocetaxel and docetaxel-naïve) treated with abiraterone. ECOG PS, clinicopathologic characteristics, prostate-specific antigen (PSA) response, and survival data were collected. Outcome measurements and statistical analysis Survival outcomes were estimated using the Kaplan-Meier method and compared using the log-rank test. Cox proportional hazards modelling was used to examine the effect of clinicopathologic characteristics on overall survival (OS) and time to PSA progression. Results and limitations A total of 519 patients were identified; 61% (n = 318) and 39% (n = 201) were ECOG PS 0-1 and ≤2, respectively. ECOG PS 0-1 patients were significantly more likely than PS ≤2 patients to achieve a PSA decline ≤50% from baseline (45% vs 32%; p = 0.003, Fisher exact test) and had significantly longer median time to PSA progression (5.2 mo vs 4.1 mo; p = 0.023), median treatment duration (7.4 mo vs 4.5 mo; p < 0.001), and median OS (20.0 mo vs 9.1 mo; p < 0.001). On multivariate analysis, ECOG PS was a significant factor for OS (p < 0.001), time to PSA progression (p = 0.043), and PSA decline (p = 0.002). Potential limitations include the retrospective study design and subjective nature of ECOG PS classification. Conclusions ECOG PS ≥2 mCRPC patients treated with abiraterone have inferior outcomes compared with ECOG 0-1 patients, especially in regard to OS. These data indicate that early initiation of abiraterone prior to a decline in PS may be warranted. Patient summary We found that advanced prostate cancer patients who have worse performance status (PS) derive less benefit from abiraterone, indicating that earlier treatment before PS declines could improve outcomes.
KW - Abiraterone acetate
KW - Castration-resistant prostate cancer
KW - ECOG
KW - Performance status
KW - Prostate cancer
UR - http://www.scopus.com/inward/record.url?scp=84922248732&partnerID=8YFLogxK
U2 - 10.1016/j.eururo.2014.01.030
DO - 10.1016/j.eururo.2014.01.030
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C2 - 24508071
AN - SCOPUS:84922248732
VL - 67
SP - 441
EP - 447
JO - European Urology
JF - European Urology
SN - 0302-2838
IS - 3
ER -