4.7 Article

A prospective trial of abiraterone acetate plus prednisone in Black and White men with metastatic castrate-resistant prostate cancer

期刊

CANCER
卷 127, 期 16, 页码 2954-2965

出版社

WILEY
DOI: 10.1002/cncr.33589

关键词

abiraterone acetate; African American; castration resistant; hormone therapy; metastatic prostate cancer; prednisone; prostate‐ specific antigen (PSA); race

类别

资金

  1. Janssen Scientific Affairs, LLC
  2. Department of Defense Congressionally Directed Medical Research Program Prostate Cancer Clinical Trials Consortium [W81XWH-09-1-0152, W81XWH-14-2-0198]
  3. National Institutes of Health/National Cancer Institute Feasibility Studies to Build Collaborative Partnerships in Cancer Research (P20) Award [1P20-CA202925-01A1]
  4. Prostate Cancer Foundation Movember Challenge Award

向作者/读者索取更多资源

Retrospective studies show that Black men with mCRPC may have longer survival compared to White men. This prospective study found that Black and White patients had similar rPFS and OS, but Black patients showed higher rates of PSA decline. Black men may experience higher rates of side effects compared to White men, indicating a need for further investigation.
Background Retrospective analyses of randomized trials suggest that Black men with metastatic castration-resistant prostate cancer (mCRPC) have longer survival than White men. The authors conducted a prospective study of abiraterone acetate plus prednisone to explore outcomes by race. Methods This race-stratified, multicenter study estimated radiographic progression-free survival (rPFS) in Black and White men with mCRPC. Secondary end points included prostate-specific antigen (PSA) kinetics, overall survival (OS), and safety. Exploratory analysis included genome-wide genotyping to identify single nucleotide polymorphisms associated with progression in a model incorporating genetic ancestry. One hundred patients self-identified as White (n = 50) or Black (n = 50) were enrolled. Eligibility criteria were modified to facilitate the enrollment of individual Black patients. Results The median rPFS for Black and White patients was 16.6 and 16.8 months, respectively; their times to PSA progression (TTP) were 16.6 and 11.5 months, respectively; and their OS was 35.9 and 35.7 months, respectively. Estimated rates of PSA decline by >= 50% in Black and White patients were 74% and 66%, respectively; and PSA declines to <0.2 ng/mL were 26% and 10%, respectively. Rates of grade 3 and 4 hypertension, hypokalemia, and hyperglycemia were higher in Black men. Conclusions Multicenter prospective studies by race are feasible in men with mCRPC but require less restrictive eligibility. Despite higher comorbidity rates, Black patients demonstrated rPFS and OS similar to those of White patients and trended toward greater TTP and PSA declines, consistent with retrospective reports. Importantly, Black men may have higher side-effect rates than White men. This exploratory genome-wide analysis of TTP identified a possible candidate marker of ancestry-dependent treatment outcomes.

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