Abi Race: A prospective, multicenter study of black (B) and white (W) patients (pts) with metastatic castrate resistant prostate cancer (mCRPC) treated with abiraterone acetate and prednisone (AAP).

Author:

George Daniel J.1,Heath Elisabeth I.2,Sartor A. Oliver3,Sonpavde Guru4,Berry William R.5,Healy Patrick6,Winters Carolyn1,Riggan Colleen7,Anand Monika1,Kephart Julie7,Milowsky Matthew I.8,Fleming Mark T.9,Balaji K. C.10,Zhang Tian11,Bitting Rhonda L.12,Harrison Michael Roger13,McNamara Megan Ann14,Freedman Jennifer A.11,Halabi Susan11,Armstrong Andrew J.6,Bruner Deborah15

Affiliation:

1. Duke University, Durham, NC;

2. Barbara Ann Karmanos Cancer Institute, Wayne State University, Detroit, MI;

3. Tulane Medical School, New Orleans, LA;

4. Dana-Farber Cancer Institute, Boston, MA;

5. Duke University School of Medicine, Raleigh, NC;

6. Duke Cancer Institute, Duke University, Durham, NC;

7. Duke Cancer Institute, Durham, NC;

8. UNC School of Medicine, Chapel Hill, NC;

9. Virginia Oncology Associates, US Oncology Research, Norfolk, VA;

10. Wake Forest University Health Sciences, Winston Salem, NC;

11. Duke University Medical Center, Durham, NC;

12. Internal Medicine, Section on Hematology and Oncology, Winston Salem, NC;

13. Duke Cancer Institute, Duke University Medical Center, Durham, NC;

14. Duke University Medical Center, Mornsville, NC;

15. Winship Cancer Institute at Emory University, Atlanta, GA;

Abstract

LBA5009 Background: Pivotal trials of AAP for patients with mCRPC enrolled few B pts, a population with a higher mortality from prostate cancer. Retrospective data suggests B pts may have higher PSA response rates than W pts treated with AAP for mCRPC. Therefore, we prospectively investigated AAP in B vs. W pts with mCRPC. Methods: Abi Race (NCT01940276) is a prospective, multicenter, parallel group study of AP in 100 men (50 B, 50 W) with mCRPC, self-identified by race. All pts received AA 1000 mg/D and P 10 mg/D (AAP) until disease progression or unacceptable adverse events (AE). The primary objective was radiographic progression-free survival (rPFS); key secondary endpoints include PSA kinetics and safety. Exploratory analyses include SNP, metabolomics and hormonal differences by race. Results: Baseline characteristics among pts were similar. The median rPFS for B and W pts was 16.8 months (mo) in each. However, PSA PFS varied by race; median PSA PFS for B and W pts were 16.6 and 11.5 mo [Table]. B pts also had numerically higher rates of ≥30%, ≥50% and ≥90% PSA decline [Table]. AEs were similar in frequency and severity by race including hypertension (42 vs 40%); however, fatigue was higher in W pts (40 vs 26%), and hypokalemia was higher in B pts (36 vs 18%). SNP profiling revealed differences in key genes involved in androgen metabolism and transport. Conclusions: This is the first prospective multicenter study by race of secondary hormonal therapy in mCRPC. B pts may have greater and more durable PSA response to AAP than W pts. SNP patterns vary by race and will be evaluated for prognostic significance. Further prospective studies in B pts are possible and needed to understand the impact of racial determinants on outcome of new hormonal regimens. Clinical trial information: NCT01940276. [Table: see text]

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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