Predictive associations between serum dehydroepiandrosterone sulfate (DHEAS) and race among patients (pts) treated with apalutamide (apa), abiraterone acetate (AA) plus prednisone (P) in the PANTHER study.
Abstract
e17076 Background: PANTHER is a multicenter prospective trial of Black and White cohorts of metastatic castration resistant prostate cancer (mCRPC) patients (pts) treated with open label Apa and AA +P. We previously reported the 24-month radiographic progression-free survival (rPFS) for Black and White men were 61% (95% CI 49, 78) and 38% (95% CI 27, 54), while the 36-month overall survival (OS) rates were 68% (95% CI 55, 83) and 50% (95% CI 37, 66), respectively. In contrast, a similarly designed prospective study in mCRPC pts treated with AA + P (Abi Race) demonstrated no clear differences in rPFS or OS. We explored baseline hormonal levels associated with race in PANTHER and Abi Race, and their association with treatment outcomes. Methods: We measured levels of 12 steroid hormones using LC/MS-MS in available serum samples obtained at baseline and at 4 weeks of therapy from 161 of the 193 patients enrolled in PANTHER (n=86) and in Abi Race (n=75). Samples were batched and all sera assessed contemporaneously. Median levels for each hormone were calculated combining both study populations and used as a cut point. Cox proportional hazard models were used to calculate the hazard ratio for rPFS and OS associated with above or below median in the overall populations and stratified by race. Results: Median baseline DHEAS was 49 mg/dl, with Black pts demonstrating a slightly higher median level (52 mg/dl; range 7-248) than White pts (42 mg/dl; 4-220). BaselineDHEAS levels below the median demonstrated a non-significant trend towards shorter outcomes in Abi Race: rPFS (HR 1.22, 95% CI 0.70, 2.15) and OS (HR 1.20; 95% CI 0.66, 2.18), and in PANTHER: rPFS (HR 1.54, 95% 0.87, 2.73) and OS (HR 1.14; 95% CI 0.67,1.95). When evaluated by race and DHEAS levels, patients in Abi Race demonstrated no clear association with outcomes. In contrast, Black patients with elevated DHEAS levels in PANTHER demonstrated the greatest rPFS and OS, with significant differences in HRs compared to White patients, ranging from 2.65 to 3.67 for rPFS and 2.20 to 2.43 for OS (see Table). Conclusions: Elevated baseline DHEAS levels may have positive predictive significance for rPFS and OS in Black men treated with combination Apa and AA + P compared to White men, but not when treated with AA + P alone. Larger prospective studies are needed. If confirmed, these results support the hypothesis that some Black men may disproportionately benefit from combined androgen signaling pathway inhibition. Clinical trial information: NCT03098836 . Baseline DHEAS levels, race, and treatment outcome in Abi Race and PANTHER. Abi Race PANTHER rPFS Race DHEAS n HR 95% CI p-value n HR 95% CI p-value Black pts >Median 20 -- -- 0.80 24 -- -- 0.018 Black pts ≤Median 21 1.53 0.71, 3.28 19 1.81 0.67, 4.85 White pts >Median 16 1.25 0.55, 2.84 25 2.65 1.08, 6.50 White pts ≤Median 22 1.18 0.52, 2.67 24 3.67 1.51, 8.95 OS Black pts >Median 20 -- -- 0.50 24 -- -- 0.086 Black pts ≤Median 21 1.62 0.72, 3.65 19 1.46 0.61, 3.51 White pts >Median 16 1.01 0.41, 2.50 25 2.43 1.12, 5.27 White pts ≤Median 22 0.91 0.38, 2.13 24 2.20 1.00, 4.86
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (18)
Daniel J. George
Duke Cancer Institute, Duke University School of Medicine, Durham, NC
Lauren Howard
Susan Halabi
From the Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda (A.B.A., N.S., S.N., L.L., L.C.), the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore (J.H.-C.), and the Investigational Drug Branch, Cancer Therapy Evaluation Program, National Cancer Institute, National Institutes of Health, Rockville (H.S., E.S.) — all in Maryland; the Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN (K.V.B., M.O., C.M., G.P.B.); AdventHealth Cancer Institute and the University of Central Florida, Orlando (G.S.); Dana–Farber/Harvard Cancer Center, Boston (S.B., B.M.); UNC Lineberger Comprehensive Cancer Center, Chapel Hill (W.Y.K.), and Duke University Medical Center and Duke Cancer Institute, Durham (J.H., S.H.) — both in North Carolina; the University of Kansas Cancer Center, Westwood (R.P.); Memorial Sloan Kettering Cancer Center, New York (M.Y.T., M.J.M., J.E.R.), and Roswell Park Comprehensive Cancer Center, Buffalo (G.C.) — both in...
Terry Hyslop
Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA
Bonnie LaCroix
Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC
Alvin M. Matsumoto
University of Washington, Seattle, WA
Julia Hurrelbrink
Duke University Health System, Durham, NC
Julie Kephart
Duke Cancer Institute, Durham, NC
Julia Rasmussen
Duke Cancer Institute, Durham, NC
Marco Reyes-Martinez
Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, NC
Kellie Shobe
Duke Cancer Institute, Durham, NC
Steven Gray
Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC
Monika Anand
Duke University
Steven R. Patierno
Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, NC
Andrew J. Armstrong
Robert Bruce Montgomery
University of Washington, Fred Hutchinson Cancer Center, Seattle, WA
Elahe A. Mostaghel
VA Puget Sound Health Care System, Seattle, WA
Jennifer A. Freedman
Duke University School of Medicine, Durham, NC