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.

D Daniel J. George (Duke Cancer Institute, Duke University School of Medicine, Durham, NC) L Lauren Howard S 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...) T Terry Hyslop (Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA) B Bonnie LaCroix (Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC) A Alvin M. Matsumoto (University of Washington, Seattle, WA) J Julia Hurrelbrink (Duke University Health System, Durham, NC) J Julie Kephart (Duke Cancer Institute, Durham, NC) J Julia Rasmussen (Duke Cancer Institute, Durham, NC) M Marco Reyes-Martinez (Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, NC) K Kellie Shobe (Duke Cancer Institute, Durham, NC) S Steven Gray (Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC) M Monika Anand (Duke University) S Steven R. Patierno (Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, NC) A Andrew J. Armstrong R Robert Bruce Montgomery (University of Washington, Fred Hutchinson Cancer Center, Seattle, WA) E Elahe A. Mostaghel (VA Puget Sound Health Care System, Seattle, WA) J Jennifer A. Freedman (Duke University School of Medicine, Durham, NC)

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

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

D

Daniel J. George

Duke Cancer Institute, Duke University School of Medicine, Durham, NC

L

Lauren Howard

S

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...

T

Terry Hyslop

Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University, Philadelphia, PA

B

Bonnie LaCroix

Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC

A

Alvin M. Matsumoto

University of Washington, Seattle, WA

J

Julia Hurrelbrink

Duke University Health System, Durham, NC

J

Julie Kephart

Duke Cancer Institute, Durham, NC

J

Julia Rasmussen

Duke Cancer Institute, Durham, NC

M

Marco Reyes-Martinez

Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, NC

K

Kellie Shobe

Duke Cancer Institute, Durham, NC

S

Steven Gray

Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC

M

Monika Anand

Duke University

S

Steven R. Patierno

Duke Cancer Institute Center for Prostate & Urologic Cancers, Durham, NC

A

Andrew J. Armstrong

R

Robert Bruce Montgomery

University of Washington, Fred Hutchinson Cancer Center, Seattle, WA

E

Elahe A. Mostaghel

VA Puget Sound Health Care System, Seattle, WA

J

Jennifer A. Freedman

Duke University School of Medicine, Durham, NC