Ceramides and response to dual secondary hormonal therapy in metastatic castration-resistant prostate cancer (mCRPC) among Black men.

5082 Background: Multiple reports suggest that Black patients with mCRPC have different responses to radiation, immunotherapy, chemotherapy, and secondary hormonal therapy compared with White patients with mCRPC. In our prospective trial of combination therapy with apalutamide (Apa) and abiraterone acetate (AA) plus prednisone (P) among Black and White men with mCRPC (PANTHER, ClinicalTrials.gov identifier NCT03098836), 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. Our previously reported exploratory genome-wide analysis identified genetic ancestry-related single nucleotide polymorphisms in genes that were known to play a role in ceramide metabolism that associated with time to prostate specific antigen (PSA) progression on AA + P therapy in mCRPC. Ceramides are associated with cancer biology and therapeutic outcomes, with ceramide Cer(d18:1/20:0), in particular, having been reported as a biomarker for colon cancer. Ceramide Synthase 4 (CerS4), which produces Cer(d18:1/20:0), has been reported to be associated with worse prognosis in colorectal cancer. We therefore hypothesized that expression of distinct ceramide species may be associated with rPFS or OS among Black and White patients with mCRPC treated with combination Apa and AA + P in the PANTHER study. Methods: Serum from 37 White and 28 Black patients enrolled in the PANTHER study who had fasted for 8-12 hours was collected and evaluable at baseline. Metabolomic profiling was done using the Biocrates MxP Quant 500 Kit. Median levels for each of 26 ceramides were calculated using the study population 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 ceramide expression. Models were stratified by race. Results: In the PANTHER study, among Black patients, expression of Cer(d18:1/20:0) was associated with rPFS (HR 4.02; 95% CI 1.06, 15.2; p value = 0.041), but there was no significant association found among White patients. Expression of Cer(d18:1/20:0) was also associated with improved OS among Black patients (HR 4.82; 95% CI 1.51, 15.4; p = 0.008), but there was no significant association found among White patients. No significant associations were found with any other ceramides. Conclusions: Our study showed that Cer(d18:1/20:0) associated with prolonged rPFS and OS among Black patients with mCRPC treated with the combination of Apa and AA + P therapy. Pending validation, this distinct ceramide species has potential to serve as a predictive indicator of response to combination Apa and AA + P therapy among Black mCRPC patients. Drug and funding for Abi Race and PANTHER provided by Janssen Scientific Affairs, LLC.

Authors

Institutions

Publication Details

Journal
Journal of Clinical Oncology
Published
2025-05-28
DOI
https://doi.org/10.1200/jco.2025.43.16_suppl.5082
Primary Topic
Sphingolipid Metabolism and Signaling
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ceramides and response to dual secondary hormonal therapy in metastatic castration-resistant prostate cancer (mCRPC) among Black men.

Donna Allen, Kellie Shobe, Sean A. Piwarski, Jennifer A. Freedman et al.
Journal of Clinical Oncology
Sphingolipid Metabolism and Signaling
article

Ceramides and response to dual secondary hormonal therapy in metastatic castration-resistant prostate cancer (mCRPC) among Black men.

Donna Allen, Kellie Shobe, Sean A. Piwarski, Jennifer A. Freedman, Marco Reyes-Martinez, Lauren E. Howard, Nicholas Bachelder, Monika Anand, Andrew J. Armstrong, Julie J.G. Kephart, Daniel J. George, Julia Hurrelbrink, Alison Clayton, Susan Halabi, Terry Hyslop, Steven R. Patierno, Bonnie LaCroix, Julia Rasmussen, Morgan Paul
article en

Abstract

5082 Background: Multiple reports suggest that Black patients with mCRPC have different responses to radiation, immunotherapy, chemotherapy, and secondary hormonal therapy compared with White patients with mCRPC. In our prospective trial of combination therapy with apalutamide (Apa) and abiraterone acetate (AA) plus prednisone (P) among Black and White men with mCRPC (PANTHER, ClinicalTrials.gov identifier NCT03098836), 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. Our previously reported exploratory genome-wide analysis identified genetic ancestry-related single nucleotide polymorphisms in genes that were known to play a role in ceramide metabolism that associated with time to prostate specific antigen (PSA) progression on AA + P therapy in mCRPC. Ceramides are associated with cancer biology and therapeutic outcomes, with ceramide Cer(d18:1/20:0), in particular, having been reported as a biomarker for colon cancer. Ceramide Synthase 4 (CerS4), which produces Cer(d18:1/20:0), has been reported to be associated with worse prognosis in colorectal cancer. We therefore hypothesized that expression of distinct ceramide species may be associated with rPFS or OS among Black and White patients with mCRPC treated with combination Apa and AA + P in the PANTHER study. Methods: Serum from 37 White and 28 Black patients enrolled in the PANTHER study who had fasted for 8-12 hours was collected and evaluable at baseline. Metabolomic profiling was done using the Biocrates MxP Quant 500 Kit. Median levels for each of 26 ceramides were calculated using the study population 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 ceramide expression. Models were stratified by race. Results: In the PANTHER study, among Black patients, expression of Cer(d18:1/20:0) was associated with rPFS (HR 4.02; 95% CI 1.06, 15.2; p value = 0.041), but there was no significant association found among White patients. Expression of Cer(d18:1/20:0) was also associated with improved OS among Black patients (HR 4.82; 95% CI 1.51, 15.4; p = 0.008), but there was no significant association found among White patients. No significant associations were found with any other ceramides. Conclusions: Our study showed that Cer(d18:1/20:0) associated with prolonged rPFS and OS among Black patients with mCRPC treated with the combination of Apa and AA + P therapy. Pending validation, this distinct ceramide species has potential to serve as a predictive indicator of response to combination Apa and AA + P therapy among Black mCRPC patients. Drug and funding for Abi Race and PANTHER provided by Janssen Scientific Affairs, LLC.

Journal of Clinical OncologyVol. 43(16_suppl)
Thomas Jefferson University (US), Sidney Kimmel Cancer Center (US)
Janssen Scientific Affairs
Openalex Percentile: Top 89%
Sphingolipid Metabolism and Signaling
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.