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Assessing sociodemographic and regional disparities in Oncotype DX Genomic Prostate Score uptake.

Authors :
Mukand NH
Chirikova E
Lichtensztajn D
Negoita S
Aboushwareb T
Bennett J
Brooks JD
Leppert JT
Chung BI
Li C
Schwartz SM
Gershman ST
Insaf T
Morawski BM
Stroup A
Wu XC
Doherty JA
Petkov VI
Zambon JP
Gomez SL
Cheng I
Source :
Cancer [Cancer] 2024 Aug 19. Date of Electronic Publication: 2024 Aug 19.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Background: The Oncotype DX Genomic Prostate Score (ODX-GPS) is a gene expression assay that predicts disease aggressiveness. The objective of this study was to identify sociodemographic and regional factors associated with ODX-GPS uptake.<br />Methods: Data from Surveillance Epidemiology and End Results registries on men with localized prostate cancer with a Gleason score of 3 + 3 or 3 + 4, PSA ≤20 ng/mL, and stage T1c to T2c disease from 2013 through 2017 were linked with ODX-GPS data. Census-tract level neighborhood socioeconomic status (nSES) quintiles were constructed using a composite socioeconomic score. Multivariable logistic regression was used to estimate the associations of ODX-GPS uptake with age at diagnosis, race and ethnicity, nSES, geographic region, insurance type, and marital status, accounting for National Comprehensive Cancer Network risk group, year of diagnosis, and clustering by census tract.<br />Results: Among 111,434 eligible men, 5.5% had ODX-GPS test uptake. Of these, 78.3% were non-Hispanic White, 9.6% were Black, 6.7% were Hispanic, and 3.6% were Asian American. Black men had the lowest odds of ODX-GPS uptake (odds ratio, 0.70; 95% confidence interval [CI], 0.63-0.76). Those in the highest versus lowest quintile of nSES were 1.64 times more likely (95% CI, 1.38-2.94) to have ODX-GPS uptake. The odds of ODX-GPS uptake were statistically significantly higher among men residing in the Northeast, West, and Midwest compared to the South.<br />Conclusions: Disparities in ODX-GPS uptake by race, ethnicity, nSES, and geographical region were identified. Concerted efforts should be made to ensure that this clinical test is equitably available.<br /> (© 2024 American Cancer Society.)

Details

Language :
English
ISSN :
1097-0142
Database :
MEDLINE
Journal :
Cancer
Publication Type :
Academic Journal
Accession number :
39158464
Full Text :
https://doi.org/10.1002/cncr.35511