Socioecologic Factors and Racial Differences in Breast Cancer Multigene Prognostic Scores in US Women

被引:0
|
作者
Parab, Ashwini Z. [2 ]
Kong, Angela [2 ]
Lee, Todd A. [2 ]
Kim, Kibum [2 ]
Nutescu, Edith A. [3 ,4 ]
Malecki, Kristen C. [5 ,6 ]
Hoskins, Kent F. [6 ,7 ]
Calip, Gregory S. [1 ,8 ]
机构
[1] Univ Southern Calif, Titus Family Dept Clin Pharm, Program Med & Publ Hlth, 1989 Zonal Ave, Los Angeles, CA 90089 USA
[2] Univ Illinois, Dept Pharm Syst Outcomes & Policy, Chicago, IL USA
[3] Univ Illinois, Dept Pharm Practice, Chicago, IL USA
[4] Univ Illinois, Ctr Pharmacoepidemiol & Pharmacoecon Res, Chicago, IL USA
[5] Univ Illinois, Sch Publ Hlth, Chicago, IL USA
[6] Univ Illinois, Canc Ctr, Chicago, IL USA
[7] Univ Illinois, Coll Med, Div Hematol & Oncol, Chicago, IL USA
[8] Univ Southern Calif, Titus Family Dept Clin Pharm, Los Angeles, CA 90089 USA
关键词
EARLY-STAGE; SOCIOECONOMIC-STATUS; HORMONE-RECEPTOR; DISPARITIES; DIAGNOSIS; SURVIVAL; NEIGHBORHOOD; MEDIATION; OUTCOMES;
D O I
10.1001/jamanetworkopen.2024.4862
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Importance Disproportionately aggressive tumor biology among non-Hispanic Black women with early-stage, estrogen receptor (ER)-positive breast cancer contributes to racial disparities in breast cancer mortality. It is unclear whether socioecologic factors underlie racial differences in breast tumor biology. Objective To examine individual-level (insurance status) and contextual (area-level socioeconomic position and rural or urban residence) factors as possible mediators of racial and ethnic differences in the prevalence of ER-positive breast tumors with aggressive biology, as indicated by a high-risk gene expression profile. Design, Setting, and Participants This retrospective cohort study included women 18 years or older diagnosed with stage I to II, ER-positive breast cancer between January 1, 2007, and December 31, 2015. All data analyses were conducted between December 2022 and April 2023. Main Outcomes and Measures The primary outcome was the likelihood of a high-risk recurrence score (RS) (>= 26) on the Oncotype DX 21-gene breast tumor prognostic genomic biomarker. Results Among 69 139 women (mean [SD] age, 57.7 [10.5] years; 6310 Hispanic [9.1%], 274 non-Hispanic American Indian and Alaskan Native [0.4%], 6017 non-Hispanic Asian and Pacific Islander [8.7%], 5380 non-Hispanic Black [7.8%], and 51 158 non-Hispanic White [74.0%]) included in our analysis, non-Hispanic Black (odds ratio [OR], 1.33; 95% CI, 1.23-1.43) and non-Hispanic American Indian and Alaska Native women (OR, 1.38; 95% CI, 1.01-1.86) had greater likelihood of a high-risk RS compared with non-Hispanic White women. There were no significant differences among other racial and ethnic groups. Compared with non-Hispanic White patients, there were greater odds of a high-risk RS for non-Hispanic Black women residing in urban areas (OR, 1.35; 95% CI, 1.24-1.46), but not among rural residents (OR, 1.05; 95% CI, 0.77-1.41). Mediation analysis demonstrated that lack of insurance, county-level disadvantage, and urban vs rural residence partially explained the greater odds of a high-risk RS among non-Hispanic Black women (proportion mediated, 17%; P < .001). Conclusions and Relevance The findings of this cohort study suggest that the consequences of structural racism extend beyond inequities in health care to drive disparities in breast cancer outcome. Additional research is needed with more comprehensive social and environmental measures to better understand the influence of social determinants on aggressive ER-positive tumor biology among racial and ethnic minoritized women from disadvantaged and historically marginalized communities.
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页数:12
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