Racial disparities in survival outcomes among breast cancer patients by molecular subtypes.
Racial disparities in survival outcomes among breast cancer patients by molecular subtypes.
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DOI:
10.1007/s10549-020-05984-w
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发表时间:
2021-03
影响因子:
3.8
通讯作者:
Huo D
中科院分区:
文献类型:
--
作者:
Zhao F;Copley B;Niu Q;Liu F;Johnson JA;Sutton T;Khramtsova G;Sveen E;Yoshimatsu TF;Zheng Y;Ibraheem A;Jaskowiak N;Nanda R;Fleming GF;Olopade OI;Huo D
Differences in tumor biology, genomic architecture, and health care delivery patterns contribute to the breast cancer mortality gap between White and Black patients in the US. Although this gap has been well documented in previous literature, it remains uncertain how large the actual effect size of race is for different survival outcomes and the four breast cancer subtypes. We established a breast cancer patient cohort at the University of Chicago Comprehensive Cancer Center. We chose five major survival outcomes to study: overall survival, recurrence-free survival, breast-cancer-specific survival, time-to-recurrence and post-recurrence survival. Cox proportional hazards models were used to estimate the hazard ratios between Black and White patients, adjusting for selected patient, tumor and treatment characteristics, and also stratified by the four breast cancer subtypes. The study included 2795 stage I-III breast cancer patients (54% White and 38% Black). After adjusting for selected patient, tumor and treatment characteristics, Black patients still did worse than White patients in all five survival outcomes. The racial difference was highest within the HR−/HER2+ subgroup, in both overall survival (hazard ratio = 4.00, 95% CI: 1.47–10.86) and recurrence-free survival (hazard ratio = 3.00, 95% CI: 1.36–6.60), adjusting for age at diagnosis, cancer stage and comorbidities. There was also a significant racial disparity within the HR+/HER2− group in both overall survival and recurrence-free survival. Our study confirmed that racial disparity existed between White and Black breast cancer patients in terms of both survival and recurrence, and found that this disparity was largest among HR−/HER2+ and HR+/HER2− patients.
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DOI:
10.1158/1078-0432.ccr-10-1533
发表时间:
2010-12-15
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
O'Brien KM;Cole SR;Tse CK;Perou CM;Carey LA;Foulkes WD;Dressler LG;Geradts J;Millikan RC
通讯作者:
Millikan RC
DOI:
10.1158/1055-9965.epi-15-0243
发表时间:
2015-07
期刊:
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
影响因子:
--
作者:
Tao L;Gomez SL;Keegan TH;Kurian AW;Clarke CA
通讯作者:
Clarke CA
影响因子:
7.2
作者:
DEYO, RA;CHERKIN, DC;CIOL, MA
通讯作者:
CIOL, MA
DOI:
10.6004/jnccn.2014.0058
发表时间:
2014-04-01
影响因子:
13.4
作者:
Gradishar, William J.;Anderson, Benjamin O.;Kumar, Rashmi
通讯作者:
Kumar, Rashmi
影响因子:
45.3
作者:
Partridge, AH;Wang, PS;Avorn, J
通讯作者:
Avorn, J