Race, Ethnicity, and Clinical Outcomes in Hormone Receptor-Positive, HER2-Negative, Node-Negative Breast Cancer in the Randomized TAILORx Trial
- PMID: 32986828
- PMCID: PMC8599918
- DOI: 10.1093/jnci/djaa148
Race, Ethnicity, and Clinical Outcomes in Hormone Receptor-Positive, HER2-Negative, Node-Negative Breast Cancer in the Randomized TAILORx Trial
Abstract
Background: Black race is associated with worse outcomes in early breast cancer. We evaluated clinicopathologic characteristics, the 21-gene recurrence score (RS), treatment delivered, and clinical outcomes by race and ethnicity among women who participated in the Trial Assigning Individualized Options for Treatment.
Methods: The association between clinical outcomes and race (White, Black, Asian, other or unknown) and ethnicity (Hispanic vs non-Hispanic) was examined using proportional hazards models. All P values are 2-sided.
Results: Of 9719 eligible women with hormone receptor-positive, HER2-negative, node-negative breast cancer, there were 8189 (84.3%) Whites, 693 (7.1%) Blacks, 405 (4.2%) Asians, and 432 (4.4%) with other or unknown race. Regarding ethnicity, 889 (9.1%) were Hispanic. There were no substantial differences in RS or ESR1, PGR, or HER2 RNA expression by race or ethnicity. After adjustment for other covariates, compared with White race, Black race was associated with higher distant recurrence rates (hazard ratio [HR] = 1.60, 95% confidence intervals [CI] = 1.07 to 2.41) and worse overall survival in the RS 11-25 cohort (HR = 1.51, 95% CI = 1.06 to 2.15) and entire population (HR = 1.41, 95% CI = 1.05 to 1.90). Hispanic ethnicity and Asian race were associated with better outcomes. There was no evidence of chemotherapy benefit for any racial or ethnic group in those with a RS of 11-25.
Conclusions: Black women had worse clinical outcomes despite similar 21-gene assay RS results and comparable systemic therapy in the Trial Assigning Individualized Options for Treatment. Similar to Whites, Black women did not benefit from adjuvant chemotherapy if the 21-gene RS was 11-25. Further research is required to elucidate the basis for this racial disparity in prognosis.
© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.
Figures
Comment in
-
Disparities in Breast Cancer: Narrowing the Gap.J Natl Cancer Inst. 2021 Apr 6;113(4):349-350. doi: 10.1093/jnci/djaa150. J Natl Cancer Inst. 2021. PMID: 32986842 Free PMC article. No abstract available.
-
Racial and ethnic disparities in breast cancer survival: critical appraisal of the data emerging from the randomized TAILORx.Ann Transl Med. 2022 Dec;10(23):1294. doi: 10.21037/atm-2022-64. Ann Transl Med. 2022. PMID: 36618783 Free PMC article. No abstract available.
-
Race, ethnicity, and clinical outcomes in hormone receptor-positive, human epidermal growth factor 2 negative (HER2-), node negative breast cancer in the randomized TAILORx trial: gaps in biologic and social determinants of health.Ann Transl Med. 2022 Dec;10(24):1416. doi: 10.21037/atm-2022-59. Ann Transl Med. 2022. PMID: 36660702 Free PMC article. No abstract available.
References
-
- DeSantis CE, Fedewa SA, Goding Sauer A, Kramer JL, Smith RA, Jemal A.. Breast cancer statistics, 2015: convergence of incidence rates between black and white women. CA Cancer J Clin. 2016;66(1):31–42. - PubMed
-
- Bach PB, Schrag D, Brawley OW, Galaznik A, Yakren S, Begg CB.. Survival of blacks and whites after a cancer diagnosis. JAMA. 2002;287(16):2106–2113. - PubMed
-
- Crew KD, Neugut AI, Wang X, et al. Racial disparities in treatment and survival of male breast cancer. J Clin Oncol. 2007;25(9):1089–1098. - PubMed
-
- Newman LA, Mason J, Cote D, et al. African-American ethnicity, socioeconomic status, and breast cancer survival: a meta-analysis of 14 studies involving over 10,000 African-American and 40,000 White American patients with carcinoma of the breast. Cancer. 2002;94(11):2844–2854. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- U10 CA180868/CA/NCI NIH HHS/United States
- UG1 CA190140/CA/NCI NIH HHS/United States
- U24 CA196172/CA/NCI NIH HHS/United States
- U10 CA180821/CA/NCI NIH HHS/United States
- P50 CA098131/CA/NCI NIH HHS/United States
- U10 CA180863/CA/NCI NIH HHS/United States
- U10 CA180820/CA/NCI NIH HHS/United States
- UG1 CA233253/CA/NCI NIH HHS/United States
- U10 CA180822/CA/NCI NIH HHS/United States
- UG1 CA189804/CA/NCI NIH HHS/United States
- UG1 CA233270/CA/NCI NIH HHS/United States
- UG1 CA189867/CA/NCI NIH HHS/United States
- UG1 CA189859/CA/NCI NIH HHS/United States
- UG1 CA189869/CA/NCI NIH HHS/United States
- UG1 CA189974/CA/NCI NIH HHS/United States
- UG1 CA233160/CA/NCI NIH HHS/United States
- UG1 CA232760/CA/NCI NIH HHS/United States
- UG1 CA189828/CA/NCI NIH HHS/United States
- UG1 CA233373/CA/NCI NIH HHS/United States
- UG1 CA233247/CA/NCI NIH HHS/United States
- U10 CA180794/CA/NCI NIH HHS/United States
- U10 CA180888/CA/NCI NIH HHS/United States
- UG1 CA233184/CA/NCI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous
