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Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ

BACKGROUND: General populations of black women have a higher risk of developing breast cancer negative for both estrogen receptor (ER) and progesterone receptor (PR) in comparison with white counterparts. Racial differences remain unknown in the risk of developing aggressive invasive breast cancer (...

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Autores principales: Liu, Ying, West, Robert, Weber, Jason D., Colditz, Graham A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717007/
https://www.ncbi.nlm.nih.gov/pubmed/31120565
http://dx.doi.org/10.1002/cncr.32200
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author Liu, Ying
West, Robert
Weber, Jason D.
Colditz, Graham A.
author_facet Liu, Ying
West, Robert
Weber, Jason D.
Colditz, Graham A.
author_sort Liu, Ying
collection PubMed
description BACKGROUND: General populations of black women have a higher risk of developing breast cancer negative for both estrogen receptor (ER) and progesterone receptor (PR) in comparison with white counterparts. Racial differences remain unknown in the risk of developing aggressive invasive breast cancer (IBC) that is characterized by negativity for both ER and PR (ER–PR–) or higher 21‐gene recurrence scores after ductal carcinoma in situ (DCIS). METHODS: This study identified 163,892 women (10.5% black, 9.8% Asian, and 8.6% Hispanic) with incident DCIS between 1990 and 2015 from the Surveillance, Epidemiology, and End Results data sets. Cox proportional hazards regression was used to estimate hazards ratios (HRs) of subsequent IBC classified by the hormone receptor status and 21‐gene recurrence scores. RESULTS: During a median follow‐up of 90 months, 8333 women developed IBC. In comparison with white women, the adjusted HR of subsequent ER–PR– breast cancer was 1.86 (95% confidence interval [CI], 1.57‐2.20) for black women (absolute 10‐year difference, 2.2%) and 1.40 (95% CI, 1.14‐1.71) for Asian women (absolute 10‐year difference, 0.4%); this was stronger than the associations for ER+ and/or PR+ subtypes (P (heterogeneity) = .0004). The 21‐gene recurrence scores of subsequent early‐stage, ER+ IBCs varied by race/ethnicity (P (heterogeneity) = .057); black women were more likely than white women to have a recurrence score of 26 or higher (HR, 1.38; 95% CI, 1.00‐1.92). No significant difference was observed in the risks of subsequent IBC subtypes for Hispanic women. CONCLUSIONS: Black and Asian women with DCIS had higher risks of developing biologically aggressive IBC than white counterparts. This should be considered in treatment decisions for black and Asian patients with DCIS.
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spelling pubmed-67170072019-10-07 Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ Liu, Ying West, Robert Weber, Jason D. Colditz, Graham A. Cancer Original Articles BACKGROUND: General populations of black women have a higher risk of developing breast cancer negative for both estrogen receptor (ER) and progesterone receptor (PR) in comparison with white counterparts. Racial differences remain unknown in the risk of developing aggressive invasive breast cancer (IBC) that is characterized by negativity for both ER and PR (ER–PR–) or higher 21‐gene recurrence scores after ductal carcinoma in situ (DCIS). METHODS: This study identified 163,892 women (10.5% black, 9.8% Asian, and 8.6% Hispanic) with incident DCIS between 1990 and 2015 from the Surveillance, Epidemiology, and End Results data sets. Cox proportional hazards regression was used to estimate hazards ratios (HRs) of subsequent IBC classified by the hormone receptor status and 21‐gene recurrence scores. RESULTS: During a median follow‐up of 90 months, 8333 women developed IBC. In comparison with white women, the adjusted HR of subsequent ER–PR– breast cancer was 1.86 (95% confidence interval [CI], 1.57‐2.20) for black women (absolute 10‐year difference, 2.2%) and 1.40 (95% CI, 1.14‐1.71) for Asian women (absolute 10‐year difference, 0.4%); this was stronger than the associations for ER+ and/or PR+ subtypes (P (heterogeneity) = .0004). The 21‐gene recurrence scores of subsequent early‐stage, ER+ IBCs varied by race/ethnicity (P (heterogeneity) = .057); black women were more likely than white women to have a recurrence score of 26 or higher (HR, 1.38; 95% CI, 1.00‐1.92). No significant difference was observed in the risks of subsequent IBC subtypes for Hispanic women. CONCLUSIONS: Black and Asian women with DCIS had higher risks of developing biologically aggressive IBC than white counterparts. This should be considered in treatment decisions for black and Asian patients with DCIS. John Wiley and Sons Inc. 2019-05-23 2019-09-15 /pmc/articles/PMC6717007/ /pubmed/31120565 http://dx.doi.org/10.1002/cncr.32200 Text en © 2019 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Liu, Ying
West, Robert
Weber, Jason D.
Colditz, Graham A.
Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
title Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
title_full Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
title_fullStr Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
title_full_unstemmed Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
title_short Race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
title_sort race and risk of subsequent aggressive breast cancer following ductal carcinoma in situ
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717007/
https://www.ncbi.nlm.nih.gov/pubmed/31120565
http://dx.doi.org/10.1002/cncr.32200
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