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Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer

To evaluate the racial and ethnic differences in prevalence of germline pathogenic variants (PVs) and the effect of race and ethnicity on breast cancer (BC) risk among carriers, results of multigene testing of 77 900 women with BC (non-Hispanic White [NHW] = 57 003; Ashkenazi-Jewish = 4798; Black =...

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Autores principales: Yadav, Siddhartha, LaDuca, Holly, Polley, Eric C, Hu, Chunling, Niguidula, Nancy, Shimelis, Hermela, Lilyquist, Jenna, Na, Jie, Lee, Kun Y, Gutierrez, Stephanie, Yussuf, Amal, Hart, Steven N, Davis, Brigette Tippin, Chao, Elizabeth C, Pesaran, Tina, Goldgar, David E, Dolinsky, Jill S, Couch, Fergus J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633452/
https://www.ncbi.nlm.nih.gov/pubmed/33146377
http://dx.doi.org/10.1093/jnci/djaa167
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author Yadav, Siddhartha
LaDuca, Holly
Polley, Eric C
Hu, Chunling
Niguidula, Nancy
Shimelis, Hermela
Lilyquist, Jenna
Na, Jie
Lee, Kun Y
Gutierrez, Stephanie
Yussuf, Amal
Hart, Steven N
Davis, Brigette Tippin
Chao, Elizabeth C
Pesaran, Tina
Goldgar, David E
Dolinsky, Jill S
Couch, Fergus J
author_facet Yadav, Siddhartha
LaDuca, Holly
Polley, Eric C
Hu, Chunling
Niguidula, Nancy
Shimelis, Hermela
Lilyquist, Jenna
Na, Jie
Lee, Kun Y
Gutierrez, Stephanie
Yussuf, Amal
Hart, Steven N
Davis, Brigette Tippin
Chao, Elizabeth C
Pesaran, Tina
Goldgar, David E
Dolinsky, Jill S
Couch, Fergus J
author_sort Yadav, Siddhartha
collection PubMed
description To evaluate the racial and ethnic differences in prevalence of germline pathogenic variants (PVs) and the effect of race and ethnicity on breast cancer (BC) risk among carriers, results of multigene testing of 77 900 women with BC (non-Hispanic White [NHW] = 57 003; Ashkenazi-Jewish = 4798; Black = 6722; Hispanic = 5194; and Asian = 4183) were analyzed, and the frequency of PVs in each gene were compared between BC patients (cases) and race- and ethnicity-matched gnomAD reference controls. Compared with NHWs, BRCA1 PVs were enriched in Ashkenazi-Jews and Hispanics, whereas CHEK2 PVs were statistically significantly lower in Blacks, Hispanics, and Asians (all 2-sided P < .05). In case-control studies, BARD1 PVs were associated with high risks (odds ratio > 4.00) of BC in Blacks, Hispanics, and Asians; ATM PVs were associated with increased risk of BC among all races and ethnicities except Asians, whereas CHEK2 and BRIP1 PVs were associated with increased risk of BC among NHWs and Hispanics only. These findings suggest a need for personalized management of BC risk in PV carriers based on race and ethnicity.
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spelling pubmed-86334522021-12-01 Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer Yadav, Siddhartha LaDuca, Holly Polley, Eric C Hu, Chunling Niguidula, Nancy Shimelis, Hermela Lilyquist, Jenna Na, Jie Lee, Kun Y Gutierrez, Stephanie Yussuf, Amal Hart, Steven N Davis, Brigette Tippin Chao, Elizabeth C Pesaran, Tina Goldgar, David E Dolinsky, Jill S Couch, Fergus J J Natl Cancer Inst Brief Communication To evaluate the racial and ethnic differences in prevalence of germline pathogenic variants (PVs) and the effect of race and ethnicity on breast cancer (BC) risk among carriers, results of multigene testing of 77 900 women with BC (non-Hispanic White [NHW] = 57 003; Ashkenazi-Jewish = 4798; Black = 6722; Hispanic = 5194; and Asian = 4183) were analyzed, and the frequency of PVs in each gene were compared between BC patients (cases) and race- and ethnicity-matched gnomAD reference controls. Compared with NHWs, BRCA1 PVs were enriched in Ashkenazi-Jews and Hispanics, whereas CHEK2 PVs were statistically significantly lower in Blacks, Hispanics, and Asians (all 2-sided P < .05). In case-control studies, BARD1 PVs were associated with high risks (odds ratio > 4.00) of BC in Blacks, Hispanics, and Asians; ATM PVs were associated with increased risk of BC among all races and ethnicities except Asians, whereas CHEK2 and BRIP1 PVs were associated with increased risk of BC among NHWs and Hispanics only. These findings suggest a need for personalized management of BC risk in PV carriers based on race and ethnicity. Oxford University Press 2020-11-04 /pmc/articles/PMC8633452/ /pubmed/33146377 http://dx.doi.org/10.1093/jnci/djaa167 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Brief Communication
Yadav, Siddhartha
LaDuca, Holly
Polley, Eric C
Hu, Chunling
Niguidula, Nancy
Shimelis, Hermela
Lilyquist, Jenna
Na, Jie
Lee, Kun Y
Gutierrez, Stephanie
Yussuf, Amal
Hart, Steven N
Davis, Brigette Tippin
Chao, Elizabeth C
Pesaran, Tina
Goldgar, David E
Dolinsky, Jill S
Couch, Fergus J
Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
title Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
title_full Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
title_fullStr Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
title_full_unstemmed Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
title_short Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer
title_sort racial and ethnic differences in multigene hereditary cancer panel test results for women with breast cancer
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633452/
https://www.ncbi.nlm.nih.gov/pubmed/33146377
http://dx.doi.org/10.1093/jnci/djaa167
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