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Am J Prev Med. 2021 Feb;60(2):e85-e94. doi: 10.1016/j.amepre.2020.08.029. Epub 2020 Nov 7.
2
Predictors of BRCA1/2 genetic testing among Black women with breast cancer: a population-based study.黑人乳腺癌女性中BRCA1/2基因检测的预测因素:一项基于人群的研究。
Cancer Med. 2017 Jul;6(7):1787-1798. doi: 10.1002/cam4.1120. Epub 2017 Jun 19.
3
Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.基于人群的年轻乳腺癌幸存者样本中BRCA检测与癌症风险管理的种族差异。
Cancer. 2017 Jul 1;123(13):2497-2505. doi: 10.1002/cncr.30621. Epub 2017 Feb 9.
4
Effective Referral of Low-Income Women at Risk for Hereditary Breast and Ovarian Cancer to Genetic Counseling: A Randomized Delayed Intervention Control Trial.将有遗传性乳腺癌和卵巢癌风险的低收入女性有效转诊至遗传咨询:一项随机延迟干预对照试验。
Am J Public Health. 2016 Oct;106(10):1842-8. doi: 10.2105/AJPH.2016.303312. Epub 2016 Aug 23.
5
Health Care Segregation, Physician Recommendation, and Racial Disparities in BRCA1/2 Testing Among Women With Breast Cancer.医疗保健隔离、医生建议与乳腺癌女性BRCA1/2检测中的种族差异
J Clin Oncol. 2016 Aug 1;34(22):2610-8. doi: 10.1200/JCO.2015.66.0019. Epub 2016 May 9.
6
Implementing a screening tool for identifying patients at risk for hereditary breast and ovarian cancer: a statewide initiative.实施一种用于识别遗传性乳腺癌和卵巢癌高危患者的筛查工具:一项全州范围的倡议。
Ann Surg Oncol. 2014 Oct;21(10):3342-7. doi: 10.1245/s10434-014-3921-1. Epub 2014 Jul 22.
7
African ancestry and higher prevalence of triple-negative breast cancer: findings from an international study.非洲裔血统与三阴性乳腺癌更高的患病率:来自一项国际研究的结果。
Cancer. 2010 Nov 1;116(21):4926-32. doi: 10.1002/cncr.25276.
8
Further development and evaluation of a breast/ovarian cancer genetics referral screening tool.乳腺癌/卵巢癌遗传学转诊筛查工具的进一步开发与评估
Genet Med. 2010 Apr;12(4):240. doi: 10.1097/GIM.0b013e3181d4bc3a.

筛查遗传性乳腺癌和卵巢癌风险个体:佐治亚州 2012-2020 年的全州倡议。

Screening for Individuals at Risk for Hereditary Breast and Ovarian Cancer: A Statewide Initiative, Georgia, 2012-2020.

机构信息

Julia K. Veitinger is with the Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA. Alice S. Kerber, Sheryl G. A. Gabram-Mendola, Lynn M. Durham, and Cindy Snyder are with the Georgia Center for Oncology Research and Education, Atlanta. Yuan Liu is with the Department of Biostatistics and Bioinformatics, Rollins School of Public Health & Winship Cancer Institute, Emory University. Diane Durrence, Alissa K. Berzen, and Janet Y. Shin are with the Georgia Department of Public Health, Atlanta. Cecelia A. Bellcross is with the Department of Human Genetics, Emory University School of Medicine, Atlanta. Yue Guan is with Department of Behavioral, Social, and Health Education Sciences, Rollins School of Public Health, Emory University.

出版信息

Am J Public Health. 2022 Sep;112(9):1249-1252. doi: 10.2105/AJPH.2022.306932. Epub 2022 Jul 21.

DOI:10.2105/AJPH.2022.306932
PMID:35862880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9382180/
Abstract

Georgia implemented a statewide family history screening program for hereditary breast and ovarian cancer. From November 2012 through December 2020, 29 090 individuals were screened, 16 679 of whom (57.3%) self-identified as a racial/ethnic minority. Of the 4% (1172/29 090) of individuals who screened as high risk, more than half underwent genetic consultation (793/1172; 67.7%) and testing (416/589; 70.6%). Compared with White women, Black and Hispanic women had higher uptake rates of genetic consultation. Public health settings serving racial minorities are well suited to address disparities in genetic service access. (. 2022;112(9):1249-1252. https://doi.org/10.2105/AJPH.2022.306932).

摘要

佐治亚州实施了一项全州范围内的遗传性乳腺癌和卵巢癌家族史筛查计划。从 2012 年 11 月至 2020 年 12 月,共有 29090 人接受了筛查,其中 16679 人(57.3%)自我认定为少数族裔。在筛查为高风险的 4%(1172/29090)的人群中,超过一半接受了遗传咨询(793/1172;67.7%)和检测(416/589;70.6%)。与白人女性相比,黑人和西班牙裔女性接受遗传咨询的比例更高。为少数族裔服务的公共卫生机构非常适合解决遗传服务获取方面的差异。(2022 年;112(9):1249-1252。https://doi.org/10.2105/AJPH.2022.306932)。