美国女性乳腺癌的致病变异、家族史和累积风险

IF 20.1 1区 医学 Q1 ONCOLOGY
Katie M. O’Brien, Alexander P. Keil, Jack A. Taylor, Clarice R. Weinberg, Eric C. Polley, Siddhartha Yadav, Nicholas J. Boddicker, Chunling Hu, Christine B. Ambrosone, Hoda Anton-Culver, Paul L. Auer, Clara Bodelon, Kristen Brantley, Elizabeth S. Burnside, Fei Chen, Susan M. Domchek, A. Heather Eliassen, Christopher A. Haiman, James M. Hodge, Peter Kraft, James V. Lacey, Sara Lindstroem, Maria Elena Martinez, Katherine L. Nathanson, Susan L. Neuhausen, Janet E. Olson, Julie R. Palmer, Alpa V. Patel, Kathryn L. Penney, Kathryn J. Ruddy, Christopher G. Scott, Lauren R. Teras, Amy Trentham-Dietz, Celine M. Vachon, Jeffrey N. Weitzel, Song Yao, Gary Zirpoli, Fergus J. Couch, Dale P. Sandler
{"title":"美国女性乳腺癌的致病变异、家族史和累积风险","authors":"Katie M. O’Brien, Alexander P. Keil, Jack A. Taylor, Clarice R. Weinberg, Eric C. Polley, Siddhartha Yadav, Nicholas J. Boddicker, Chunling Hu, Christine B. Ambrosone, Hoda Anton-Culver, Paul L. Auer, Clara Bodelon, Kristen Brantley, Elizabeth S. Burnside, Fei Chen, Susan M. Domchek, A. Heather Eliassen, Christopher A. Haiman, James M. Hodge, Peter Kraft, James V. Lacey, Sara Lindstroem, Maria Elena Martinez, Katherine L. Nathanson, Susan L. Neuhausen, Janet E. Olson, Julie R. Palmer, Alpa V. Patel, Kathryn L. Penney, Kathryn J. Ruddy, Christopher G. Scott, Lauren R. Teras, Amy Trentham-Dietz, Celine M. Vachon, Jeffrey N. Weitzel, Song Yao, Gary Zirpoli, Fergus J. Couch, Dale P. Sandler","doi":"10.1001/jamaoncol.2025.3875","DOIUrl":null,"url":null,"abstract":"ImportanceInherited pathogenic variants (PVs) in known predisposition genes can greatly increase breast cancer risk, but the combined impact of PV status, family history, and other factors on breast cancer risk in the general US population has not been well described.ObjectiveTo evaluate population-based breast cancer risk estimates for those with established PVs overall and stratified by first-degree family history of breast cancer and other factors.Design, Setting, and ParticipantsThis study used pooled data from 13 US-based breast cancer case-control studies participating in the Cancer Risk Estimates Related to Susceptibility (CARRIERS) consortium. Enrollment for individual studies occurred between 1976 and 2013, and results are based on data released March 2023, with analyses conducted from June 2022 to July 2025.ExposuresPVs, breast cancer family history, self-reported race and ethnicity, and established risk factors.Main Outcomes and MeasuresBreast cancer rate ratios for PVs in 7 genes were estimated from the CARRIERS consortium. PV status and incidence and mortality statistics were combined using the Individualized Coherent Absolute Risk Estimation (iCARE) model to estimate conditional cumulative breast cancer risks and 95% CIs, stratified by family history and standardized to the US population. Models that incorporated population-based data and published estimates for established epidemiologic risk factors were also evaluated.ResultsA total of 67 692 women were studied, including 33 841 who were diagnosed with breast cancer. PVs in <jats:italic>ATM</jats:italic>, <jats:italic>BRCA1</jats:italic>, <jats:italic>BRCA2</jats:italic>, <jats:italic>CHEK2</jats:italic>, and <jats:italic>PALB2</jats:italic> were strongly associated with breast cancer risk, with <jats:italic>BRCA1</jats:italic> and <jats:italic>PALB2</jats:italic> PVs showing evidence of heterogeneity by family history. In models considering PVs, family history, and established risk factors, the estimated cumulative risks of breast cancer by age 50 years ranged from 2.4% (95% CI, 2.4-2.4) in women with no PVs and no family history to 35.5% (95% CI, 21.6-55.1) in <jats:italic>PALB2</jats:italic> PV carriers with a family history. Among women who have not been diagnosed with breast cancer by age 50 years, the cumulative risk of breast cancer by age 80 years ranged from 11.1% (95% CI, 11.0-11.2) in noncarriers with no family history to 70.5% (95% CI, 52.8-83.5) for <jats:italic>PALB2</jats:italic> carriers with a family history. PV-specific cumulative risk estimates varied across subgroups defined by race and ethnicity and potentially modifiable epidemiologic risk factors.Conclusions and RelevanceIn this study, population-based estimates of cumulative breast cancer risk for established PVs, as informed by the CARRIERS case-control sample, varied by family history and potentially modifiable risk factors. These estimates provide guidance for identifying individuals who will most benefit from enhanced screening and prevention strategies.","PeriodicalId":14850,"journal":{"name":"JAMA Oncology","volume":"15 1","pages":""},"PeriodicalIF":20.1000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pathogenic Variants, Family History, and Cumulative Risk of Breast Cancer in US Women\",\"authors\":\"Katie M. O’Brien, Alexander P. Keil, Jack A. Taylor, Clarice R. Weinberg, Eric C. Polley, Siddhartha Yadav, Nicholas J. Boddicker, Chunling Hu, Christine B. Ambrosone, Hoda Anton-Culver, Paul L. Auer, Clara Bodelon, Kristen Brantley, Elizabeth S. Burnside, Fei Chen, Susan M. Domchek, A. Heather Eliassen, Christopher A. Haiman, James M. Hodge, Peter Kraft, James V. Lacey, Sara Lindstroem, Maria Elena Martinez, Katherine L. Nathanson, Susan L. Neuhausen, Janet E. Olson, Julie R. Palmer, Alpa V. Patel, Kathryn L. Penney, Kathryn J. Ruddy, Christopher G. Scott, Lauren R. Teras, Amy Trentham-Dietz, Celine M. Vachon, Jeffrey N. Weitzel, Song Yao, Gary Zirpoli, Fergus J. Couch, Dale P. Sandler\",\"doi\":\"10.1001/jamaoncol.2025.3875\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ImportanceInherited pathogenic variants (PVs) in known predisposition genes can greatly increase breast cancer risk, but the combined impact of PV status, family history, and other factors on breast cancer risk in the general US population has not been well described.ObjectiveTo evaluate population-based breast cancer risk estimates for those with established PVs overall and stratified by first-degree family history of breast cancer and other factors.Design, Setting, and ParticipantsThis study used pooled data from 13 US-based breast cancer case-control studies participating in the Cancer Risk Estimates Related to Susceptibility (CARRIERS) consortium. Enrollment for individual studies occurred between 1976 and 2013, and results are based on data released March 2023, with analyses conducted from June 2022 to July 2025.ExposuresPVs, breast cancer family history, self-reported race and ethnicity, and established risk factors.Main Outcomes and MeasuresBreast cancer rate ratios for PVs in 7 genes were estimated from the CARRIERS consortium. PV status and incidence and mortality statistics were combined using the Individualized Coherent Absolute Risk Estimation (iCARE) model to estimate conditional cumulative breast cancer risks and 95% CIs, stratified by family history and standardized to the US population. Models that incorporated population-based data and published estimates for established epidemiologic risk factors were also evaluated.ResultsA total of 67 692 women were studied, including 33 841 who were diagnosed with breast cancer. PVs in <jats:italic>ATM</jats:italic>, <jats:italic>BRCA1</jats:italic>, <jats:italic>BRCA2</jats:italic>, <jats:italic>CHEK2</jats:italic>, and <jats:italic>PALB2</jats:italic> were strongly associated with breast cancer risk, with <jats:italic>BRCA1</jats:italic> and <jats:italic>PALB2</jats:italic> PVs showing evidence of heterogeneity by family history. In models considering PVs, family history, and established risk factors, the estimated cumulative risks of breast cancer by age 50 years ranged from 2.4% (95% CI, 2.4-2.4) in women with no PVs and no family history to 35.5% (95% CI, 21.6-55.1) in <jats:italic>PALB2</jats:italic> PV carriers with a family history. Among women who have not been diagnosed with breast cancer by age 50 years, the cumulative risk of breast cancer by age 80 years ranged from 11.1% (95% CI, 11.0-11.2) in noncarriers with no family history to 70.5% (95% CI, 52.8-83.5) for <jats:italic>PALB2</jats:italic> carriers with a family history. PV-specific cumulative risk estimates varied across subgroups defined by race and ethnicity and potentially modifiable epidemiologic risk factors.Conclusions and RelevanceIn this study, population-based estimates of cumulative breast cancer risk for established PVs, as informed by the CARRIERS case-control sample, varied by family history and potentially modifiable risk factors. These estimates provide guidance for identifying individuals who will most benefit from enhanced screening and prevention strategies.\",\"PeriodicalId\":14850,\"journal\":{\"name\":\"JAMA Oncology\",\"volume\":\"15 1\",\"pages\":\"\"},\"PeriodicalIF\":20.1000,\"publicationDate\":\"2025-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JAMA Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1001/jamaoncol.2025.3875\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAMA Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1001/jamaoncol.2025.3875","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

已知易感基因中的遗传致病性变异(PV)可大大增加乳腺癌风险,但PV状态、家族史和其他因素对美国普通人群乳腺癌风险的综合影响尚未得到很好的描述。目的通过乳腺癌一级家族史和其他因素对已确诊的pv患者进行总体和分层的人群乳腺癌风险评估。设计、环境和参与者本研究使用了13项美国乳腺癌病例对照研究的汇总数据,这些研究参与了与易感性相关的癌症风险评估(携带者)联盟。单个研究的入组时间为1976年至2013年,结果基于2023年3月发布的数据,分析时间为2022年6月至2025年7月。暴露、乳腺癌家族史、自我报告的种族和民族以及确定的危险因素。主要结果和测量方法从carrier联盟中估计了7个基因中pv的乳腺癌发病率比。使用个体化连贯绝对风险估计(iCARE)模型,将PV状态、发病率和死亡率统计数据结合起来,估计有条件累积乳腺癌风险和95% ci,按家族史分层并标准化到美国人群。还对纳入基于人群的数据和已公布的流行病学危险因素估计的模型进行了评估。结果共纳入67 692名女性,其中确诊乳腺癌患者33 841人。ATM、BRCA1、BRCA2、CHEK2和PALB2中的pv与乳腺癌风险密切相关,BRCA1和PALB2中的pv在家族史上表现出异质性。在考虑PV、家族史和既定危险因素的模型中,50岁时乳腺癌的累积风险估计范围从无PV和无家族史的女性的2.4% (95% CI, 2.4-2.4)到有家族史的PALB2 PV携带者的35.5% (95% CI, 21.6-55.1)。在50岁前未被诊断为乳腺癌的女性中,到80岁时乳腺癌的累积风险从无家族史的非携带者的11.1% (95% CI, 11.0-11.2)到有家族史的PALB2携带者的70.5% (95% CI, 52.8-83.5)不等。pv特异性累积风险估计在由种族和民族以及潜在可改变的流行病学风险因素定义的亚组中有所不同。结论和相关性在本研究中,根据携带者病例对照样本,基于人群的既定pv累积乳腺癌风险估计因家族史和潜在可改变的风险因素而异。这些估计为确定将从加强筛查和预防战略中获益最多的个人提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathogenic Variants, Family History, and Cumulative Risk of Breast Cancer in US Women
ImportanceInherited pathogenic variants (PVs) in known predisposition genes can greatly increase breast cancer risk, but the combined impact of PV status, family history, and other factors on breast cancer risk in the general US population has not been well described.ObjectiveTo evaluate population-based breast cancer risk estimates for those with established PVs overall and stratified by first-degree family history of breast cancer and other factors.Design, Setting, and ParticipantsThis study used pooled data from 13 US-based breast cancer case-control studies participating in the Cancer Risk Estimates Related to Susceptibility (CARRIERS) consortium. Enrollment for individual studies occurred between 1976 and 2013, and results are based on data released March 2023, with analyses conducted from June 2022 to July 2025.ExposuresPVs, breast cancer family history, self-reported race and ethnicity, and established risk factors.Main Outcomes and MeasuresBreast cancer rate ratios for PVs in 7 genes were estimated from the CARRIERS consortium. PV status and incidence and mortality statistics were combined using the Individualized Coherent Absolute Risk Estimation (iCARE) model to estimate conditional cumulative breast cancer risks and 95% CIs, stratified by family history and standardized to the US population. Models that incorporated population-based data and published estimates for established epidemiologic risk factors were also evaluated.ResultsA total of 67 692 women were studied, including 33 841 who were diagnosed with breast cancer. PVs in ATM, BRCA1, BRCA2, CHEK2, and PALB2 were strongly associated with breast cancer risk, with BRCA1 and PALB2 PVs showing evidence of heterogeneity by family history. In models considering PVs, family history, and established risk factors, the estimated cumulative risks of breast cancer by age 50 years ranged from 2.4% (95% CI, 2.4-2.4) in women with no PVs and no family history to 35.5% (95% CI, 21.6-55.1) in PALB2 PV carriers with a family history. Among women who have not been diagnosed with breast cancer by age 50 years, the cumulative risk of breast cancer by age 80 years ranged from 11.1% (95% CI, 11.0-11.2) in noncarriers with no family history to 70.5% (95% CI, 52.8-83.5) for PALB2 carriers with a family history. PV-specific cumulative risk estimates varied across subgroups defined by race and ethnicity and potentially modifiable epidemiologic risk factors.Conclusions and RelevanceIn this study, population-based estimates of cumulative breast cancer risk for established PVs, as informed by the CARRIERS case-control sample, varied by family history and potentially modifiable risk factors. These estimates provide guidance for identifying individuals who will most benefit from enhanced screening and prevention strategies.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
JAMA Oncology
JAMA Oncology Medicine-Oncology
自引率
1.80%
发文量
423
期刊介绍: JAMA Oncology is an international peer-reviewed journal that serves as the leading publication for scientists, clinicians, and trainees working in the field of oncology. It is part of the JAMA Network, a collection of peer-reviewed medical and specialty publications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信