Breast cancer risk associated with BRCA1 and BRCA2 pathogenic variants in the Eastern Chinese population

Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carrier...

Full description

Saved in:
Bibliographic Details
Published inCancer pathogenesis and therapy Vol. 3; no. 2; pp. 147 - 153
Main Authors Yu, Sanjian, Qiu, Xia, Wang, Zezhou, Xiao, Jialong, Ji, Hui, Shan, Hailin, Shao, Qing, Xia, Heng, Cao, Feng, Li, Jun, Fu, Cuixia, Chen, Liqin, Lu, Xiaofang, Su, Tingting, Yu, Qianqian, Hou, Shengqun, Wang, Honglian, Zheng, Ying, Shao, Zhimin, Liu, Yun, Hu, Zhen
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.03.2025
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carriers using a population-based breast cancer cohort from communities in Eastern China. Between July 2019 and March 2021, we tested 2216 breast cancer probands from Chinese communities for BRCA1/2 mutations and collected detailed information on the age, survival status, and malignancy history of first-degree relatives. The kin-cohort method was used to calculate the penetrance of breast cancer and other malignant tumors. Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 P/LP variants, 49 in the BRCA1 gene and 60 in the BRCA2 gene. The penetrance of female breast cancer by 85 years of age was 22.50% and 18.20% in BRCA1 and BRCA2 P/LP variant carriers, respectively. The penetrance of ovarian cancer by 85 years of age was 26.00% in BRCA1 P/LP variant carriers. The penetrance of other malignancies did not reach statistical significance owing to the small number of events. Our findings showed that breast cancer penetrance among BRCA1 and BRCA2 P/LP variant carriers was 22.50% and 18.20%, respectively, which suggests that prophylactic mastectomy may not be necessary for such Chinese individuals. ClinicalTrials.gov; https://clinicaltrials.gov/ct2/show/NCT04265937. [Display omitted] •The study investigated breast cancer gene 1/2 (BRCA1/2) mutation penetrance in the Eastern Chinese population.•Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 mutations.•Penetrance of breast cancer was 22.50% and 18.20% in BRCA1 and BRCA2 carriers, respectively.•The results suggest prophylactic mastectomy may not be necessary for BRCA1/2 carriers.•The findings provide new insights for breast cancer prevention in Chinese patients who are BRCA1/2 mutation carriers.
AbstractList Population-based penetrance studies of breast cancer gene 1/2 ( pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carriers using a population-based breast cancer cohort from communities in Eastern China. Between July 2019 and March 2021, we tested 2216 breast cancer probands from Chinese communities for mutations and collected detailed information on the age, survival status, and malignancy history of first-degree relatives. The kin-cohort method was used to calculate the penetrance of breast cancer and other malignant tumors. Of the 2216 breast cancer probands, 109 (4.90%) carried P/LP variants, 49 in the gene and 60 in the gene. The penetrance of female breast cancer by 85 years of age was 22.50% and 18.20% in and P/LP variant carriers, respectively. The penetrance of ovarian cancer by 85 years of age was 26.00% in P/LP variant carriers. The penetrance of other malignancies did not reach statistical significance owing to the small number of events. Our findings showed that breast cancer penetrance among and P/LP variant carriers was 22.50% and 18.20%, respectively, which suggests that prophylactic mastectomy may not be necessary for such Chinese individuals. ClinicalTrials.gov; https://clinicaltrials.gov/ct2/show/NCT04265937.
Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carriers using a population-based breast cancer cohort from communities in Eastern China. Between July 2019 and March 2021, we tested 2216 breast cancer probands from Chinese communities for BRCA1/2 mutations and collected detailed information on the age, survival status, and malignancy history of first-degree relatives. The kin-cohort method was used to calculate the penetrance of breast cancer and other malignant tumors. Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 P/LP variants, 49 in the BRCA1 gene and 60 in the BRCA2 gene. The penetrance of female breast cancer by 85 years of age was 22.50% and 18.20% in BRCA1 and BRCA2 P/LP variant carriers, respectively. The penetrance of ovarian cancer by 85 years of age was 26.00% in BRCA1 P/LP variant carriers. The penetrance of other malignancies did not reach statistical significance owing to the small number of events. Our findings showed that breast cancer penetrance among BRCA1 and BRCA2 P/LP variant carriers was 22.50% and 18.20%, respectively, which suggests that prophylactic mastectomy may not be necessary for such Chinese individuals. ClinicalTrials.gov; https://clinicaltrials.gov/ct2/show/NCT04265937. [Display omitted] •The study investigated breast cancer gene 1/2 (BRCA1/2) mutation penetrance in the Eastern Chinese population.•Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 mutations.•Penetrance of breast cancer was 22.50% and 18.20% in BRCA1 and BRCA2 carriers, respectively.•The results suggest prophylactic mastectomy may not be necessary for BRCA1/2 carriers.•The findings provide new insights for breast cancer prevention in Chinese patients who are BRCA1/2 mutation carriers.
Background: Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carriers using a population-based breast cancer cohort from communities in Eastern China. Methods: Between July 2019 and March 2021, we tested 2216 breast cancer probands from Chinese communities for BRCA1/2 mutations and collected detailed information on the age, survival status, and malignancy history of first-degree relatives. The kin-cohort method was used to calculate the penetrance of breast cancer and other malignant tumors. Results: Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 P/LP variants, 49 in the BRCA1 gene and 60 in the BRCA2 gene. The penetrance of female breast cancer by 85 years of age was 22.50% and 18.20% in BRCA1 and BRCA2 P/LP variant carriers, respectively. The penetrance of ovarian cancer by 85 years of age was 26.00% in BRCA1 P/LP variant carriers. The penetrance of other malignancies did not reach statistical significance owing to the small number of events. Conclusions: Our findings showed that breast cancer penetrance among BRCA1 and BRCA2 P/LP variant carriers was 22.50% and 18.20%, respectively, which suggests that prophylactic mastectomy may not be necessary for such Chinese individuals. Trial registration: ClinicalTrials.gov; https://clinicaltrials.gov/ct2/show/NCT04265937.
Image 1 • The study investigated breast cancer gene 1/2 (BRCA1/2) mutation penetrance in the Eastern Chinese population. • Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 mutations. • Penetrance of breast cancer was 22.50% and 18.20% in BRCA1 and BRCA2 carriers, respectively. • The results suggest prophylactic mastectomy may not be necessary for BRCA1 /2 carriers. • The findings provide new insights for breast cancer prevention in Chinese patients who are BRCA1/2 mutation carriers.
Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carriers using a population-based breast cancer cohort from communities in Eastern China.BackgroundPopulation-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently lacking; thus, we aimed to investigate the penetrance of breast cancer and other malignant tumors among BRCA1/2 P/LP variant carriers using a population-based breast cancer cohort from communities in Eastern China.Between July 2019 and March 2021, we tested 2216 breast cancer probands from Chinese communities for BRCA1/2 mutations and collected detailed information on the age, survival status, and malignancy history of first-degree relatives. The kin-cohort method was used to calculate the penetrance of breast cancer and other malignant tumors.MethodsBetween July 2019 and March 2021, we tested 2216 breast cancer probands from Chinese communities for BRCA1/2 mutations and collected detailed information on the age, survival status, and malignancy history of first-degree relatives. The kin-cohort method was used to calculate the penetrance of breast cancer and other malignant tumors.Of the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 P/LP variants, 49 in the BRCA1 gene and 60 in the BRCA2 gene. The penetrance of female breast cancer by 85 years of age was 22.50% and 18.20% in BRCA1 and BRCA2 P/LP variant carriers, respectively. The penetrance of ovarian cancer by 85 years of age was 26.00% in BRCA1 P/LP variant carriers. The penetrance of other malignancies did not reach statistical significance owing to the small number of events.ResultsOf the 2216 breast cancer probands, 109 (4.90%) carried BRCA1/2 P/LP variants, 49 in the BRCA1 gene and 60 in the BRCA2 gene. The penetrance of female breast cancer by 85 years of age was 22.50% and 18.20% in BRCA1 and BRCA2 P/LP variant carriers, respectively. The penetrance of ovarian cancer by 85 years of age was 26.00% in BRCA1 P/LP variant carriers. The penetrance of other malignancies did not reach statistical significance owing to the small number of events.Our findings showed that breast cancer penetrance among BRCA1 and BRCA2 P/LP variant carriers was 22.50% and 18.20%, respectively, which suggests that prophylactic mastectomy may not be necessary for such Chinese individuals.ConclusionsOur findings showed that breast cancer penetrance among BRCA1 and BRCA2 P/LP variant carriers was 22.50% and 18.20%, respectively, which suggests that prophylactic mastectomy may not be necessary for such Chinese individuals.ClinicalTrials.gov; https://clinicaltrials.gov/ct2/show/NCT04265937.Trial registrationClinicalTrials.gov; https://clinicaltrials.gov/ct2/show/NCT04265937.
Author Su, Tingting
Xia, Heng
Wang, Zezhou
Lu, Xiaofang
Wang, Honglian
Chen, Liqin
Hu, Zhen
Shao, Qing
Shan, Hailin
Zheng, Ying
Liu, Yun
Qiu, Xia
Li, Jun
Fu, Cuixia
Cao, Feng
Shao, Zhimin
Yu, Qianqian
Hou, Shengqun
Xiao, Jialong
Yu, Sanjian
Ji, Hui
Author_xml – sequence: 1
  givenname: Sanjian
  surname: Yu
  fullname: Yu, Sanjian
  organization: Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China
– sequence: 2
  givenname: Xia
  surname: Qiu
  fullname: Qiu, Xia
  organization: Department of Breast Surgery, Zhoushan Hospital, Zhoushan, Zhejiang 31600, China
– sequence: 3
  givenname: Zezhou
  surname: Wang
  fullname: Wang, Zezhou
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 4
  givenname: Jialong
  surname: Xiao
  fullname: Xiao, Jialong
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 5
  givenname: Hui
  surname: Ji
  fullname: Ji, Hui
  organization: Department of General Surgery, Shanghai Tenth People's Hospital, Chongming Branch, Shanghai 202157, China
– sequence: 6
  givenname: Hailin
  surname: Shan
  fullname: Shan, Hailin
  organization: Department of Thyroid and Breast Surgery, Jiangyin People's Hospital, Southeast University, Jiangyin, Jiangsu 214499, China
– sequence: 7
  givenname: Qing
  surname: Shao
  fullname: Shao, Qing
  organization: Department of Thyroid and Breast Surgery, Jiangyin People's Hospital, Southeast University, Jiangyin, Jiangsu 214499, China
– sequence: 8
  givenname: Heng
  surname: Xia
  fullname: Xia, Heng
  organization: Department of Thyroid and Breast Surgery, Shaoxing Central Hospital, Shaoxing, Zhejiang 312030, China
– sequence: 9
  givenname: Feng
  surname: Cao
  fullname: Cao, Feng
  organization: Department of General Surgery, Shanghai Seventh People's Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200137, China
– sequence: 10
  givenname: Jun
  surname: Li
  fullname: Li, Jun
  organization: Department of General Surgery, Shanghai Pudong New Area Gongli Hospital, Shanghai 200135, China
– sequence: 11
  givenname: Cuixia
  surname: Fu
  fullname: Fu, Cuixia
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 12
  givenname: Liqin
  surname: Chen
  fullname: Chen, Liqin
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 13
  givenname: Xiaofang
  surname: Lu
  fullname: Lu, Xiaofang
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 14
  givenname: Tingting
  surname: Su
  fullname: Su, Tingting
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 15
  givenname: Qianqian
  surname: Yu
  fullname: Yu, Qianqian
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 16
  givenname: Shengqun
  surname: Hou
  fullname: Hou, Shengqun
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 17
  givenname: Honglian
  surname: Wang
  fullname: Wang, Honglian
  organization: AITA Biomedical Research Institute, Shanghai 201101, China
– sequence: 18
  givenname: Ying
  surname: Zheng
  fullname: Zheng, Ying
  organization: Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China
– sequence: 19
  givenname: Zhimin
  surname: Shao
  fullname: Shao, Zhimin
  organization: Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China
– sequence: 20
  givenname: Yun
  surname: Liu
  fullname: Liu, Yun
  organization: Department of Biliary and Pancreatic Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China
– sequence: 21
  givenname: Zhen
  orcidid: 0000-0001-8227-5056
  surname: Hu
  fullname: Hu, Zhen
  email: zhenhu@fudan.edu.cn
  organization: Department of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/40182128$$D View this record in MEDLINE/PubMed
BookMark eNqFUk1vEzEQXaEiWkp_ABfkI5cEf613LQ6ojQpUqoQE3K2JdzbrdGsvtpOq_x43KVXbQ5Ge5JH93puR572tDnzwWFXvGZ0zytSn9dxOec4pl3NaQPmr6ohrqWcNE_zgUX1YnaS0poWhOacNfVMdSspaznh7VA1nESFlYsFbjCS6dEUgpWAdZOzIjcsDOfu5OGUEfLerOJkgD2GF3lmyhejA50ScJ3lAcl68MHqyGJzHhGQK02aE7IJ_V73uYUx4cn8eV7--nv9efJ9d_vh2sTi9nFkl2jxrbEtbYSVTqukKWKtai6qRrG6WDQjLKe20QmH7urZKs75w0YJcAu-ZOK4u9q5dgLWZoruGeGsCOLO7CHFlIGZnRzRSUg096r5GJmXXaC6FYrLWQMWSK1m8vuy9ps3yGjuLPkcYn5g-ffFuMKuwNYxpJcrgxeHjvUMMfzaYsrl2yeI4gsewSWZHqmtai0L98LjZQ5d_myoEtifYGFKK2D9QGDV3gTBrUwJh7gJhaAHlRdM801iXd9so87rxReXnvRLLqrYOo0nWYYlI5yLaXH7TvajWz9R2dCUuMF7h7X-0fwF4F-Gm
CitedBy_id crossref_primary_10_1016_j_cpt_2024_06_006
crossref_primary_10_1186_s12957_024_03553_9
Cites_doi 10.1056/NEJMra1503523
10.1093/jnci/94.16.1221
10.1093/jnci/djj465
10.1200/JCO.2005.03.6772
10.1016/j.ygyno.2011.01.020
10.1086/375033
10.1016/j.jncc.2020.12.001
10.1007/s10549-007-9708-3
10.1001/jama.2017.7112
10.1056/NEJMoa2005936
10.1093/aje/148.7.623
10.1038/87876
10.1001/jama.2007.55-a
10.1200/JCO.21.02112
10.21037/pcm-22-36
10.1093/jnci/djr114
10.1111/j.0006-341X.2001.00245.x
10.1001/jama.2014.5985
10.1073/pnas.1415979111
10.1002/ijc.32176
10.1097/IGC.0000000000001065
10.1093/jnci/djj012
10.1186/s13045-020-01010-0
10.1200/JCO.2013.51.4661
10.1007/s10549-016-3766-3
10.18632/oncotarget.24382
10.1530/ERC-16-0277
ContentType Journal Article
Copyright 2024 The Authors
2024 The Authors.
2024 The Authors 2024
Copyright_xml – notice: 2024 The Authors
– notice: 2024 The Authors.
– notice: 2024 The Authors 2024
DBID 6I.
AAFTH
AAYXX
CITATION
NPM
7X8
5PM
DOA
DOI 10.1016/j.cpt.2024.04.002
DatabaseName ScienceDirect Open Access Titles
Elsevier:ScienceDirect:Open Access
CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList PubMed




MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: Directory of Open Access Journals (DOAJ)
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2949-7132
EndPage 153
ExternalDocumentID oai_doaj_org_article_4409afe9f5e144d7924361459a03b264
PMC11963186
40182128
10_1016_j_cpt_2024_04_002
S2949713224000260
Genre Journal Article
GroupedDBID .1-
.FO
0R~
AALRI
AAXUO
AAYWO
ACVFH
ADCNI
ADVLN
AEUPX
AEXQZ
AFJKZ
AFPUW
AFRHN
AIGII
AITUG
AJUYK
AKBMS
AKRWK
AKYEP
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
APXCP
EBS
FDB
GROUPED_DOAJ
M41
PGMZT
ROL
RPM
Z5R
6I.
AAFTH
AFCTW
AAYXX
CITATION
NPM
7X8
5PM
ID FETCH-LOGICAL-c638t-7c8083c41667d67d1868ce674157b7a3c200d96e3cf55c691fc41eca4ba2f13
IEDL.DBID DOA
ISSN 2949-7132
2097-2563
IngestDate Wed Aug 27 01:30:29 EDT 2025
Thu Aug 21 18:38:45 EDT 2025
Fri Jul 11 18:51:07 EDT 2025
Sun Apr 06 01:22:40 EDT 2025
Thu Apr 24 23:07:16 EDT 2025
Tue Jul 01 05:20:45 EDT 2025
Sat Mar 22 15:53:47 EDT 2025
Tue Aug 26 19:07:40 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords Chinese population
Breast cancer
BRCA1/2 gene mutations
Population-based studies
Language English
License This is an open access article under the CC BY-NC-ND license.
2024 The Authors.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c638t-7c8083c41667d67d1868ce674157b7a3c200d96e3cf55c691fc41eca4ba2f13
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Sanjian Yu and Xia Qiu contributed equally to this work.
ORCID 0000-0001-8227-5056
OpenAccessLink https://doaj.org/article/4409afe9f5e144d7924361459a03b264
PMID 40182128
PQID 3186355053
PQPubID 23479
PageCount 7
ParticipantIDs doaj_primary_oai_doaj_org_article_4409afe9f5e144d7924361459a03b264
pubmedcentral_primary_oai_pubmedcentral_nih_gov_11963186
proquest_miscellaneous_3186355053
pubmed_primary_40182128
crossref_primary_10_1016_j_cpt_2024_04_002
crossref_citationtrail_10_1016_j_cpt_2024_04_002
elsevier_sciencedirect_doi_10_1016_j_cpt_2024_04_002
elsevier_clinicalkey_doi_10_1016_j_cpt_2024_04_002
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2025-03-01
PublicationDateYYYYMMDD 2025-03-01
PublicationDate_xml – month: 03
  year: 2025
  text: 2025-03-01
  day: 01
PublicationDecade 2020
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Cancer pathogenesis and therapy
PublicationTitleAlternate Cancer Pathog Ther
PublicationYear 2025
Publisher Elsevier B.V
Elsevier
Publisher_xml – name: Elsevier B.V
– name: Elsevier
References Milne, Antoniou (bib7) 2016; 23
Gabai-Kapara, Lahad, Kaufman (bib5) 2014; 111
Wu, Wu, Kong (bib25) 2017; 27
Mai, Garceau, Graubard (bib30) 2011; 103
Nathanson, Wooster, Weber (bib1) 2001; 7
Chatterjee, Wacholder (bib17) 2001; 57
Zhang, Shin, Chai (bib13) 2018; 9
Li, Hu, Rao (bib9) 2008; 110
Rebbeck, Mitra, Wan (bib32) 2015; 313
Hu, Hart, Gnanaolivu (bib22) 2021; 384
Chen, Iversen, Friebel (bib4) 2006; 24
Hartmann, Lindor (bib6) 2016; 374
Kuchenbaecker, Hopper, Barnes (bib24) 2017; 317
Yang, Wu, Lu (bib10) 2015; 10
Liu, Wang, Wang (bib12) 2021; 14
Wacholder, Hartge, Struewing (bib18) 1998; 148
Li, Silvestri, Leslie (bib28) 2022; 40
Zhang, Royer, Li (bib27) 2011; 121
Begg, Haile, Borg (bib3) 2008; 299
Begg (bib15) 2002; 94
Zhang, Sun, Zheng (bib8) 2021; 1
(bib20) 2021
(bib21) 2013
Antoniou, Pharoah, Narod (bib2) 2003; 72
Bhaskaran, Chandratre, Gupta (bib11) 2019; 145
Yao, Sun, Zhang (bib14) 2016; 156
Wang, Yu, Feng (bib16) 2022; 5
(bib19) 2017
(bib29) 2019
Wood, Kadlubek, Pham (bib31) 2014; 32
Tryggvadottir, Sigvaldason, Olafsdottir (bib23) 2006; 98
Risch, McLaughlin, Cole (bib26) 2006; 98
Zhang (10.1016/j.cpt.2024.04.002_bib27) 2011; 121
Liu (10.1016/j.cpt.2024.04.002_bib12) 2021; 14
Yao (10.1016/j.cpt.2024.04.002_bib14) 2016; 156
Li (10.1016/j.cpt.2024.04.002_bib9) 2008; 110
Chatterjee (10.1016/j.cpt.2024.04.002_bib17) 2001; 57
Hartmann (10.1016/j.cpt.2024.04.002_bib6) 2016; 374
Li (10.1016/j.cpt.2024.04.002_bib28) 2022; 40
Wood (10.1016/j.cpt.2024.04.002_bib31) 2014; 32
Bhaskaran (10.1016/j.cpt.2024.04.002_bib11) 2019; 145
(10.1016/j.cpt.2024.04.002_bib20) 2021
(10.1016/j.cpt.2024.04.002_bib21) 2013
Tryggvadottir (10.1016/j.cpt.2024.04.002_bib23) 2006; 98
Begg (10.1016/j.cpt.2024.04.002_bib15) 2002; 94
Begg (10.1016/j.cpt.2024.04.002_bib3) 2008; 299
(10.1016/j.cpt.2024.04.002_bib29) 2019
Mai (10.1016/j.cpt.2024.04.002_bib30) 2011; 103
(10.1016/j.cpt.2024.04.002_bib19) 2017
Milne (10.1016/j.cpt.2024.04.002_bib7) 2016; 23
Wu (10.1016/j.cpt.2024.04.002_bib25) 2017; 27
Rebbeck (10.1016/j.cpt.2024.04.002_bib32) 2015; 313
Chen (10.1016/j.cpt.2024.04.002_bib4) 2006; 24
Kuchenbaecker (10.1016/j.cpt.2024.04.002_bib24) 2017; 317
Wacholder (10.1016/j.cpt.2024.04.002_bib18) 1998; 148
Yang (10.1016/j.cpt.2024.04.002_bib10) 2015; 10
Gabai-Kapara (10.1016/j.cpt.2024.04.002_bib5) 2014; 111
Nathanson (10.1016/j.cpt.2024.04.002_bib1) 2001; 7
Antoniou (10.1016/j.cpt.2024.04.002_bib2) 2003; 72
Risch (10.1016/j.cpt.2024.04.002_bib26) 2006; 98
Zhang (10.1016/j.cpt.2024.04.002_bib8) 2021; 1
Zhang (10.1016/j.cpt.2024.04.002_bib13) 2018; 9
Hu (10.1016/j.cpt.2024.04.002_bib22) 2021; 384
Wang (10.1016/j.cpt.2024.04.002_bib16) 2022; 5
References_xml – volume: 9
  start-page: 25025
  year: 2018
  end-page: 25033
  ident: bib13
  article-title: Breast and ovarian cancer penetrance of BRCA1/2 mutations among Hong Kong women
  publication-title: Oncotarget
– volume: 317
  start-page: 2402
  year: 2017
  end-page: 2416
  ident: bib24
  article-title: Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
  publication-title: JAMA
– volume: 98
  start-page: 1694
  year: 2006
  end-page: 1706
  ident: bib26
  article-title: Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: A kin-cohort study in Ontario, Canada
  publication-title: J Natl Cancer Inst
– volume: 94
  start-page: 1221
  year: 2002
  end-page: 1226
  ident: bib15
  article-title: On the use of familial aggregation in population-based case probands for calculating penetrance
  publication-title: J Natl Cancer Inst
– volume: 57
  start-page: 245
  year: 2001
  end-page: 252
  ident: bib17
  article-title: A marginal likelihood approach for estimating penetrance from kin-cohort designs
  publication-title: Biometrics
– volume: 98
  start-page: 116
  year: 2006
  end-page: 122
  ident: bib23
  article-title: Population-based study of changing breast cancer risk in Icelandic BRCA2 mutation carriers, 1920–2000
  publication-title: J Natl Cancer Inst
– volume: 111
  start-page: 14205
  year: 2014
  end-page: 14210
  ident: bib5
  article-title: Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2
  publication-title: Proc Natl Acad Sci U S A
– volume: 24
  start-page: 863
  year: 2006
  end-page: 871
  ident: bib4
  article-title: Characterization of BRCA1 and BRCA2 mutations in a large United States sample
  publication-title: J Clin Oncol
– year: 2021
  ident: bib20
  publication-title: Hong Kong Female Breast Cancer in 2019: Hong Kong Cancer Registry
– volume: 313
  start-page: 1347
  year: 2015
  end-page: 1361
  ident: bib32
  article-title: Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
  publication-title: JAMA
– volume: 72
  start-page: 1117
  year: 2003
  end-page: 1130
  ident: bib2
  article-title: Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
  publication-title: Am J Hum Genet
– volume: 110
  start-page: 99
  year: 2008
  end-page: 109
  ident: bib9
  article-title: The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: Two recurrent mutations were identified
  publication-title: Breast Cancer Res Treat
– volume: 156
  start-page: 441
  year: 2016
  end-page: 445
  ident: bib14
  article-title: Breast cancer risk in Chinese women with BRCA1 or BRCA2 mutations
  publication-title: Breast Cancer Res Treat
– volume: 1
  start-page: 2
  year: 2021
  end-page: 11
  ident: bib8
  article-title: Cancer incidence and mortality in China, 2015
  publication-title: J Natl Cancer Cent
– volume: 384
  start-page: 440
  year: 2021
  end-page: 451
  ident: bib22
  article-title: A population-based study of genes previously implicated in breast cancer
  publication-title: N Engl J Med
– volume: 103
  start-page: 788
  year: 2011
  end-page: 797
  ident: bib30
  article-title: Confirmation of family cancer history reported in a population-based survey
  publication-title: J Natl Cancer Inst
– year: 2013
  ident: bib21
  publication-title: Beijing Municipal People’s Government. Beijing municipal health and population health report
– volume: 7
  start-page: 552
  year: 2001
  end-page: 556
  ident: bib1
  article-title: Breast cancer genetics: What we know and what we need
  publication-title: Nat Med
– year: 2019
  ident: bib29
  article-title: Familial breast cancer: Classification, care and managing breast cancer and related risks in people with a family history of breast cancer
– volume: 145
  start-page: 962
  year: 2019
  end-page: 973
  ident: bib11
  article-title: Germline variation in BRCA1/2 is highly ethnic-specific: Evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients
  publication-title: Int J Cancer
– volume: 27
  start-page: 1650
  year: 2017
  end-page: 1657
  ident: bib25
  article-title: The first nationwide multicenter prevalence study of germline BRCA1 and BRCA2 mutations in Chinese ovarian cancer patients
  publication-title: Int J Gynecol Cancer
– volume: 14
  start-page: 18
  year: 2021
  ident: bib12
  article-title: Prevalence and reclassification of BRCA1 and BRCA2 variants in a large, unselected Chinese Han breast cancer cohort
  publication-title: J Hematol Oncol
– volume: 299
  start-page: 194
  year: 2008
  end-page: 201
  ident: bib3
  article-title: Variation of breast cancer risk among BRCA1/2 carriers
  publication-title: JAMA
– volume: 374
  start-page: 454
  year: 2016
  end-page: 468
  ident: bib6
  article-title: The role of risk-reducing surgery in hereditary breast and ovarian cancer
  publication-title: N Engl J Med
– volume: 32
  start-page: 824
  year: 2014
  end-page: 829
  ident: bib31
  article-title: Quality of cancer family history and referral for genetic counseling and testing among oncology practices: A pilot test of quality measures as part of the American Society of Clinical Oncology Quality Oncology Practice Initiative
  publication-title: J Clin Oncol
– volume: 121
  start-page: 353
  year: 2011
  end-page: 357
  ident: bib27
  article-title: Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer
  publication-title: Gynecol Oncol
– volume: 5
  start-page: 36
  year: 2022
  ident: bib16
  article-title: Protocol: Screening of genetic susceptibility genes for breast cancer patients and establishment of genetic high-risk populations cohort in east china communities
  publication-title: Precis Cancer Med
– volume: 148
  start-page: 623
  year: 1998
  end-page: 630
  ident: bib18
  article-title: The kin-cohort study for estimating penetrance
  publication-title: Am J Epidemiol
– year: 2017
  ident: bib19
  article-title: Shanghai cancer report 2017. Shanghai Municipal Center for Disease Control and Prevention Scientific Report
– volume: 23
  start-page: T69
  year: 2016
  end-page: T84
  ident: bib7
  article-title: Modifiers of breast and ovarian cancer risks for BRCA1 and BRCA2 mutation carriers
  publication-title: Endocr Relat Cancer
– volume: 40
  start-page: 1529
  year: 2022
  end-page: 1541
  ident: bib28
  article-title: Cancer risks associated with BRCA1 and BRCA2 pathogenic variants
  publication-title: J Clin Oncol
– volume: 10
  year: 2015
  ident: bib10
  article-title: Identification of a comprehensive spectrum of genetic factors for hereditary breast cancer in a Chinese population by next-generation sequencing
  publication-title: PLoS One
– volume: 374
  start-page: 454
  year: 2016
  ident: 10.1016/j.cpt.2024.04.002_bib6
  article-title: The role of risk-reducing surgery in hereditary breast and ovarian cancer
  publication-title: N Engl J Med
  doi: 10.1056/NEJMra1503523
– volume: 94
  start-page: 1221
  year: 2002
  ident: 10.1016/j.cpt.2024.04.002_bib15
  article-title: On the use of familial aggregation in population-based case probands for calculating penetrance
  publication-title: J Natl Cancer Inst
  doi: 10.1093/jnci/94.16.1221
– volume: 98
  start-page: 1694
  year: 2006
  ident: 10.1016/j.cpt.2024.04.002_bib26
  article-title: Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: A kin-cohort study in Ontario, Canada
  publication-title: J Natl Cancer Inst
  doi: 10.1093/jnci/djj465
– volume: 24
  start-page: 863
  year: 2006
  ident: 10.1016/j.cpt.2024.04.002_bib4
  article-title: Characterization of BRCA1 and BRCA2 mutations in a large United States sample
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2005.03.6772
– volume: 121
  start-page: 353
  year: 2011
  ident: 10.1016/j.cpt.2024.04.002_bib27
  article-title: Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer
  publication-title: Gynecol Oncol
  doi: 10.1016/j.ygyno.2011.01.020
– volume: 72
  start-page: 1117
  year: 2003
  ident: 10.1016/j.cpt.2024.04.002_bib2
  article-title: Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies
  publication-title: Am J Hum Genet
  doi: 10.1086/375033
– volume: 1
  start-page: 2
  year: 2021
  ident: 10.1016/j.cpt.2024.04.002_bib8
  article-title: Cancer incidence and mortality in China, 2015
  publication-title: J Natl Cancer Cent
  doi: 10.1016/j.jncc.2020.12.001
– volume: 110
  start-page: 99
  year: 2008
  ident: 10.1016/j.cpt.2024.04.002_bib9
  article-title: The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: Two recurrent mutations were identified
  publication-title: Breast Cancer Res Treat
  doi: 10.1007/s10549-007-9708-3
– volume: 317
  start-page: 2402
  year: 2017
  ident: 10.1016/j.cpt.2024.04.002_bib24
  article-title: Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
  publication-title: JAMA
  doi: 10.1001/jama.2017.7112
– volume: 384
  start-page: 440
  year: 2021
  ident: 10.1016/j.cpt.2024.04.002_bib22
  article-title: A population-based study of genes previously implicated in breast cancer
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa2005936
– volume: 148
  start-page: 623
  year: 1998
  ident: 10.1016/j.cpt.2024.04.002_bib18
  article-title: The kin-cohort study for estimating penetrance
  publication-title: Am J Epidemiol
  doi: 10.1093/aje/148.7.623
– volume: 7
  start-page: 552
  year: 2001
  ident: 10.1016/j.cpt.2024.04.002_bib1
  article-title: Breast cancer genetics: What we know and what we need
  publication-title: Nat Med
  doi: 10.1038/87876
– volume: 299
  start-page: 194
  year: 2008
  ident: 10.1016/j.cpt.2024.04.002_bib3
  article-title: Variation of breast cancer risk among BRCA1/2 carriers
  publication-title: JAMA
  doi: 10.1001/jama.2007.55-a
– volume: 40
  start-page: 1529
  year: 2022
  ident: 10.1016/j.cpt.2024.04.002_bib28
  article-title: Cancer risks associated with BRCA1 and BRCA2 pathogenic variants
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.21.02112
– volume: 5
  start-page: 36
  year: 2022
  ident: 10.1016/j.cpt.2024.04.002_bib16
  article-title: Protocol: Screening of genetic susceptibility genes for breast cancer patients and establishment of genetic high-risk populations cohort in east china communities
  publication-title: Precis Cancer Med
  doi: 10.21037/pcm-22-36
– year: 2021
  ident: 10.1016/j.cpt.2024.04.002_bib20
– volume: 103
  start-page: 788
  year: 2011
  ident: 10.1016/j.cpt.2024.04.002_bib30
  article-title: Confirmation of family cancer history reported in a population-based survey
  publication-title: J Natl Cancer Inst
  doi: 10.1093/jnci/djr114
– volume: 57
  start-page: 245
  year: 2001
  ident: 10.1016/j.cpt.2024.04.002_bib17
  article-title: A marginal likelihood approach for estimating penetrance from kin-cohort designs
  publication-title: Biometrics
  doi: 10.1111/j.0006-341X.2001.00245.x
– volume: 10
  year: 2015
  ident: 10.1016/j.cpt.2024.04.002_bib10
  article-title: Identification of a comprehensive spectrum of genetic factors for hereditary breast cancer in a Chinese population by next-generation sequencing
  publication-title: PLoS One
– year: 2017
  ident: 10.1016/j.cpt.2024.04.002_bib19
– volume: 313
  start-page: 1347
  year: 2015
  ident: 10.1016/j.cpt.2024.04.002_bib32
  article-title: Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
  publication-title: JAMA
  doi: 10.1001/jama.2014.5985
– volume: 111
  start-page: 14205
  year: 2014
  ident: 10.1016/j.cpt.2024.04.002_bib5
  article-title: Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1415979111
– volume: 145
  start-page: 962
  year: 2019
  ident: 10.1016/j.cpt.2024.04.002_bib11
  article-title: Germline variation in BRCA1/2 is highly ethnic-specific: Evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients
  publication-title: Int J Cancer
  doi: 10.1002/ijc.32176
– volume: 27
  start-page: 1650
  year: 2017
  ident: 10.1016/j.cpt.2024.04.002_bib25
  article-title: The first nationwide multicenter prevalence study of germline BRCA1 and BRCA2 mutations in Chinese ovarian cancer patients
  publication-title: Int J Gynecol Cancer
  doi: 10.1097/IGC.0000000000001065
– volume: 98
  start-page: 116
  year: 2006
  ident: 10.1016/j.cpt.2024.04.002_bib23
  article-title: Population-based study of changing breast cancer risk in Icelandic BRCA2 mutation carriers, 1920–2000
  publication-title: J Natl Cancer Inst
  doi: 10.1093/jnci/djj012
– volume: 14
  start-page: 18
  year: 2021
  ident: 10.1016/j.cpt.2024.04.002_bib12
  article-title: Prevalence and reclassification of BRCA1 and BRCA2 variants in a large, unselected Chinese Han breast cancer cohort
  publication-title: J Hematol Oncol
  doi: 10.1186/s13045-020-01010-0
– volume: 32
  start-page: 824
  year: 2014
  ident: 10.1016/j.cpt.2024.04.002_bib31
  article-title: Quality of cancer family history and referral for genetic counseling and testing among oncology practices: A pilot test of quality measures as part of the American Society of Clinical Oncology Quality Oncology Practice Initiative
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2013.51.4661
– volume: 156
  start-page: 441
  year: 2016
  ident: 10.1016/j.cpt.2024.04.002_bib14
  article-title: Breast cancer risk in Chinese women with BRCA1 or BRCA2 mutations
  publication-title: Breast Cancer Res Treat
  doi: 10.1007/s10549-016-3766-3
– year: 2013
  ident: 10.1016/j.cpt.2024.04.002_bib21
– year: 2019
  ident: 10.1016/j.cpt.2024.04.002_bib29
– volume: 9
  start-page: 25025
  year: 2018
  ident: 10.1016/j.cpt.2024.04.002_bib13
  article-title: Breast and ovarian cancer penetrance of BRCA1/2 mutations among Hong Kong women
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.24382
– volume: 23
  start-page: T69
  year: 2016
  ident: 10.1016/j.cpt.2024.04.002_bib7
  article-title: Modifiers of breast and ovarian cancer risks for BRCA1 and BRCA2 mutation carriers
  publication-title: Endocr Relat Cancer
  doi: 10.1530/ERC-16-0277
SSID ssj0002922070
ssib058688316
ssib051085483
Score 2.3110797
Snippet Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are...
Population-based penetrance studies of breast cancer gene 1/2 ( pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese population are currently...
Image 1 • The study investigated breast cancer gene 1/2 (BRCA1/2) mutation penetrance in the Eastern Chinese population. • Of the 2216 breast cancer probands,...
Background: Population-based penetrance studies of breast cancer gene 1/2 (BRCA1/2) pathogenic or likely pathogenic (P/LP) variants in the Eastern Chinese...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
elsevier
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 147
SubjectTerms BRCA1/2 gene mutations
Breast cancer
Chinese population
Population-based studies
Title Breast cancer risk associated with BRCA1 and BRCA2 pathogenic variants in the Eastern Chinese population
URI https://www.clinicalkey.com/#!/content/1-s2.0-S2949713224000260
https://dx.doi.org/10.1016/j.cpt.2024.04.002
https://www.ncbi.nlm.nih.gov/pubmed/40182128
https://www.proquest.com/docview/3186355053
https://pubmed.ncbi.nlm.nih.gov/PMC11963186
https://doaj.org/article/4409afe9f5e144d7924361459a03b264
Volume 3
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1NT9wwELUqDhUX1BZKQ1tkpJ4qRd11nNg5sgiEkOBAW4mbZU_GYqsqu4KF38-M86HdVoILUg5R1k42nvHMG3vyRohvdYimhBBzo0ORa63rPNiIOVhbIYYGVOSPky-vqvPf-uKmvFkr9cU5YR09cDdwPzQFID5iHUsk7N8YihcKcill7SdFIG_O1pd83lowxTZY1UqRMg_bmCmhC5acO6l0ojbtl1EGR5T4-jf80f9489-0yTU_dPZO7PQAUh53f_y9eIPtB_H2st8i3xW3M04zX0lgcd5JTh2XvpcBNpLXXeXs-uR4Kn3bpDMluSzxgjRpDvKRYmdOjZHzVhI2lKc-MSlIrrON9yiXY8GvPfHz7PTXyXnel1PIgSbZKjdgCW8BIbDKNHQwUT5gxZDCBOMLoAnT1BUWEMsSqnoaqS2C18GrOC0-iq120eInIctCU9QUlcEadDA2WJJzEyJUGLFsYiYmw8g66JnGueDFXzeklP1xJAzHwnATOiYqE9_HLsuOZuO5xjMW19iQGbLTBdIb1-uNe0lvMqEGYbvhI1Qym3Sj-XNP1mOnHqF0yOOlbkeDNjmavbwl41tcPNw7sqiM-MgSZmK_067xtSjytQQsbCbsht5tvPfmL-38NjGET9mu0q0PXmOkPottxUWPU-LdF7G1unvAr4TEVuEwTbrDtET2BFWyMPs
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Breast+cancer+risk+associated+with+BRCA1+and+BRCA2+pathogenic+variants+in+the+Eastern+Chinese+population&rft.jtitle=Cancer+pathogenesis+and+therapy&rft.au=Sanjian+Yu&rft.au=Xia+Qiu&rft.au=Zezhou+Wang&rft.au=Jialong+Xiao&rft.date=2025-03-01&rft.pub=Elsevier&rft.eissn=2949-7132&rft.volume=3&rft.issue=2&rft.spage=147&rft.epage=153&rft_id=info:doi/10.1016%2Fj.cpt.2024.04.002&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_4409afe9f5e144d7924361459a03b264
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2949-7132&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2949-7132&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2949-7132&client=summon