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Breast Cancer Family Registry Cohort (BCFR)
Breast Cancer Family Registry Cohort logo
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Sample details

The BCFR is a multi-center prospective cohort comprised of over 30,000 women and men from nearly 12,000 families from the United States, Canada, and Australia. BCFR aims to facilitate research investigating new ways to prevent, diagnose, and treat cancer. Participants were recruited from six international research sites and included people with breast cancer or a family history of breast cancer, their relatives and healthy controls. There have been several follow-ups since initial baseline data collection from 1996 to 2011 and three sub-studies associated with the cohort: Young Women’s Study, ProF-SC: Prospective Family Study Cohort, and the LEGACY Girls Study.

Study design
Cohort - open, Registry

Number of participants at first data collection

32,726 (participants)

Recruitment is ongoing

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Cancer patients
Control participants
Family members
Racial and ethnic minorities
Dataset details
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Countries

Australia, Canada, United States of America

Year of first data collection

1996

Primary Institutions

Columbia University

Lunenfeld-Tanenbaum Research Institute (LTRI)

Stanford University

Temple University

University of Melbourne

Links

bcfamilyregistry.org/

cedcd.nci.nih.gov/cohort

ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi

Profile paper DOI

doi.org/10.1186/bcr801

Funders

National Cancer Institute (NCI)

National Institutes of Health (NIH)

U.S. Department of Health and Human Services (DHHS)

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – online
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Breast cancer
    Cancer registry
    Diet and nutrition
    Ethnic minorities
    Family health history
    Genetics
    International collaboration
    Racial minorities
    Sub-studies

    Consortia and dataset groups

    Breast Cancer Family Registry (BCFR)
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