CoF-AT - French Cohort Study on Ataxia Telangiectasia

Head :
Andrieu Nadine, U900
Stoppa-Lyonnet , U900

Last update : 07/08/2015 | Version : 2 | ID : 60031

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Métadonnées
Identification
General Aspects
Scientific investigator(s) (Contact)
Collaborations
Funding
Governance of the database
Additional contact
Type of database
Database objective
Population type
Dates
Size of the database
Data
Procedures
Promotion
Access
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General
Identification
Detailed name French Cohort Study on Ataxia Telangiectasia
Sign or acronym CoF-AT
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation Avis CCPRB n°1989 du 26/07/2002, avis CNIL n°902310 du 30/12/2002, Avis CCTIS n°02.256 du 04/09/2002
General Aspects
Medical area Cancer research
Health determinants Genetic
Keywords Health episodes, cancer, environment
Scientific investigator(s) (Contact)
Name of the director Andrieu
Surname Nadine
Phone +33 (0)1 72 38 93 83
Email nadine.andrieu@curie.net
Unit U900
Organization INSERM
Name of the director Stoppa-Lyonnet
Unit U900
Organization INSERM
Collaborations
Participation in projects, networks and consortia Yes
Funding
Funding status Mixed
Details Ministère de la Recherche, Inserm, Conseil Scientifique de Radioprotection de EDF, MGEN, Fondation de France, Ligue Nationale contre le Cancer, Aviesan/ITMO, CEST de l'Institut Curie
Governance of the database
Sponsor(s) or organisation(s) responsible Institut National de la Santé et de la Recherche Médicale
Organisation status Public
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Cohort study
Database recruitment is carried out by an intermediary A selection of health institutions and services
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. Prospective Other bodies active in creating this cohort: Institut Curie, INSERM Inclusion cut-off date: 01/01/2014
Database objective
Main objective The objectives of the cohort involving women related to a child suffering from ataxia telangiectasia (AT) are multi-layered: 1. To monitor female relatives for early detection of breast cancer (BC). 2. To estimate the risk of cancer associated with AT genes with a focus on BC risk. To investigate the role of potential modifying factors for this risk such as radiation, hormonal factors etc. 3. To investigate the natural history of BC in AT heterozygous women
Inclusion criteria Breast cancer free women, of legal age and related to a child with ataxia telangiectasia-: mothers, sisters, aunts, grandmothers, maternal and paternal cousins. Recruited from families who participated in the first previous retrospective study by the team and new families contacted through treating physicians (paediatricians, neuro-paediatricians ...), geneticists, the AT research association (APRAT), Orphanet (information server on rare diseases and orphan drugs) and CEREDIH (reference centre for hereditary immunodeficiencies).
Population type
Age Adulthood (19 to 24 years)
Adulthood (25 to 44 years)
Adulthood (45 to 64 years)
Population covered General population
Gender Woman
Geography area International
Detail of the geography area International multicentric cohort (31 centres): Belgium, Luxembourg, France
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 01/2003
Date of last collection (YYYY or MM/YYYY) 2024
Size of the database
Size of the database (number of individuals) < 500 individuals
Details of the number of individuals 391 (2013)
Data
Database activity Current data collection
Type of data collected Clinical data
Declarative data
Paraclinical data
Biological data
Clinical data (detail) Direct physical measures
Medical registration
Declarative data (detail) Paper self-questionnaire
Paraclinical data (detail) Imaging
Biological data (detail) Type of samples taken: blood, tumour tissues
Presence of a biobank Yes
Contents of biobank Plasma
Tissues
Cell lines
DNA
DNAc/RNAm
Details of biobank content Plasma bank, DNA bank, RNA of lymphoblasts, DMSO frozen cells, cell lines, tumour tissue sample (breast cancer)
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method Self-administered questionnaire: from paper questionnaire Interview: from paper questionnaire
Participant monitoring Yes
Details on monitoring of participants Follow-up duration: 10 years
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://www.hal.inserm.fr/COFAT/
Description List of publications in HAL
Access
Terms of data access (charter for data provision, format of data, availability delay) Data may be used by academic teams Data may not be used by industrial teams
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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