- Digestive cancers registry of Burgundy

Head :
Bouvier Anne-Marie, Centre de Recherche INSERM U866

Last update : 04/12/2012 | Version : 1 | ID : 217

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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 Digestive cancers registry of Burgundy
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 998024
General Aspects
Medical area Cancer research
Health determinants Geography
Others (details) digestive cancers
Keywords care practice, trends, digestive cancers, epidemiology, public health, survival
Scientific investigator(s) (Contact)
Name of the director Bouvier
Surname Anne-Marie
Address Registre des Cancers, Faculté de Médecine, BP 87900, 21079 Dijon Cedex
Phone + 33 (0)3 80 39 33 38
Email anne-marie.bouvier@u-bourgogne.fr
Unit Centre de Recherche INSERM U866
Organization CHU
Collaborations
Funding
Funding status Public
Details The National Public Health Institute (InVS) and the National Cancer Institute (INCa)
Governance of the database
Sponsor(s) or organisation(s) responsible University Hospital Dijon
Organisation status Public
Sponsor(s) or organisation(s) responsible University of Burgundy
Organisation status Public
Additional contact
Main features
Type of database
Type of database Morbidity registers
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. Selection of subjects having the required inclusion criteria.
Several sources are used to identify cases:
- Pathological cytology and anatomy laboratories
- Private or public physicians
- Screening organization structures
- Death certificates
- The ALD 30 file (concerning the list of 30 chronic diseases eligible for full cover)
- files from the PMSIs (French diagnosis-related group databases) of the départements' healthcare institutions.
- medical records
Database objective
Main objective Objectives of the registry in terms of public health (surveillance, evaluation):
1) determine the main health indicators: Incidence, Prevalence, Survival and their change over
time.
2) evaluate medical practices, paying particular attention to elderly subjects, and the trends concerning
healthcare quality indicators.
- Objectives of the registry in terms of research:
1) determination of at-risk groups and epidemiology of pre-cancerous lesions
2) study of quality of life at population level
3) development of new methodological approaches for survival analysis
4) biological epidemiology through the creation of a population-based tumor bank based to evaluate molecular prognostic markers
5) development of new immunological tests looking for colorectal screening,
protein signature
6) medico-economic analysis: cost of colorectal cancer, cost-effectiveness analysis of
screening strategies.
Inclusion criteria Malignant and invasive primary digestive tumors and
Malignant non-invasive tumors, called in situ or intra-epithelial, when no
invasive tumor of the same histological type or location has previously appeared in the
same subject. Incidence calculations only take account of invasive malignant tumors.
Population type
Age Newborns (birth to 28 days)
Infant (28 days to 2 years)
Early childhood (2 to 5 years)
Childhood (6 to 13 years)
Adolescence (13 to 18 years)
Adulthood (19 to 24 years)
Adulthood (25 to 44 years)
Adulthood (45 to 64 years)
Elderly (65 to 79 years)
Great age (80 years and more)
Population covered General population
Gender Male
Woman
Geography area Departmental
French regions covered by the database Bourgogne Franche-Comté
Detail of the geography area Burgundy region: Côte d'Or and Saône-et-Loire administrative areas ('departements')
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1976
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 1976- 2008: 37 500 cas/cases
Data
Database activity Current data collection
Type of data collected Clinical data
Paraclinical data
Biological data
Administrative data
Clinical data (detail) Direct physical measures
Paraclinical data (detail) diagnostic assessment, patterns of care
Biological data (detail) methodological coordination of a tumor bank gathering tissue samples of colorectal adenocarcinoma resections in the Côte d'Or département
Administrative data (detail) Identification data
Presence of a biobank Yes
Contents of biobank Tissues
Details of biobank content for resected colorectal cancers
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method active: the registry itself seeks out information from different sources.
Classifications used international nomenclatures
Participant monitoring Yes
Details on monitoring of participants Vital status - Active follow-up of colorectal cancers is carried out systematically in search of a progressive recurrence (locoregional recurrence or distant metastasis) or second cancer is recorded. Given that over 80% of these recurring cancers arise in the first three years, follow-up is conducted individually every n+3 years after diagnosis, and n+5 years for resection patients for curative purposes.
Links to administrative sources Yes
Linked administrative sources (detail) RNIPP
Promotion and access
Promotion
Link to the document http://www.ncbi.nlm.nih.gov/pubmed?term
Access
Terms of data access (charter for data provision, format of data, availability delay) exploitation and dissemination of data by scientific publications and oral communication
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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