- Finistère Registry for Digestive Tumours (Certified Registry 2013-2016)

Head :
Robaszkiewicz Michel, Directeur administratif
Nousbaum Jean-Baptiste, Directeur scientifique
Cariou-Daoulas Mélanie, Coordinatrice

Last update : 10/02/2015 | Version : 2 | ID : 228

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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 Finistère Registry for Digestive Tumours (Certified Registry 2013-2016)
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 908270
General Aspects
Medical area Cancer research
Gastroenterology et hepatology
Scientific investigator(s) (Contact)
Name of the director Robaszkiewicz
Surname Michel
Address Registre Finistérien des tumeurs digestives, CHUR MORVAN, Bât 1, 6 avenue Foch, 29609 Brest Cedex
Phone +33 (0)2 98 34 71 54
Email michel.robaszkiewicz@chu-brest.fr
Unit Directeur administratif
Organization CHUR
Name of the director Nousbaum
Surname Jean-Baptiste
Address Registre Finistérien des tumeurs digestives, CHUR MORVAN, Bât 1, 6 avenue Foch, 29609 Brest Cedex
Phone + 33 (0)2 98 34 71 48
Email jean-baptiste.nousbaum@chu-brest.fr
Unit Directeur scientifique
Organization CHUR
Name of the director Cariou-Daoulas
Surname Mélanie
Address Registre Finistérien des tumeurs digestives, CHUR MORVAN, Bât 1, 6 avenue Foch, 29609 Brest Cedex
Phone + 33 (0)2 29 02 01 52
Email registre-du-finistere@laposte.net
Unit Coordinatrice
Organization CHUR
Collaborations
Funding
Funding status Public
Details French Institute for Public Health Surveillance - INVS National Cancer Institute - InCA League
Governance of the database
Sponsor(s) or organisation(s) responsible CHU Brest
Organisation status Public
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Selection of subjects meeting the inclusion criteria. Several sources are used to identify cases:- Clinical departments - University Hospital Centres (UHC)- Other public clinical departments- Private clinical departments- Private gastroenterologist practices – General practitioner surgeries - Medical Information Department (DIM) of the UHC - DIM of other institutions - Anatomopathology laboratory - Regional oncology networks – Civil registry - National PMSI database - Local medical departments of various health insurance funds (CPAM in Finistère, MSA, RSI, etc.).
Database objective
Main objective Objectives of the registry in terms of public health (surveillance, evaluation):
Thanks to the multi-source collection of digestive cancer cases, the registry's aim is to produce
quality data for calculating health indicators: it allows for the exact measurement of
incidence trends for digestive cancers depending on the tumour site or
anatomopathological type as well as patient survival.
By recording incident cancer cases, in the years to come, we will be able to evaluate the efficacy of Hémoccult screening for colorectal cancer, conducted in the département since June 2004 (Cancer Screening Association ADEC 29).

- Objectives of the registry in terms of research:
The digestive tumour registry has already been used for medical theses and
publications. Locally, incidence and survival studies are undertaken on a regular basis by the
registry's team. We also have projects with local partners: the Brest University Hospital Centre team,
University of West Brittany (prognostic factor of statin prescription on the occurrence of cancers).

The registry's data covers the entire validated period (1984-2006) and is sent annually to the national cancer incidence base managed by the FRANCIM network, the French Institute for Public Health Surveillance and Lyon Civil Hospices. As such, we are participating in the national cancer surveillance programme and contributing to national research.
Inclusion criteria The registry identifies all patients affected with a primitive malignant tumour, including in situ cancer of the digestive tract, liver, pancreas, biliary tracts, peritoneum and retroperitoneal tissue.
The date of incidence must fall after 01 January 1984.
Patients must live in Finistère and consent to the registration of their cases.
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 Sick population
Gender Male
Woman
Geography area Departmental
French regions covered by the database Bretagne
Detail of the geography area Finistère and bordering départements.
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1984
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 1984-2010: 27371 reported 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) Medical imaging.
Biological data (detail) Tumour markers.
Administrative data (detail) Identification data.
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method Active, the registry shall research information from different sources.
Classifications used ICD-O'3
Participant monitoring Yes
Details on monitoring of participants - Systematic for invasive malignant tumour and in situ carcinoma cases - vital status.
Links to administrative sources Yes
Linked administrative sources (detail) RNIPP.
Promotion and access
Promotion
Link to the document http://tinyurl.com/PUBMED-RFTD
Description Liste des publications dans Pubmed
Access
Terms of data access (charter for data provision, format of data, availability delay) Data promotion and distribution through 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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