- CALVADOS GENERAL CANCER REGISTRY (CERTIFIED REGISTRY 2013-2016)

Head :
Guizard Anne-Valérie, Registre Général des Tumeurs du Calvados et Enquête Permanente Cancer

Last update : 10/19/2015 | Version : 3 | ID : 1035

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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 CALVADOS GENERAL CANCER REGISTRY (CERTIFIED REGISTRY 2013-2016)
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 115.299
General Aspects
Medical area Cancer research
Scientific investigator(s) (Contact)
Name of the director Guizard
Surname Anne-Valérie
Address Centre François Baclesse, 3 av General Harris, BP 5026 14076 Caen Cedex 05
Phone 02 31 45 52 45
Email AV.GUIZARD@baclesse.fr
Unit Registre Général des Tumeurs du Calvados et Enquête Permanente Cancer
Organization Centre de Lutte Contre le Cancer François
Collaborations
Funding
Funding status Public
Details InVS, INCA and INSERM.
Governance of the database
Sponsor(s) or organisation(s) responsible Centre de Lutte Contre le Cancer François Baclesse
Organisation status Private
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Selection of subjects meeting the required inclusion criteria. Several sources used to identify cases:- Anatomopathology laboratories - Private clinics (medical information department/DIM)- General hospitals (DIM)- Cancer Prevention Centres- Private radiotherapy centres- University Hospital Centres (DIM)- Paediatric oncology department- Health Insurance Funds- Minutes from the Multidisciplinary Consultation Meeting.
Database objective
Main objective The main purpose of the registry is to produce, through active and exhaustive collection of cases, data enabling indicators to be calculated for monitoring population health (incidence, survival and prevalence). In this regard, the Registry takes part in the national cancer surveillance programme from the French Institute for Public Health Surveillance (InVS).
The Registry's data is included in the database of the French cancer registry network
(FRANCIM), which is managed by the Biostatistics Laboratory of the Lyon-Sud Faculty of Medicine in connection with the InVS. It is used to estimate cancer incidence across France as a whole and per region, and to study incidence trends over the last 25 years.
It is also used to estimate prevalence and analyse survival on a regular basis by the FRANCIM network for France and by the EUROCARE group for Europe.
The registry data is also sent at regular intervals to the International Agency for Research on Cancer (Lyon) for publication in Cancer Incidence in Five Continents from the first available five-year period.

The Registry takes part in cooperative studies conducted as part of the FRANCIM and EUROCARE networks aimed at evaluating medical practices in the population, providing recommendations at Consensus conferences and measuring their impact on public health. These studies focussed on the following sites: thyroid, breast, lung, prostate, testicle and skin melanoma.

Objectives of the registry in terms of research:
- Social inequalities and access to healthcare;
- Reintegration of patients in long-term remission or who have recovered from cancer;
- Pesticide exposure and cancer risk in the agricultural environment (EPI95 cohort).
Inclusion criteria New cases of invasive and in situ cancer as well as all brain tumours, regardless of behaviour (except digestive cancer).
Basocellular skin carcinoma have not been recorded since 1990;
Haematological diseases have not been recorded since 2001 (Lower Normandy Regional Registry
for Haematological Diseases creation date).
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 Normandie
Detail of the geography area Calvados
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1978
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 61,910 incident cases since beginning of registration.
Data
Database activity Current data collection
Type of data collected Clinical data
Administrative data
Clinical data (detail) Direct physical measures
Administrative data (detail) - Last name, first name - maiden name - date of birth - town (country) of birth- address- sex - profession at the time of diagnosis.
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method - Computer file - paper files- database consultation.
Participant monitoring Yes
Details on monitoring of participants Vital status.
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://tinyurl.com/PUBMED-CGCR
Description Liste des publications dans Pubmed
Access
Terms of data access (charter for data provision, format of data, availability delay) Incidence data is available in aggregate form according to cancer location, year, sex and age. It is published at regular intervals at local and national level, French Institute for Public Health Surveillance/InVS and IARC.
Access to aggregated data Free access
Access to individual data Access on specific project only

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