- Hérault Cancer Registry (Certified Registry 2010-2013)

Head :
Trétarre Brigitte

Last update : 07/08/2015 | Version : 2 | ID : 223

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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 Hérault Cancer Registry (Certified Registry 2010-2013)
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 997109
General Aspects
Medical area Cancer research
Health determinants Geography
Keywords population registry, survival, incidence, mortality
Scientific investigator(s) (Contact)
Name of the director Trétarre
Surname Brigitte
Address Registre des tumeurs de l’Hérault- 208 rue des Apothicaires- 34298 Montpellier Cedex 5
Phone + 33 (0)4 67 41 34 17
Email registre-tumeur@wanadoo.fr
Collaborations
Funding
Funding status Public
Details InVS and INCA.
Governance of the database
Sponsor(s) or organisation(s) responsible Centre de Lutte Contre le Cancer Val d’Aurelle
Organisation status Both
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Selection of subjects fulfilling the required inclusion criteria. Several sources are used to identify cases:- anatomopathology laboratories- private radiotherapy practices- haematology laboratory - regional oncology network (ONCO-LR)- organised mass screening facilities for breast cancer and colon cancer (34 Screening and IMIM)- European Randomised Study of Screening for Prostate Cancer (ERSPC) - PMSI data - health insurance funds - clinical departments (3 private and 3 public) - national brain tumour registration - multidisciplinary urology meetings - Toulouse Cancer Prevention Centre (CLCC) - Castres Hospital- Nîmes University Hospital Centre (UHC) - Gustave Roussy Institute.
Database objective
Main objective Objectives of the registry in terms of public health (surveillance, assessment):
The tumour registry is the only facility that can assess all of the actions taken over the last 20 years within the département in the field of prevention and screening (breast cancer, prostate cancer, colon-rectum cancer).
The registry monitors incidence and survival for all cancers over time according to all prognostic factors, and provides information on all interval cancers occurring after a negative screening examination.
- Objectives of the registry in terms of research:
The registry is conducting a number of studies (alone or together with other French or European registry networks) to address the need for epidemiological knowledge:
- Descriptive epidemiology: all data concerning cancer in the Hérault département is published and distributed at regular intervals to the whole medical community every two years i.e., incidence and mortality data.
- Analytical epidemiology: relative survival, prevalence, cohort and case-control studies, interval cancers.
- Prognostic factor studies: medico-economic studies, studies on therapies and healthcare channels.
Data from the registry is used by the FRANCIM network in France and by the EUROCARE group at European level to estimate national and regional cancer incidence and prevalence in France, as well as survival analysis.
Inclusion criteria All new invasive tumours, as well as in situ breast, cervix, colorectal and bladder tumours, skin melanomas, bladder pTa and benign tumours of the central nervous system that are diagnosed in individuals living in Hérault, regardless of where they are treated. Only basocellular skin carcinoma are excluded from the registry. Contralateral breast tumours in the same patient are recorded but not counted in incidents, and are not sent to the FRANCIM common database, in accordance with the rules defined by the European Network Cancer Registry (ENCR) and FRANCIM (French cancer registry network certified by the National Registries Committee).
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 Languedoc-Roussillon Midi-Pyrénées
Detail of the geography area Hérault
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1985
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 1987-2008: 96,535 patients, 104,252 cases (95,136 invasive).
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) Paraclinical examinations for determining tumour stage.
Biological data (detail) Tumour histology, grade, 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 or passive collection: - computerised files - computerised listing - paper factsheets - paper listing.
Participant monitoring Yes
Details on monitoring of participants Survival.
Links to administrative sources Yes
Linked administrative sources (detail) Cépi DC, RNIPP.
Promotion and access
Promotion
Link to the document http://www.registre-tumeurs-herault.fr/
Link to the document http://tinyurl.com/PUBMED-RTH
Description Liste des publications dans Pubmed
Link to the document http://tinyurl.com/HAL-RTH
Description Liste des publications dans HAL
Access
Terms of data access (charter for data provision, format of data, availability delay) Website: downloadable data.
Access to aggregated data Free access
Access to individual data Access on specific project only

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