RCT - Tarn Cancer Registry (Certified Registry 2020-2025)

Head :
GROSCLAUDE Pascale, U1027 EPIDEMIOLOGIE ET ANALYSES EN SANTE PUBLIQUE : RISQUES, MALADIES CHRONIQUES ET HANDICAPS
Daubisse-Marliac Laetitia, U1027 EPIDEMIOLOGIE ET ANALYSES EN SANTE PUBLIQUE : RISQUES, MALADIES CHRONIQUES ET HANDICAPS

Last update : 09/10/2020 | Version : 2 | ID : 172

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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 Tarn Cancer Registry (Certified Registry 2020-2025)
Sign or acronym RCT
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 99 80 15 (12/1998), 99 80 15 Version 2 (10/2003)
General Aspects
Medical area Cancer research
Keywords Francim, cancer epidemiology
Scientific investigator(s) (Contact)
Name of the director GROSCLAUDE
Surname Pascale
Phone +33 (0)5 63 47 59 51
Email pascale.grosclaude@inserm.fr ; registre81@orange.fr
Unit U1027 EPIDEMIOLOGIE ET ANALYSES EN SANTE PUBLIQUE : RISQUES, MALADIES CHRONIQUES ET HANDICAPS
Organization INSERM - Institut National de la Santé et de la Recherche Médicale
Name of the director Daubisse-Marliac
Surname Laetitia
Address 11 rue Lavazière 81012 Albi cedex
Phone 05 63 47 59 51
Email laetitia.daubisse-marliac@inserm.fr
Unit U1027 EPIDEMIOLOGIE ET ANALYSES EN SANTE PUBLIQUE : RISQUES, MALADIES CHRONIQUES ET HANDICAPS
Organization INSERM - Institut National de la Santé et de la Recherche Médicale
Collaborations
Funding
Funding status Public
Details Inca, SPF, Tarn general council, French League against Cancer.
Governance of the database
Sponsor(s) or organisation(s) responsible Institut Claudius Regaud (Centre Régional de lutte contre le cancer)
Organisation status Public
Sponsor(s) or organisation(s) responsible Association recherche en épidémiologie et prévention
Organisation status Private
Additional contact
Main features
Type of database
Type of database Morbidity registers
Database objective
Main objective In the area of public health:
(1) To produce quality data to calculate health indicators for incidence, survival and prevalence.
(2) To participate in the French network of cancer registries (FRANCIM) and to collaborate with SPF and INCa as part of the national cancer surveillance programme.
(3) To work with local stakeholders at a regional level (ARS, Regional cancer network, screening sites) and to concentrate on the local use of the generated knowledge (SROS cancer research, assessment of requirements, initial and continuous training).
(4) To assess the impact of the disease on the population scale: prevalence, survival with or without the disease.

In the area of research:
(1) To learn about the distribution of therapeutic innovations throughout the population and its impact from a health and economic standpoint
(2) To assess the heterogeneity factors in the distribution of cancer treatment developments and their impact in terms of social health inequality in primary and secondary healthcare usage.
(3) To participate in studies initiated by others by providing them with local knowledge from the registry team and data collected in Tarn.
Inclusion criteria All cases of invasive malignant tumors (except basocellular skin carcinoma) + in situ breast, colorectal, cervical, urinary tract and borderline ovarian tumours.
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
Pathology C00-C97 - Malignant neoplasms
Gender Male
Woman
Geography area Departmental
French regions covered by the database Languedoc-Roussillon Midi-Pyrénées
Detail of the geography area Tarn
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1982
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 60,000
Data
Database activity Current data collection
Type of data collected Clinical data
Paraclinical data
Biological data
Administrative data
Clinical data (detail) Direct physical measures
Medical registration
Paraclinical data (detail) Diagnostic assessment, anatomopathological report.
Biological data (detail) Markers.
Administrative data (detail) Surname, first name, date and place of birth, address.
Presence of a biobank No
Health parameters studied Health event/morbidity
Health care consumption and services
Care consumption (detail) Hospitalization
Procedures
Data collection method Systematic collection of information to identify cases is carried out using: (1) ALD information sources (2) PMSI information sources (3) the regional cancer treatment network (4) anatomic pathology laboratories (6) clinical and hospital departments (7) radiotherapy centres (8) specialist practices and (9) electoral registers.
Classifications used CIM-O; TNM
Quality procedure(s) used FRANCIM procedure and ENCR rules
Participant monitoring Yes
Details on monitoring of participants Vital status.
Links to administrative sources Yes
Linked administrative sources (detail) PMSI, ALD, RNIPP
Promotion and access
Promotion
Link to the document http://www.ncbi.nlm.nih.gov/pubmed
Access
Dedicated website https://www.onco-occitanie.fr/pro/page/registre-des-cancers-du-tarn
Terms of data access (charter for data provision, format of data, availability delay) RCT website.
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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