- Limousin Region General Cancer Registry (CERTIFIED REGISTRY 2015-2020)

Head :
Leone Nathalie, Pôle Biologie Cancer

Last update : 03/07/2016 | Version : 2 | ID : 5405

print
Print
xml
XML

Export to XML

Please choose the format :

pdf
PDF
xml
CSV (Excel)

Export to CSV

What sections do you want to export ?

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
Select all | Invert selection | No selection

Which version do you want to export ?

send
Send
General
Identification
Detailed name Limousin Region General Cancer Registry (CERTIFIED REGISTRY 2015-2020)
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 999305
General Aspects
Medical area Cancer research
Health determinants Medicine
Keywords oncogeriatrics
Scientific investigator(s) (Contact)
Name of the director Leone
Surname Nathalie
Address Hôpital Le Cluzeau, 23 Avenue Dominique Larrey, 87042 Limoges Cedex
Phone + 33 (0)5 55 05 88 68
Email nathalie.leone@chu-limoges.fr
Unit Pôle Biologie Cancer
Organization CHU de Limoges
Collaborations
Funding
Funding status Public
Details French Institute for Public Health Surveillance (InVS), French National Cancer Institute (INCa) and the Limousin Regional Health Agency (ARS).
Governance of the database
Sponsor(s) or organisation(s) responsible CHU, Hôpital Le Cluzeau, Limoges
Organisation status Public
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Selection of subjects fulfilling required criteria. Several sources are used to identify cases: - Anatomic cytopathology laboratories - molecular, haematology and cytogenetic laboratories - medical information departments (PMSI) - health insurance services (ALD) - summaries from multidisciplinary meetings (RCP) - clinical services - treating physicians - private radiotherapy centres - childhood cancer registries.
Database objective
Main objective Registry objectives regarding public health (surveillance, assessment):
- To participate in epidemiological cancer surveillance locally (Haute-Vienne and Limousin region), nationally (French network of cancer registries, FRANCIM) and internationally (European Network of Cancer Registries (ENCR)) and the International Agency for Research on Cancer (IARC) by publishing data on incidence, prevalence and survival according to location, sex, age and year of diagnosis. The registry may also identify possible cancer clusters and contribute to studies on measuring population exposure to probable or possible carcinogens, as well as the existence and nature of the causal relationship. Both Limousin and Haute-Vienne are concerned by the presence of natural radioactivity (radon) and former uranium mining sites.
- To contribute to the assessment of primary and secondary preventative initiatives (organised cancer screening), patient treatment and healthcare requirements in the general population. As the second oldest European region (after Liguria), Limousin is an indication of the future of geriatric oncology in France.
Registry research objectives:
- To participate in the FRANCIM network in national survival studies and "high resolution" studies on cancer treatment.
- To identify specific demographic traits in the territory covered by the registry that may further expertise in geriatric oncology.
Inclusion criteria All cases of primary invasive tumours (haematological malignancies and solid tumours, except basocellular skin carcinoma), in situ tumours (breast, cervix, colorectal, bladder and urinary tract, melanoma), benign tumours or unpredictable developments in the central nervous system and the bladder, as well as borderline tumours in the ovaries occurring in patients living in Haute-Vienne at the time of diagnosis, regardless of treatment location.
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 Aquitaine Limousin Poitou-Charentes
Detail of the geography area Haute-Vienne, 375,914 inhabitants as of 01 January 2009, source: INSEE.
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 2003
Date of last collection (YYYY or MM/YYYY) 2008
Size of the database
Size of the database (number of individuals) [10 000-20 000[ individuals
Details of the number of individuals 2003-2008 : 14,381
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) All further examinations that provide information on tumour coding.
Biological data (detail) All further examinations that provide information on tumour coding.
Administrative data (detail) Identification data (surname, first name, date of birth, place of birth, address).
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method Active or passive collection (CNIL approval): - receipt of anatomic cytopathological and cytohaematological reports, lists of admissions (PMSI) and long-term diseases. Data transferred by encrypted digital files. - active search for additional information in medical files.
Classifications used CIM-O, TNM.
Participant monitoring Yes
Monitoring procedures Monitoring by contact with the referring doctor
Monitoring by crossing with a medical-administrative database
Details on monitoring of participants Vital status, death, date of latest developments. Active follow-up is carried out on the sample (FRANCIM "High Resolution" surveys). Passive follow-up is carried out on information received by the registry.
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/22123138
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/18449095
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/12108336
Link to the document http://www.ncbi.nlm.nih.gov/pubmed?term
Link to the document http://tinyurl.com/PUBMED-RGCRL
Link to the document Survie-des-personnes-atteintes-de-cancer-France-metropolitaine-1989-2013-tumeurs-solides_2016.pdf
Access
Terms of data access (charter for data provision, format of data, availability delay) Incidence data are available in aggregate format on the registry website, according to year, location, sex and age.
Haute-Vienne data is included in the common French network cancer registry database: data may be accessed through FRANCIM.
Data are published locally (in collaboration with the Limousin Health Monitoring Agency (ORS)), internationally (FRANCIM publications) and internationally (ENCR).
Access to aggregated data Free access
Access to individual data Access on specific project only

Partners - FAQ - Contact - Site map - Legal notices - Administration - Updated on December 15 2020 - Version 4.10.05

View Edit Create here