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General Cancer Registry of French Polynesia

France, 1985
Reference ID
FRESH-PEF9392-en
Producer(s)
Florent De Vathaire
Metadata
DDI/XML JSON
Created on
Nov 15, 2025
Last modified
Nov 15, 2025
Page views
5
  • Identification
  • Scope
  • Coverage
  • Producers and sponsors
  • Study authorization
  • Sampling
  • Survey instrument
  • Data collection
  • Study activities
  • Quality standards
  • Data Access
  • Contacts
  • Metadata production

    • Identification

    Survey ID number

    FRESH-PEF9392-en
    Title

    General Cancer Registry of French Polynesia
    Country
    Name
    France
    Abstract

    To identify all new cancer cases among individuals living in French Polynesia. To conduct descriptive, analytic and evaluative epidemiological work with this data. Assessment of healthcare and diagnostic practices. Assessment of screening practices. Participation in etiological and prognostic research.
    Kind of Data

    ['Clinical data']
    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary URI
    Oncology health theme
    cim-11 http://id.who.int/icd/entity/564605304
    Environmental determinants: Other health determinant
    Environmental determinants health determinant
    Keywords
    Polynesia incidence diagnosis screening

    Coverage

    Universe

    {
    "level_sex_clusion_I": [
    "Male",
    "Female"
    ],
    "level_age_clusion_I": [
    "Infant (28 days to 2 years)",
    "Child, Preschool (2 to 5 years)",
    "Child (6 to 12 years)",
    "Young Adult (19 to 24 years)",
    "Adult (25 to 44 years)",
    "Middle Aged (45 to 64 years)",
    "Aged (65 to 79 years)",
    "Aged, 80 and over (80 years and more)"
    ],
    "level_type_clusion_I": [
    "Patients population"
    ],
    "level_type_clusion_other": "",
    "clusion_I": "",
    "clusion_E": ""
    }

    Producers and sponsors

    Primary investigators
    Name
    Florent De Vathaire
    Producers
    Name Role
    AUTORITE DE SURETE NUCLEAIRE ET DE RADIOPROTECTION (ASNR) sponsor
    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) sponsor

    Study authorization

    Agency
    Agency name
    CNIL

    Sampling

    Sampling Procedure

    ['Other']

    Survey instrument

    Questionnaires

    Access on specific project only
    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start
    1985
    Time Method

    Morbidity registry
    Mode of data collection
    • Converting or copying information into a structured record

    Study activities

    Study activities
    Type
    primary evaluation
    Description
    Health event/morbidity Health event/mortality

    Quality standards

    Other quality statement
    • Internal quality control for data validation by establishing quality indicators once a year. - Using quality criteria from the FRANCIM network and French National Committee of Registries. - Data validation protocol: comprehensive consultation of data sources from laboratories and DIMs (Medical Information Departments); missing and duplicated data control, inconsistency control performed using IARC Tools and corrections carried out.

    Data Access

    Access conditions

    Data can only be disseminated through direct involvement with those in charge of the registries.
    Availability Status

    Restricted access

    Contacts

    Contacts
    Name Email
    Florent De Vathaire florent.devathaire@gustaveroussy.fr

    Metadata production

    DDI Document ID

    FRESH-PEF9392-en
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