RNTSE - French National Registry of Childhood Solid Tumors (certified registry)
Responsable(s) :
Lacour Brigitte, Registre National des Tumeurs Solides de l'Enfant
Date de modification : 02/07/2015 | Version : 2 | ID : 64
| Général | |
| Identification | |
| Nom détaillé | French National Registry of Childhood Solid Tumors (certified registry) |
| Sigle ou acronyme | RNTSE |
| Numéro d'enregistrement (ID-RCB ou EUDRACT, CNIL, CPP, etc.) | 900183 |
| Thématiques générales | |
| Domaine médical |
Cancer research |
| Déterminants de santé |
Geography |
| Mots-clés | childadolescent |
| Responsable(s) scientifique(s) | |
| Nom du responsable | Lacour |
| Prénom | Brigitte |
| Adresse | Faculté de Médecine, 9 rue de la Forêt de la Haye, 54500 Vandoeuvre les Nancy |
| Téléphone | 0383683861 |
| brigitte.lacour@medecine.uhp-nancy.fr | |
| Laboratoire | Registre National des Tumeurs Solides de l'Enfant |
| Organisme | CHU |
| Collaborations | |
| Financements | |
| Financements |
Public |
| Précisions | - Institut national de veille sanitaire (InVS)- Institut national du cancer (INCa) |
| Gouvernance de la base de données | |
| Organisation(s) responsable(s) ou promoteur | CHU Nancy |
| Statut de l’organisation |
Secteur Public |
| Organisation(s) responsable(s) ou promoteur | ARECEA (Association pour la Recherche en Epidémiologie des Cancers de l'Enfant et de l'Adolescent) |
| Statut de l’organisation |
Secteur Privé |
| Contact(s) supplémentaire(s) | |
| Caractéristiques | |
| Type de base de données | |
| Type de base de données |
Morbidity registers |
| Informations complémentaires concernant la constitution de l'échantillon | Selection of subjects having the required inclusion criteria. |
| Objectif de la base de données | |
| Objectif principal |
Objectives in terms of public health (surveillance, evaluation):
1) Produce national reference rates on the incidence of solid tumors in children and on their histological distribution and monitor the geographical and temporal variations of this. 2) Provide the survival rates for the various cancers in the general population, all treatments taken as a whole and monitor the geographical and temporal variations in this. 3) Describe the care sectors followed by children, from the first symptoms to the treatment, and the methods for care as well as its determinants. Collaborate with clinicians of the French Society for the fight against Cancers in Childhood and Adolescent Cancers (SFCE) on the setting up of long-term follow-up of cohorts of children with cancer. Objectives in terms of research: Conduct and associate ecological studies and case/control studies concerning the risks of cancer associated with environmental exposure, population movements, the way of life and early conditions of exposure to common infections, genetic factors interacting or not interacting with the environmental factors (the etiologic research work is particularly developed by UMRS-1018 Team 6 of Inserm). |
| Critères d'inclusion |
The following are included:
All solid tumors in children defined in the International Classification of Childhood Cancers (ICCC) and belonging to the diagnostic groups III to XII, as well as the ""borderline"" tumors and certain benign tumors. Appearing starting on January 1, 2000 in a child under the age of 15 years on the date of the first sure diagnostic, and for whom the usual domicile is located in metropolitan France. Starting on January 1, 2011, extension of the recording up to the age of 18 years for all the cases domiciled in metropolitan France and in an Overseas Département (Guadeloupe, French Guiana, Martinique, Reunion) |
| Type de population | |
| 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) |
| Population concernée |
Sick population |
| Sexe |
Male Woman |
| Champ géographique |
National |
| Détail du champ géographique | Metropolitan France (+ DOM since 01/01/2011) |
| Collecte | |
| Dates | |
| Année du premier recueil | 2000 |
| Taille de la base de données | |
| Taille de la base de données (en nombre d'individus) |
[1000-10 000[ individuals |
| Détail du nombre d'individus | 2003: 1045 cases 2004: 1031 cases 2005: 1012 cases2006: 1025 cases |
| Données | |
| Activité de la base |
Current data collection |
| Type de données recueillies |
Clinical data Administrative data |
| Données cliniques, précisions |
Direct physical measures |
| Données administratives, précisions | Identification data (Last name, First name, Maiden name of the mother, Date of birth, Commune of birth, Insee Code, Commune of residency for the diagnostic, Insee Code, Full address of the diagnostic, Sex) |
| Existence d’une biothèque |
No |
| Paramètres de santé étudiés |
Health event/morbidity Health care consumption and services |
| Consommation de soins, précisions |
Hospitalization Medical/paramedical consultation Medicines consumption |
| Modalités | |
| Mode de recueil des données | Active collection in the hospital departments by survey takers |
| Nomenclatures employées | ICD-O 3 and grouped according to ICCC |
| Suivi des participants |
Yes |
| Détail du suivi | Vital status Project to collect the serious health events during follow-up by crossing the data with the data of the SNIIR-AM (not yet operational) |
| Appariement avec des sources administratives |
No |
| Valorisation et accès | |
| Valorisation et accès | |
| Lien vers le document | http://www.chu-nancy.fr/rntse/ |
| Lien vers le document | http://www.hal.inserm.fr/RNTSE |
| Description | List of publications in HAL |
| Lien vers le document | http://www.ncbi.nlm.nih.gov/pubmed/?term=NRCST[title%2Fabstract]+OR+%28%28NRCH[title%2Fabstract]+OR+Escale+OR+Estelle%29+AND+Clavel[author]%29+OR+geocap+OR+mobi-kids+OR+%22Childhood+Leukemia+International+Consortium%22 |
| Description | List of publications in Pubmed |
| Accès | |
| Charte d'accès aux données (convention de mise à disposition, format de données et délais de mise à disposition) |
Website: http://www.chu-nancy.fr/rntse/
Annual activity report intended for InVS and Inserm. Integration in the ""The cancer situation in France"" report published every year by INCa Publications in specialized reviews Communication at scientific congresses |
| Accès aux données agrégées |
Access on specific project only |
| Accès aux données individuelles |
Access on specific project only |
