HomeFrench National Registry of Childhood Cancer (Registre National des Cancers de l’Enfant)
French National Registry of Childhood Cancer (Registre National des Cancers de l’Enfant) Profile Page
French National Registry of Childhood Cancer (Registre National des Cancers de l’Enfant)
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Faculté de Médecine
9 avenue de la Forêt de Haye
BP 184
VANDOEUVRE Cedex
54505
France (metropolitan)
Dr Jacqueline Clavel (Villejuif) and Dr. Brigitte Lacour (Nancy)

Description

The French National Registry of Childhood Cancer (RNCE) is composed of the French National Registry of Childhood Haematological Malignancies (RNHE), located in Paul Brousse hospital in Villejuif, and the French National Registry of Childhood Solid Tumours (RNTSE) hosted by the CHRU of Nancy.

RNCE is a national, population-based ancer registry for children. The registry collects precise data on each new cancer, or of borderline tumour, diagnosed among children and adolescents before their 18th birthday, residing in France. It provides a solid baseline for public health surveillance and to undertake cancer research.

The registry is co-directed by two chief scientific coordinators: Dr Jacqueline Clavel, chief scientific officer of the French National Registry of Childhood Haematological Malignancies (RNHE, INSERM) and Dr Brigitte Lacour, chief scientific officer of the French National Registry of Childhood Solid Tumours (RNTSE, CHRU Nancy).

The registry records all new cancer cases diagnosed in mainland France residents under age 15 years (since 1990 for haematological malignancies, since 2000 for solid tumours). Since the 1st January 2011, registration has been extended to include adolescents up to the age of 17 years, residing in mainland France or in overseas departments.

Registration includes data on diagnosis and treatment. RNCE monitors trends of remission rate, as well as the occurrence of potential late adverse events related to the disease or treatments.

It answers several goals of the French national Cancer plan.

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