Symptoms and General Pathology

All Conditions

Disease Susceptibility

Genetic Predisposition to Disease

Disease Attributes

* Collection of blood sample or saliva
* Collection of a tumor sample taken before the participation of the patient in study
* Collection of blood sample if tumor sample is not available

Collection of blood sample or saliva

Collection of a tumor sample taken before the participation of the patient in study

Collection of blood sample if tumor sample is not available

Elsa BERARDI

Catherine DEVOLDERE, MD

Isabelle PELLIER, PU-PH

Virginie BUBIEN, MD

Julie TINAT, MD

Liana-Stefania CARAUSU, MD

Christine FRANCANNET, MD

Laurence OLIVIER-FAIVRE, PU-PH

Dominique PLANTAZ, PU-PH

Sophie LEJEUNE, MD

Christophe PIGUET, MD

Nadege CORRADINI, MD

Delphine SIGAUDY, MD

Carole COZE, MD

Stéphanie HAOUY, MD

Bruno LEHEUP, MD

Bertrand ISIDOR, MD

Marilyne DUPUY, MD

Franck BOURDEAUT, MD

Hélène MARTELLI, PU-PH

Sabine SARNACKI, PU-PH

Vincent COULOIGNER, PU-PH

Hélène BOUTROUX, MD

Philippe DENIZEAU, MD

Pascale SCHNEIDER, PU-PH

Jean-Louis STEPHAN, MD

Catherine PAILLARD, PU-PH

Marion GILLIBERT-YVERT, MD

Léa GUERRINI-ROUSSEAU, MD

Yves REGUERRE, MD

Isabelle PELLIER, Pr

Other than high-dose radiation and previous chemotherapy, few strong risk factors have been identified as causes of childhood cancer. Geneticists estimate that 5 to 10% of all cancers diagnosed during the paediatric period occur in children born with a genetic mutation, increasing their lifetime risk of neoplasia. Such genetic risk is higher in children with congenital anomalies and specific genetic syndromes. Some germline genetic alterations are well known (e.g. P53 protein (P53), Neurofibromatosis type 1(NF1)), however many children with none of these mutations have clinical presentations that strongly suggest the involvement of a genetic predisposition. Comprehensive genetic testing for all such patients is an important factor for improving disease surveillance. Such opportunities are now available thanks to whole exome sequencing (WES). In oncology, an important clinical application of WES will be to routinely identify mutations associated with inherited cancer predispositions and to guide cancer risk-management decisions.

Our project is a national translational multicenter genetics study aimed at identifying genes involved in paediatric cancer predisposition by WES in a very select population of children with both developmental delay and cancer. Our project relies on the TED register (Tumeur Et Développement), an initiative by the French organisation SFCE (Société Française de lutte contre les Cancers et les leucémies de l'Enfant et de l'Adolescent) involving 30 child cancer units in France. This database includes the information of more than 500 paediatric cancer patients with congenital abnormalities. The investigators plan to sequence the germline and tumour exome of 100 patients with developmental delay in a trio-design consisting of 300 people and 100 tumours.

The investigators believe that the ExoCaRe project will provide answers to the genetic origins of certain particular childhood cancers. The ExoCaRe project relies on a genetic study to identify genetic risk factors for rare forms of childhood cancer and aims to establish more personalised treatment. It is aimed at improving genetic counselling for families and will be fully integrated in the genetic counselling process. The information provided by our study will be used to improve the management approach to an initial cancer by clarifying the risks of other cancers in related families. The investigators hope to identify new germline genes predisposing to cancer that will be of interest in understanding tumour biology.

-Primary objective : Our aim is to identify new mutations and genes involved in paediatric cancer predisposition associating developmental delay by WES of a sub-cohort of patients included in the TED database.

-Secondary objectives :

1. Describe inherited predisposition to cancer.
2. Improve genetic counselling processes.
3. Initiate clinical exome sequencing in childhood cancer treatment.

prospective multicenter study, not therapeutic,

EXOme Rare Cancers in Children (EXOCARE)

An Investigation of Susceptibility Genes for Rare Cancers in Children by Exome Sequencing

WES and RNA sequence data will be used to identify and characterise germline and somatic genetic variants of pathological significance and associated with the disease.

Descriptive statistics, such as counts and proportions of variants of pathological significance risk will be computed within each patient and family.

The deleterious mutations that the investigators will identify in genes related to childhood cancer predisposition will help to have a comprehensive framework of biological pathways involved in childhood cancer predisposition.

Success is defined by the combined successes of quality interpretable genomic data are generated from sequencing tumor and germline tissues, and communicating genomic test results to the primary oncologist and the patient and his/her parents.

Descriptive statistics, such as counts and proportions of success by clinical presentation of the disease, by cancer types, by features of developmental delay, and, by class of age.

University Hospital, Angers

Spots Global Cancer Trial Database for development delay