Cancer Childhood, Development Delay, Predisposition, Genetic
Conditions
Brief summary
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.
Detailed description
-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.
Interventions
OTHERCollection of blood sample or saliva
at Inclusion
OTHERCollection of a tumor sample taken before the participation of the patient in study
at Inclusion
OTHERCollection of blood sample if tumor sample is not available
at Inclusion
Sponsors
University Hospital, Angers
Study design
Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
prospective multicenter study, not therapeutic,
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* For Patient cancer : * Child having developed a cancer combined with a delay of development and\\or an intellectual deficiency before the age of 18 years and followed for a cancer of the child in one of hospital center of the Société Française de lutte contre les Cancers et les leucémies de l'Enfant et de l'adolescent (SFCE) * At least a parent still alive and available to make genetic analyses * For Parent of cancer patient : * Parent whose child meets the criteria of inclusion of Cancer patient
Exclusion criteria
* For Cancer patient : * Genetic predisposition already identified at the child * Absence of histological confirmation * Child died without DNA of the available germinal lineage * For Parent of cancer patient : * Parent whose child doesn't meets the criteria of inclusion of Cancer patient
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number and type of germline and somatic genetic variants of pathological significance and associated with the disease. | At inclusion | 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. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Related to secondary objectives (1) : Identification of biological pathways involved in childhood cancer predisposition. | At inclusion | 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. |
| Related to secondary objectives (2) : Overall success rate. | At inclusion | 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. |
| Related to secondary objectives (3) : Number of clinical criteria justifying a WES. | At inclusion | 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. |
Countries
France, Reunion
Outcome results
None listed