Methodology: Prospective, multicentric, open, non-randomised, non-therapeutic, interventional study
To identify and characterise: * meaningful molecular genetic alterations, * meaningful immunological features of high risk childhood, adolescents and young adult cancers, at diagnosis, during patient treatment and follow-up (time dimension).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
600
biological sampling during treatment and follow-up
Number of patients with meaningful molecular genetic alterations
Identification of molecular genetic alterations based on molecular characterisation of tumor at diagnosis, during patient treatment and follow-up (time dimension)
Time frame: At the end of study (6 years)
Number of patients with meaningful immunological features
Identification and characterisation of the tumor microenvironment and the host's immunological profile, at diagnosis and during patient treatment
Time frame: At the end of study (6 years)
Number of patients with identification of new tumor-specific genetic characteristics during follow-up (clonal evolution)
Comparison between genetic variations identified at diagnosis and those identified on circulating tumor DNA during treatment, FU and/or relapse
Time frame: up to 6 years
Correlation between disease recurrence and molecular and/or immunological biomarkers
To characterise biomarkers, based on molecular analyses of tumour samples from diagnosis, for prognostic and predictive purposes. To characterise the tumour microenvironment and the host's immunological profile, for prognostic and predictive purposes. To identify potential prognostic and predictive biomarkers on samples collected during patient's treatment and follow-up, based on changes on circulating tumour DNA (ctDNA), detected by molecular biology techniques, and on immunological findings
Time frame: up to 6 years
Correlation between genetic variations and immune parameters
To compare molecular and immunological findings at diagnosis and during treatment (data integration)
Time frame: up to 6 years
Correlation between disease staging and immunological features
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Chu D'Amiens Picardie
Amiens, France
CHU Angers
Angers, France
CHRU de Besançon - Hôpital Jean-Minjoz
Besançon, France
CHU de Bordeaux - Hôpital des enfants - Groupe Hospitalier Pellegrin
Bordeaux, France
CHRU de Brest
Brest, France
CHU CAEN
Caen, France
Centre Régional de Cancérologie et Thrapie Cellulaire Pdiatrique (CRCTCP)
Clermont-Ferrand, France
CHU Hôpital d'Enfants
Dijon, France
CHU GRENOBLE Alpes - Hôpital Couple-Enfant
Grenoble, France
Centre Oscar Lambret
Lille, France
...and 20 more locations
To investigate the impact of the tumour microenvironment and host's immunological profile on the disease staging at diagnosis, by comparing patients with metastatic to patients with localised disease
Time frame: up to 6 years