Analysis of the individual radiosensitivity in pediatric oncology
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SCREENING
Masking
NONE
Enrollment
100
Blood sample collection : 2 X 5 ml
Centre François Baclesse
Caen, France
RECRUITINGCentre Oscar Lambret
Lille, France
NOT_YET_RECRUITINGProspectively validate the discriminating capacities of the RadioDtect© individual radiosensitivity blood test on the occurrence of early radio-induced toxicities.
The validation will be based on ATM protein quantification assay to predict acute toxicities
Time frame: 24 months
Prospectively validate the discriminating capacities of the RadioDtect© individual radiosensitivity blood test on the occurrence of early radio-induced toxicities.
evaluation of acute toxicities of grade ≥ 2 to 3 months according to NCI-CTCAE v4.03 criteria
Time frame: 24 months
Prospectively validate the discriminating capacities of the RadioDtect individual radiosensitivity blood test protein assay according on the occurrence of late radiation-induced toxicity at 12 months
The validation will be based on ATM protein quantification assay to predict late toxicities
Time frame: 12 months
Prospectively validate the discriminating capacities of the RadioDtect individual radiosensitivity blood test protein assay according on the occurrence of late radiation-induced toxicity at 12 months
evaluation of late toxicities of grade ≥ 2, according to NCI-CTCAE v4.03 criteria
Time frame: 12 months
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