The main objective is to study the genomic, transcriptomic, proteomic epigenomic, metabolomic and immune mechanisms of blasts and microenvironment cells associated with IT resistance through the constitution of a collection associating blood or marrow samples from patients with LA, MDS and MPS marrow samples from patients with LA, MDS and MPS at diagnosis, during treatment and at relapse and relapse and clinical annotations.
It is a collection of blood, marrow and oral epithelial cell samples taken longitudinally and oral epithelial cells taken longitudinally for each patient included, with each patient included, with the corresponding clinical data. An oral epithelial cell sample will be collected at inclusion from 2 swabs, which will allow extraction of DNA from healthy from healthy cells. During blood sampling necessary for care, an additional 40 ml of blood will be collected of 40 ml of blood will be collected in 10 tubes of 4 ml: 4 EDTA tubes, 4 heparinized heparinized tubes and 2 dry tubes. These additional collections will take place at the following times: * At inclusion * 7 days (+/- 2 days) after initiation of treatment * 14 days (+/- 2 days) after initiation of therapy * 21-42 days after initiation of therapy (early response assessment) * In case of complete remission * In case of relapse or progression During bone marrow punctures required for treatment, 6 ml of bone marrow bone marrow will be collected in 2 tubes of 3 ml: 1 EDTA tube and 1 heparinized tube. heparinized tube. These additional collections will take place at the following times following times: * At inclusion * 21-42 days after initiation of treatment (assessment of early response) early response) * In case of complete remission * In case of relapse or progression Patients will be followed for up to 2 years after inclusion.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
400
blood sampling, bone marrow aspirate and buccal swab
Acute leukemia/ Myeloproliferative/ myelodysplastic syndrome cells profiling (molecular analysis, epigenetic profile, drug sensitivity profile,immunophenotyping)
establishment of genomic and proteomic signatures as well as transcriptomic and metabolic profiles associated with IT resistance.
Time frame: up to 7 years
to study the resistance to treatments
study of the sensitivity to IT in vitro of primary cells from patients
Time frame: up to 7 years
Creation of murine cell models (Patient-derived xenografts, PDX) from patient blasts to study in vivo in order to study in vivo the mechanisms of resistance to treatment.
Establishment of xenografts in immunocompromised mice from primary cells of TI-resistant patients patients resistant to IT
Time frame: up to 7 years
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