NCT05602168

Collection of Sequential Samples From Patients With Malignant Myeloid Hemopathy for the Study of Treatment Resistance

Collection of Sequential Samples From Patients With Malignant Myeloid Hemopathy for the Study of Treatment Resistance: HEMATOBIO.02-IPC 2021-061

• Status: Not Yet Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 400 (estimated)
• Sponsor: Institut Paoli-Calmettes · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

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.

Detailed description

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.

Conditions

• Hematologic Cancer

Interventions

Type	Name	Description
OTHER	experimental:Acute leukemia/myelodysplastic or myeloproliferative disease	blood sampling, bone marrow aspirate and buccal swab

Timeline

• Start date: 2023-01-01
• Primary completion: 2030-01-01
• Completion: 2030-01-01
• First posted: 2022-11-01
• Last updated: 2022-11-01