Collection of Sequential Samples From Patients With Malignant Myeloid Hemopathy for the Study of Treatment Resistance
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: experimental:Acute leukemia/myelodysplastic or myeloproliferative disease.
- Who it may be relevant to
- Registry conditions: Hematologic Cancer. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Collection of Sequential Samples From Patients With Malignant Myeloid Hemopathy for the Study of Treatment Resistance: HEMATOBIO.02-IPC 2021-061
Overview
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.
Interventions
- Other experimental:Acute leukemia/myelodysplastic or myeloproliferative disease
blood sampling, bone marrow aspirate and buccal swab
Primary outcome measures
- Acute leukemia/ Myeloproliferative/ myelodysplastic syndrome cells profiling (molecular analysis, epigenetic profile, drug sensitivity profile,immunophenotyping) [Time frame: up to 7 years]
Secondary outcome measures (2)
- to study the resistance to treatments [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. [Time frame: up to 7 years]
Eligibility criteria
Inclusion criteria
- Diagnosis of acute leukemia, myelodysplastic syndrome, chronic myelomonocytic leukemia (CMML) or myeloproliferative syndrome according to the WHO classification 2016,
- Patient for whom a new line of therapy is initiated.
- Patient older than 18 years of age.
- Patient affiliated to the social security system or benefiting from such a system.
- Signed consent to participate.
Exclusion criteria
- Weight at inclusion < 50 kg
- Participating in another clinical study that would cause the total amount of blood collection to exceed the and endanger the patient
- Person in an emergency situation, adult under legal protection (guardianship, curatorship, etc.) protection (guardianship, curatorship or safeguard of justice), or unable to express his or her consent.
- Impossibility to submit to the medical follow-up of the trial for geographical social or psychological reasons,
- Pregnant or breastfeeding women
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT05602168 · HEMATOBIO.02-IPC 2021-061