Overview
The investigators have previously shown the absence of toxicity of Treg-depleted-DLI and the possibility to triggering alloreactivity (GVHD/GVT) in relapsing patients dealing with hematological malignancies who had never shown any signs of GVHD after transplant or after one or more DLI.
The Investigators, we plan to demonstrate the benefit of Treg-depleted DLI as compared to the reference treatment of relapse in hematological malignancies after allogeneic HSCT which is currently based on standard DLI
Description
This clinical trial is designed to demonstrate the benefit of Treg-depleted DLI as compared to the reference treatment of relapse in hematological malignancies after allogeneic HSCT which is currently based on standard DLI.
Patients who have never shown any signs of GVHD and for which one (or more) unmanipulated DLI have been ineffective. Those patients will receive a subsequent DLI, which will be either unmanipulated (control arm) or Treg depleted (experimental arm) after a randomization. In both cases, the second DLI will be immediately preceded by a lymphodepleting treatment based on cyclophosphamide and fludarabine association.
Eligibility
Inclusion Criteria:
- Children and adults regardless of age or weight allograft for primary or secondary acute leukemia, MDS, lympho-proliferative syndrome (CLL, Myeloma, Lymphoma) or myelo-proliferative syndrome.
- Prior allogeneic HSCT (myeloablative or non-myeloablative conditioning) from a family donor geno-identical HLA or a volunteer donor HLA 10/10 or 9/10.
- Molecular, cytogenetic, cytological relapse regardless of the date after the transplant.
- Previous standard DLI should have brought a total dose of at least 5.10^6 CD3 + / kg (donor HLA-geno idendique) or 2.10^6 CD3 + / kg (voluntary donor) or 5.10^5 CD3+/kg (donor haplo-idendique).
- Patient corresponding to the failure criteria of a previous standard DLI, defined for each type of hematological malignancies in the test model "DLI-Treg-1" after a delay of at least 30 days in the case of a progressive disease after DLI and at least 60 days in the case of stable disease (due to possible delayed responses after DLI).
- Patient consented to the study (the consent of both parents will be collected for minors)
- Patients insured by a social security system.
- Negative pregnancy test (β-HCG hormone) within the 7 days prior to enrollment
Exclusion Criteria:
- Presence of acute GVHD grade> II or extensive chronic GVHD since the first DLI
- Patient receiving immunosuppressive therapy for the treatment of GVHD or other reason
- Impairment of liver function (transaminases> 5 N or bilirubin> 50 µM except Gilbert's disease) or renal function (creatinine clearance <30 ml / min)
- OMS performance status > 2
- Non controlled severe infection
- Patient under tutorship, curatorship or legal protection
Donor Inclusion Criteria
- Being the initial HSC donor (HLA geno-identical family or haplo-identique or non-family HLA 10/10 or 9/10)
- Weight ≥20 kg authorizing the lymphapheresis
- Having no contra-indications for donating blood
- Absence of severe heart failure, unstable heart disease, uncontrolled hypertension, type 1 diabetes
- Negative serology for HIV1-2, HBV, HCV, HTLV 1 and VDRL/TPHA in the 30 days prior to apheresis. Negative viral genomics diagnosis is required for HIV, HBV and HCV
- Being informed of the study, and have given an oral non opposition