About this trial
The curative principle behind allogeneic hematopoietic stem cell transplantation (HSCT) is eradication of the malignant cells of the patient (recipient) by donor graft cells, a process termed graft-versus-leukemia (GVL) effect. GVL is traditionally mediated by donor αβ T cells in an immunological process driven by genetical differences between individuals, i.e. an allogeneic response. For this reason, αβ T cells also cause an unwanted and dangerous complication of HSCT called graft-versus-host disease (GVHD) in which healthy recipient cells are targeted by donor cells with great risk of morbidity and mortality to the patient. In addition to αβ T cells, other cells from the donor stem cell graft, termed innate effector lymphocytes, can contribute to the GVL effect. These are termed natural killer (NK) cells and T-cell receptor (TCR) γδ cells, the latter being a subset of T cells. NK and TCR γδ cells can recognize and eliminate leukemic cells in a direct tumor response independent of conventional allogeneicity. Therefore, opposite αβ T cells, innate effector lymphocytes cells can mediate GVL but are not likely to cause GVHD. The main indications for HSCT in adults are acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Approximately 50% of AML/MDS transplant patients experience significant acute GVHD and 30% experience relapse of the malignant disease. Prospective clinical studies from the research group of the investigators have shown that patients with high doses of innate lymphocytes in stem cell grafts and during early immune reconstitution after HSCT have a reduced risk of both GVHD and relapse. The aim of this clinical trial is therefore to administer innate donor lymphocyte infusion (iDLI) enriched in NK and TCR γδ cells and depleted of αβ T cells in patients early after HSCT. By improving the HSCT procedure with iDLI cell therapy the scope is less GVHD and less relapse of the malignant disease and thereby improved survival and life quality in AML/MDS patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Diagnoses: AML, MDS
Age: ≥18 years
Graft type: PBSC
Donor: ≥18 years
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
iDLI
Other interventionTCRab/CD19 depleted DLI 14 days after allogeneic stem cell transplantation. Targeted cell doses: \>10e7 NK cells/kg and \>10e6 TCRgd cells/kg
Treatment groups
Trial outcomes
Primary outcomes
Relapse-free survival
Relapse-free survival
aGVHD
Acute graft-versus-host-disease grade 2-4
Secondary outcomes
iDLI dose
Number of infused NK cells and TCR γδ cells in the iDLI product.
iDLI phenotype
Immune phenotype of infused NK cells and TCR γδ cells in the iDLI product.
Neutrophil engraftment
Neutrophil engraftment
Other outcomes
Stem cell graft dose
Doses of transplanted stem cells (CD34) and lymphocyte subsets in the graft product
Stem cell graft phenotype
Immune phenotypes of transplanted stem cells (CD34) and lymphocyte subsets in the graft product
Immune reconstitution cell doncentrations
Concentrations of lymphocyte subset in peripheral blood of patients during immune reconstitution
Immune reconstitution phenotype
Immune phenotypes of lymphocyte subset in peripheral blood of patients during immune reconstitution
Sponsors and contacts
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