Innate Donor Effector Allogeneic Lymphocyte Infusion After Stem Cell Transplantation: the IDEAL Trial

ConditionAML/MDS
Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18-80
SponsorRigshospitalet, Denmark

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 volunteers

Qualifiers

Diagnoses: AML, MDS

Age: ≥18 years

Graft type: PBSC

Donor: ≥18 years

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • iDLI

    Other intervention

    TCRab/CD19 depleted DLI 14 days after allogeneic stem cell transplantation. Targeted cell doses: \>10e7 NK cells/kg and \>10e6 TCRgd cells/kg

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Innate donor lymphocyte infusion (iDLI)Experimental treatment 1 intervention
Group B: Standard of careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Relapse-free survival

Relapse-free survival

Time frame
1 year from transplantation
2

aGVHD

Acute graft-versus-host-disease grade 2-4

Time frame
100 days from transplantation

Secondary outcomes

1

iDLI dose

Number of infused NK cells and TCR γδ cells in the iDLI product.

Time frame
14 days from transplantation
2

iDLI phenotype

Immune phenotype of infused NK cells and TCR γδ cells in the iDLI product.

Time frame
14 days from transplantation
3

Neutrophil engraftment

Neutrophil engraftment

Time frame
100 days from transplantation

Other outcomes

1

Stem cell graft dose

Doses of transplanted stem cells (CD34) and lymphocyte subsets in the graft product

Time frame
During procedure
2

Stem cell graft phenotype

Immune phenotypes of transplanted stem cells (CD34) and lymphocyte subsets in the graft product

Time frame
During procedure
3

Immune reconstitution cell doncentrations

Concentrations of lymphocyte subset in peripheral blood of patients during immune reconstitution

Time frame
14-91 days from transplantation
4

Immune reconstitution phenotype

Immune phenotypes of lymphocyte subset in peripheral blood of patients during immune reconstitution

Time frame
14-91 days from transplantation

Sponsors and contacts

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