Clinical trial · Interventional
Donor Lymphocyte Infusion (DLI) for Relapsed (Post Transplant) Leukemia
Treatment of Relapsed Leukemia After Allogeneic Bone Marrow Transplantation Using Donor-derived Lymphocytes
NCT00167167CI-TRIAL-00030599completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In this study our hypothesis is that infusion of donor lymphocyte immune cells from the subject's bone marrow donor will activate the subject's immune system to attack their cancer.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| AML | Acute Myeloid Leukemia | CURATED_BROADER | 0.80 |
| Leukemia, Lymphocytic, Acute | Leukemia | ONTOLOGY_EXACT | 0.85 |
| Leukemia, Myeloid, Chronic | Leukemia | ONTOLOGY_EXACT | 0.85 |
| MDS | Myelodysplastic Syndrome | CURATED_BROADER | 0.80 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Donor Lymphocyte Infusion | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- BMT patients
- description
- All patients treated.
- interventionNames
- Procedure: Donor Lymphocyte Infusion
Primary outcomes (1)
- measure
- Freedom of Disease: Bone marrow histology, cytogenetic analysis and RFLP will be studied. Data will be collected and tabulated.
- timeFrame
- before, at 3 months, 6 months, 9 months and 12 months after donor lymphocyte infusions
Secondary outcomes (4)
- measure
- Toxicity
- timeFrame
- during the infusion and immediately thereafter
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Year
- Maximum age
- 60 Years
Show eligibility criteria text
Inclusion Criteria: * Patients with CML, AML, MDS or ALL relapsed after related or unrelated donor allogeneic marrow transplantation. * Patients must be within one year of identification of relapse or if beyond that time period, must have some evidence of donor DNA by RFLP or cytogenetics. * Patients may have evidence of relapse based on molecular, cytogenetic or morphologic criteria. * CML patients must have cytogenetic evidence of relapse or if Ph negative to start, obvious evidence of relapse other than minimal residual disease. * Patients must have \<30% marrow blasts on a marrow biopsy performed within two weeks of the first donor lymphocyte infusion. * Patients with \>30% blasts can become eligible for donor lymphocytes after reinduction with any standard therapy regimen. * Patients with AML, MDS or ALL achieving a CR with standard therapy regimens are eligible for this protocol. * Patients who relapse with their initial disease or develop a second malignancy after related or unrelated donor allogeneic marrow transplantation with other initial diagnoses (such as but not limited to CLL, lymphoma, myeloma, juvenile CML, sarcoma, breast cancer) may also be included in this protocol. Patients will be eligible with or without other adjunct chemotherapy or radiation therapy. Post-transplant lymphomas (often referred to as EBV-associated lymphomas) will be eligible for donor leukocyte infusions on this protocol. Treatment with donor leukocytes under this protocol is restricted to malignant diseases only. Graft failure or relapse of non-malignant disorders is excluded from receiving donor leukocyte infusions on this protocol. Autologous transplant patients who relapse are not eligible for this protocol. Patients with malignant diseases amenable to other curative therapy are not eligible (i.e. skin cancers). Exclusion Criteria: * Patients with concurrent signs of acute or chronic graft-versus-host disease requiring ongoing treatment at the time of relapse will be ineligible. * Patients with \>30% marrow blasts at the time of therapy will be ineligible. * Patients on prednisone, cyclosporine, Imuran or other immunosuppressive medications are not eligible until these medications are discontinued for at least 2 weeks without a flare of GVHD. * CML patients in complete cytogenetic remission who are bcr/abl positive by PCR only are not eligible.
References
Publications (0)
Data not yet available
No reference posted for this study.