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Inferior Overall Survival After Haploidentical Donor Lymphocyte Infusions in Relapsed Myeloid Neoplasms
Tobias Matthieu Benoit1, Adrian Bachofner1, Nathan Wolfensberger1
1Department of Medical Oncology and Hematology, University Hospital Zurich, Zürich, Switzerland.
European Journal of Haematology
|November 6, 2024
Summary
Donor lymphocyte infusion (DLI) can treat relapsed myeloid neoplasms post-hematopoietic stem cell transplantation (HSCT). Haploidentical DLI showed inferior overall survival compared to HLA-identical DLI, suggesting alternative strategies are needed.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative option for high-risk myeloid neoplasms.
- Relapse post-HSCT, especially in acute myeloid leukemia (AML) and myelodysplastic neoplasms (MDS), remains a significant clinical challenge.
- Donor lymphocyte infusion (DLI) is used to manage relapses, but its efficacy and safety, particularly in haploidentical settings, require further elucidation.
Purpose of the Study:
- To evaluate the effectiveness and safety of DLI in patients with relapsed AML or MDS post-HSCT.
- To compare outcomes between HLA-identical and haploidentical DLI.
- To identify factors influencing overall survival (OS) and progression-free survival (PFS) after DLI.
Main Methods:
- Retrospective cohort study of 57 patients with AML or MDS receiving DLI post-HSCT (2002-2023).
- Included preemptive and therapeutic DLI applications.
- Endpoints assessed: OS, PFS, and graft-versus-host disease (GvHD) incidence.
Main Results:
- Median OS post-DLI was 517 days, with a 1-year OS of 62.5%.
- Factors associated with improved OS included younger patient age, HLA-identical donor, pre-HSCT treatment naivety, and preemptive DLI indication.
- Haploidentical DLI was linked to inferior OS compared to HLA-identical DLI, but PFS and GvHD incidence did not significantly differ.
Conclusions:
- Haploidentical DLI is associated with inferior OS in relapsed AML/MDS patients compared to HLA-identical DLI.
- The findings highlight limitations of haploidentical DLI in this context.
- Further research into alternative strategies, such as higher cell doses or combination therapies, is warranted.

