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Updated: Mar 30, 2026

Author Spotlight: Identification and Isolation of Quiescent Leukemia Stem Cells from Zebrafish T-ALL
Published on: July 19, 2024
[Donor cell leukemia (DCL): A prospective study of its identification and treatment]
Guillermo J Ruiz-Delgado1,2,3, Jesús Hernández-Reyes1,4, Mónica Patricia González-Ramírez1,5
1Centro de Hematología y Medicina Interna, Clínica Ruiz de Puebla, Puebla, Pue., México.
Insights
Donor cell leukemia, a rare complication of stem cell transplants, may be more common than previously thought. Prompt chemotherapy offers a chance for remission in these patients.
Area of Science:
- Hematology
- Oncology
- Transplantation Immunology
Context:
- Donor-derived malignancies are rare post-transplant complications.
- Allogeneic hematopoietic stem cell transplantation (HSCT) and solid organ transplantation (SOT) carry risks.
- Donor cell leukemia (DCL) is an exceptionally rare entity.
Purpose:
- To prospectively investigate the incidence of DCL in leukemia patients undergoing HSCT.
- To evaluate the efficacy of a pediatric-inspired chemotherapy regimen for DCL.
- To assess outcomes and long-term status of DCL survivors.
Summary:
- Seven cases of DCL were identified over 12 years in 106 leukemia patients receiving HSCT.
- Six cases involved donor cell acute lymphoblastic leukemia (ALL), treated with combined chemotherapy.
- Three of six DCL patients achieved complete response; survivors remained full chimeras without needing a second transplant.
Impact:
- Suggests the incidence of DCL may be underestimated.
- Demonstrates the potential for favorable responses to combined chemotherapy in DCL.
- Highlights the possibility of long-term survival without further transplantation for DCL patients.
Abstract:
Donor-derived malignancies after allogeneic hematopoietic stem cell transplantation and after solid organ transplantation are considered as rare diseases. We have prospectively searched for donor cell leukemia in a 12-year period, in a single institution, in a group of 106 consecutive patients allografted because of leukemia. We have identified seven cases of donor cell leukemia; six were allografted because of relapsed acute lymphoblastic leukemia and one because of paroxysmal nocturnal hemoglobinuria/aplastic anemia. These figures suggest that the real incidence of donor cell leukemia has been underestimated. The six patients with lymphoblastic donor cell leukemia were treated prospectively with a pediatric-inspired combined chemotherapy schedule designed for de novo acute leukemia. A complete response was obtained in three out of six patients with lymphoblastic donor cell leukemia. It is possible to obtain favorable responses in donor cell leukemia patients employing combined chemotherapy. The long-term donor cell leukemia survivors remain as full chimeras and have not needed a second transplant.
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