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Updated: Jan 4, 2026

Competitive Transplants to Evaluate Hematopoietic Stem Cell Fitness
Published on: August 31, 2016
Improved survival after offspring donor transplant compared with older aged-matched siblings for older leukaemia
Yu Wang1,2, Qi-Fa Liu3, De-Pei Wu4,2
1Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Insights
For older leukemia patients, using a younger offspring donor for hematopoietic cell transplant (HCT) significantly improves survival compared to an older matched sibling donor (MSD). Offspring donors lead to better overall and leukemia-free survival with lower transplant-related mortality.
Area of Science:
- Hematology
- Oncology
- Transplant Immunology
Background:
- Donor selection for hematopoietic cell transplant (HCT) in older acute leukemia patients (≥50 years) is not well-defined.
- Outcomes may differ based on donor type, with potential advantages for younger offspring donors over older human leukocyte antigen (HLA)-matched sibling donors (MSD).
Purpose of the Study:
- To compare outcomes of HCT in older acute leukemia patients receiving grafts from offspring donors versus HLA-matched sibling donors.
- To determine if donor characteristics beyond HLA matching, such as age and kinship, influence transplant success.
Main Methods:
- A multicenter dataset of 185 acute leukemia patients (≥50 years) transplanted in first complete remission was analyzed.
- A 1:1 matched-pair analysis compared outcomes between 54 patients receiving HCT from offspring donors and 54 matched patients receiving HCT from MSDs.
- Key outcomes assessed included graft-versus-host disease (GVHD), transplant-related mortality, relapse incidence, overall survival, and leukemia-free survival (LFS).
Main Results:
- Graft-versus-host disease incidence was comparable between offspring and MSD groups (acute: 26% vs. 35%; chronic: 37% vs. 24%).
- Offspring HCT demonstrated significantly lower 3-year transplant-related mortality (9% vs. 26%; P=0.023) and higher overall survival (85% vs. 58%; P=0.003) and LFS (85% vs. 56%; P=0.001) compared to MSD HCT.
- Relapse incidence was lower with offspring donors (6% vs. 17%; P=0.066).
Conclusions:
- Younger offspring donors may be favored over older MSDs for HCT in patients over 50 years old with acute leukemia.
- Non-HLA donor characteristics, including kinship and donor age, appear to be predominant factors influencing survival in this patient population.
- These findings suggest a re-evaluation of donor selection criteria for older leukemia patients undergoing HCT.
Abstract:
Donor selection for older leukaemia patients undergoing haematopoietic cell transplant (HCT) is not well defined: outcomes might be improved with a younger offspring donor rather than an older human leukocyte antigen (HLA)-matched sibling donor (MSD). We extended our multicentre dataset. A total of 185 acute leukaemia patients (≥ 50 years) transplanted in first complete remission who received HCT from offspring (n = 62) or MSD (n = 123) were included. A 1:1 ratio matched-pair analysis was performed. We were able to match 54 offspring with 54 MSD patients. Outcomes were compared between the two matched-pair groups. The cumulative incidence of grade II/IV acute graft-versus-host disease (GVHD) (26% vs. 35%; P = 0·23) and chronic GVHD (37% vs. 24%; P = 0·19) was comparable between groups (MSD vs. offspring). The lower three-year transplant-related mortality (9% vs. 26%; P = 0·023) and relapse incidence (6% vs. 17%; P = 0·066) resulted in higher overall survival (85% vs. 58%; P = 0·003) and leukaemia-free survival (LFS) (85% vs. 56%; P = 0·001) in offspring HCT compared with that in MSD HCT. These data might favour a young offspring over an older MSD in patients >50 years. The current analyses confirm that non-HLA donor characteristics, such as kinship and donor age, rather than HLA disparity, predominantly influence survival in older acute leukaemia patients.
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