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In patients undergoing HCT, the optimal donor choice has historically been an HLA-matched sibling donor; however, this is only typically available for up to 30% of patients.1 Prioritization of a donor in the absence of a matched sibling is based on HLA-matching and non-HLA factors including donor age, CMV matching, sex matching, and donor parity.1
A study by the Center for International Blood & Marrow Transplant Research (CIBMTR), published in Blood Advances, employed a novel statistical approach using advanced machine learning (NFT BART) to analyze the impact of donor characteristics on post-HCT outcomes, with the aim of improving donor selection.1 A total of 11,818 patients, with a median age of 57 years, who received allo-HCT from HLA-matched (8/8) unrelated donors between 2016 and 2019 were included in the study. The NFT-BART model was trained using ~85% of the study population and validated using the remaining population.1 |
Key learnings |
In this observational study, use of donors aged 18–30 years offered optimal outcomes, with a significant reduction in OS observed with donors aged ≥31 years. Improved EFS was found with the use of donors aged 18 years compared with donors aged ≥32 years. |
A clinically meaningful impact was defined as >1% difference in predicted outcome (OS or EFS) at 3 years; donor CMV, parity, HLA-DQB1 and HLA-DPB1 T cell epitope matching were not found to have a meaningful impact. |
Male donors were associated with meaningful improvement in EFS compared with female donors; however, sex had no significant effect on OS, allowing clinicians flexibility in donor selection without compromising survival outcomes. |
To improve outcomes following HCT, the first available donor aged 18–30 years should be used, with a male donor preferred if multiple donors are available. |
Abbreviations: CMV, cytomegalovirus; EFS, event-free survival; HCT, hematopoietic cell transplantation; HLA, human leukocyte antigen; NFT-BART, Nonparametric Failure Time Bayesian Additive Regression Trees; OS, overall survival.
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