Effect of donor age in patients with acute myeloid leukemia undergoing haploidentical hematopoietic cell transplantation vary by conditioning intensity and recipient age

Author:

Saliba Rima M.1,Kanakry Christopher G.2,Gadalla Shahinaz3,Kebriaei Partow1,Rezvani Katayoun1,Champlin Richard E.1,Shpall Elizabeth J.1,Weisdorf Daniel4ORCID,Mehta Rohtesh S.5ORCID

Affiliation:

1. Department of Stem Cell Transplantation and Cellular Therapy The University of Texas MD Anderson Cancer Center Houston Texas USA

2. Center for Immuno‐Oncology, Center for Cancer Research, National Cancer Institute National Institutes of Health Bethesda Maryland USA

3. Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda Maryland USA

4. Division of Hematology, Oncology and Transplantation, Department of Medicine University of Minnesota Minneapolis Minnesota USA

5. Clinical Research Division, Adult Blood and Marrow Transplantation Fred Hutchison Cancer Center Seattle Washington USA

Abstract

AbstractWe investigated the impact of donor age (younger [≤35 years] vs. older [>35 years]) after accounting for other non‐HLA and HLA factors on outcomes of patients with acute myeloid leukemia undergoing HLA‐haploidentical hematopoietic cell transplantation (n = 790). The effect differed by conditioning—partly related to the differences in the recipient age in myeloablative (MAC; median 46 years) versus reduced‐intensity/non‐myeloablative conditioning (RIC/NMA; median 61 years) groups. With MAC (n = 320), donor age had no impact on acute graft‐versus‐host disease (GVHD), but older donors were associated with a significantly higher risk of chronic GVHD (hazard ratio [HR]: 1.6, 95% confidence interval [CI]: 1.10–2.30, p = .02) independent of recipient age and other factors. Donor age had no impact on either relapse or non‐relapse mortality (NRM). The impact of donor/recipient age on overall survival changed over time. Older donors were associated with significantly higher late overall mortality (>6 months) in younger recipients (≤ 50 years; HR: 2.2, 95% CI: 1.03–4.6, p = .04) but not older recipients. With RIC/NMA (n = 470), neither recipient's nor donor's age influenced the risk of GVHD. Donor age had no significant impact on the risk of relapse, but older donors were associated with a significantly higher risk of NRM (HR: 1.6, 95% CI: 1.02–2.6, p = .04) independent of recipient age. Older donor age was associated with significantly higher late overall mortality (>9 months) in older recipients (>50 years; HR: 1.66, 95% CI: 1.0–2.67; p = .049) but not in younger recipients. Donor selection based on donor age may require a tailored approach for a particular recipient.

Publisher

Wiley

Subject

Hematology

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