Clinical Research
Similar Transplantation Outcomes for Acute Myeloid Leukemia and Myelodysplastic Syndrome Patients with Haploidentical versus 10/10 Human Leukocyte Antigen–Matched Unrelated and Related Donors

https://doi.org/10.1016/j.bbmt.2014.08.013Get rights and content
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Highlights:

  • Comparable progression-free survival for patients with acute myeloid leukemia and myelodysplastic syndromes treated with a haploidentical versus an HLA-matched donor.

  • Similar recovery of the immune function after transplantation for haploidentical versus matched related or unrelated donor transplantations.

Abstract

Allogeneic stem cell transplantation for patients with acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) has been performed primarily with an HLA-matched donor. Outcomes of haploidentical transplantation have recently improved, and a comparison between donor sources in a uniform cohort of patients has not been performed. We evaluated outcomes of 227 patients with AML/MDS treated with melphalan-based conditioning. Donors were matched related (MRD) (n = 87, 38%), matched unrelated (MUD) (n = 108, 48%), or haploidentical (n = 32, 14%). No significant differences were found between haploidentical and MUD transplantation outcomes; however, there was a trend for improved outcomes in the MRD group, with 3-year progression-free survival for patients in remission of 57%, 45%, and 41% for MRD, MUD, and haploidentical recipients, respectively (P = .417). Recovery of T cell subsets was similar for all groups. These results suggest that haploidentical donors can safely extend transplantation for AML/MDS patients without an HLA-matched donor. Prospective studies comparing haploidentical and MUD transplantation are warranted.

Key Words

Myeloablative reduced-intensity conditioning regimen
Fludarabine-melphalan
Hematopoietic stem cell transplantation
Acute myeloid leukemia
Myelodysplastic syndromes
Haploidentical transplantation
Post-transplantation cyclophosphamide

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Financial disclosure: See Acknowledgments on page 1980.