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Alternative donors for allogeneic hematopoietic stem cell transplantation in poor-risk AML in CR1

  • on behalf of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation (EBMT)
  • University Medical Center Rotterdam
  • Erasmus University Rotterdam
  • Sorbonne Université
  • Institut national de la santé et de la recherche médicale
  • Assistance Publique–Hopitaux de Paris
  • Hématologie Clinique et Thérapie Cellulaire
  • Eurocord
  • Université Paris Cité
  • Unité mixte de recherche 1160
  • Department of Hematology
  • Department of Hematology
  • Soochow University
  • Division of Cardiology
  • Helsinki University Hospital
  • Department of Hematology and Transplant Program
  • Institut Paoli Calmettes
  • Department of Hematology
  • Hôpital du Haut-Lévêque
  • Centre for Clinical Haematology
  • University Hospitals Birmingham NHS Foundation Trust
  • Department of Hematology
  • Lille University School of Medicine
  • Department of Hematology
  • KU Leuven
  • Dept. of Hematology
  • Karolinska Institutet
  • Department of Hematology
  • CHU de Toulouse
  • Department of Hematology
  • Hospices civils de Lyon
  • Department of Hematology
  • Hôpital Jean Minjoz
  • Department of Haematology
  • Service de Cardiologie
  • University of Basel
  • Hematology and Bone Marrow Transplantation Unit
  • IRCCS San Raffaele Scientific Institute
  • Sheba Medical Center at Tel Hashomer

Research output: Contribution to journal › Article › peer-review

81 Scopus citations

Abstract

Allogeneic hematopoietic stem cell transplantation (alloHSCT) remains the treatment of choice to consolidate remission in patients with poor-risk acute myeloid leukemia (AML). With increasing alternative donors available, the preferred donor or stem cell source is debated. We set out to study outcome in recipients of alloHSCT with poor-risk AML in first complete remission (CR1) by donor type. A total of 6545 adult patients with poor-risk AML in CR1 receiving an alloHSCT using matched related donor (MRD, n 5 3511) or alternative donors, including 10/10 (n 5 1959) or 9/10 matched unrelated donors (MUDs, n 5 549), umbilical cord blood (UCB) grafts (n 5 333), or haplo-identical (haplo) donors (n 5 193) were compared. Overall survival (OS) at 2 years following MRD alloHSCT was an estimated 59 6 1%, which did not differ from 10/10 MUD (57 6 1%) and haplo alloHSCT (57 6 4%). OS, however, was significantly lower for 9/10 MUD alloHSCT (49 6 2%) and UCB grafts (44 6 3%), respectively (P, .001). Nonrelapse mortality (NRM) depended on donor type and was estimated at 26 6 3% and 29 6 3% after haplo alloHSCT and UCB grafts at 2 years vs 15 6 1% following MRD alloHSCT. Multivariable analysis confirmed the impact of donor type with OS following MRD, 10/10 MUD, and haplo alloHSCT not being statistically significantly different. NRM was significantly higher for alternative donors as compared with MRD alloHSCT. Collectively, these results suggest that alloHSCT with MRDs and 10/10 MUDs may still be preferred in patients with poor-risk AML in CR1. If an MRD or 10/10 MUD is not available, then the repertoire of alternative donors includes 9/10 MUD, UCB grafts, and haplo-identical donors. The latter type of donor is increasingly applied and now approximates results with matched donors.

Original languageEnglish
Pages (from-to)477-485
Number of pages9
JournalBlood Advances
Volume1
Issue number7
DOIs
StatePublished - 28 Feb 2017
Externally publishedYes

Funding

Funders
American Society for Blood and Marrow Transplantation

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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