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Related donor transplants: Has posttransplantation cyclophosphamide nullified the detrimental effect of HLA mismatch?

  • Acute Leukemia Working Party of the European Society for Blood and Marrow Transplant
  • , Center for International Blood and Marrow Transplant Research
  • Johns Hopkins University
  • Medical College of Wisconsin
  • Sorbonne Université
  • Institut Paoli Calmettes
  • Northside Hospital
  • Institut de Cancérologie Gustave Roussy
  • San Raffaele Scientific Institute
  • University of Texas MD Anderson Cancer Center
  • Ohio State University
  • Bordeaux University Hospital
  • CellMED Consulting
  • Oxford University Hospitals NHS Foundation Trust
  • Washington University St. Louis
  • Université Paris Cité
  • CHU de Lille
  • Dana-Farber Cancer Institute

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

We sought to identify whether posttransplantation cyclophosphamide (PT-Cy) reduces or eliminates the detrimental impact of HLA mismatching on outcomes of HLA-haploidentical related donor transplantation for acute leukemia. Data from 2143 donor-recipient pairs (n = 218 haploidentical sibling; n = 218 offspring; n = 1707 HLA-matched sibling) with acute myeloid or lymphoblastic leukemia were studied. All received a calcineurin inhibitor for graft-versus-host disease (GVHD) prophylaxis while high-dose PT-Cy was also given to recipients of haploidentical transplant. Patient age correlated with donor-recipient relationship: haploidentical siblings donated to patients aged 18 to 54 years whereas offspring donated to patients aged 55 to 76 years. Therefore, transplant outcomes were examined separately in the 2 patient age groups. In patients aged 18 to 54 years, there were no significant differences in outcomes except chronic GVHD, which was lower after haploidentical sibling compared to HLA-matched sibling transplant (hazard ratio [HR], 0.63; P, .001). In patients aged 55 to 76 years, despite lower chronic GVHD (HR, 0.42; P, .001), graft failure (14% vs 6%; P = .003), nonrelapse mortality (HR, 1.48; P = .02), and overall mortality (HR, 1.32; P = .003) were higher after transplant from offspring compared with an HLA-matched sibling. These data demonstrate a superior outcome in older recipients when using an HLA-matched sibling instead of offspring, although there were differences in transplant platforms (GVHD prophylaxis and graft type) between the 2 groups. Validation of these findings requires a prospective randomized trial wherein the transplant platforms can be closely matched.

Original languageEnglish
Pages (from-to)1180-1186
Number of pages7
JournalBlood advances
Volume2
Issue number11
DOIs
StatePublished - 12 Jun 2018

Funding

FundersFunder number
National Cancer InstituteU24CA076518

    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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