Blood Advances (Jun 2018)

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

  • Tara M. Robinson,
  • Ephraim J. Fuchs,
  • Mei-Jie Zhang,
  • Andrew St. Martin,
  • Myriam Labopin,
  • Daniel A. Keesler,
  • Didier Blaise,
  • Asad Bashey,
  • Jean-Henri Bourhis,
  • Fabio Ciceri,
  • Stefan O. Ciurea,
  • Steven M. Devine,
  • Mohamad Mohty,
  • Shannon R. McCurdy,
  • Noel Milpied,
  • Ian K. McNiece,
  • Vanderson Rocha,
  • Rizwan Romee,
  • Gerard Socie,
  • Ibrahim Yakoub-Agha,
  • Robert J. Soiffer,
  • Mary Eapen,
  • Arnon Nagler

Journal volume & issue
Vol. 2, no. 11
pp. 1180 – 1186

Abstract

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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.