| Literature DB >> 29794073 |
Tara M Robinson1, Ephraim J Fuchs1, Mei-Jie Zhang2, Andrew St Martin3, Myriam Labopin4, Daniel A Keesler3, Didier Blaise5, Asad Bashey6, Jean-Henri Bourhis7, Fabio Ciceri8, Stefan O Ciurea9, Steven M Devine10, Mohamad Mohty4, Shannon R McCurdy1, Noel Milpied11, Ian K McNiece12, Vanderson Rocha13, Rizwan Romee14, Gerard Socie15, Ibrahim Yakoub-Agha16, Robert J Soiffer17, Mary Eapen3, Arnon Nagler18.
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.Entities:
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Year: 2018 PMID: 29794073 PMCID: PMC5998932 DOI: 10.1182/bloodadvances.2018018291
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529