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

Authors :
Robinson TM
Fuchs EJ
Zhang MJ
St Martin A
Labopin M
Keesler DA
Blaise D
Bashey A
Bourhis JH
Ciceri F
Ciurea SO
Devine SM
Mohty M
McCurdy SR
Milpied N
McNiece IK
Rocha V
Romee R
Socie G
Yakoub-Agha I
Soiffer RJ
Eapen M
Nagler A
Source :
Blood advances [Blood Adv] 2018 Jun 12; Vol. 2 (11), pp. 1180-1186.
Publication Year :
2018

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.<br /> (© 2018 by The American Society of Hematology.)

Details

Language :
English
ISSN :
2473-9537
Volume :
2
Issue :
11
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
29794073
Full Text :
https://doi.org/10.1182/bloodadvances.2018018291