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Myeloablative vs reduced intensity T-cell-replete haploidentical transplantation for hematologic malignancy.

Authors :
Solomon SR
St Martin A
Shah NN
Fatobene G
Al Malki MM
Ballen KK
Bashey A
Bejanyan N
Bolaños Meade J
Brunstein CG
DeFilipp Z
Champlin RE
Fuchs EJ
Hamadani M
Hematti P
Kanakry CG
McGuirk JP
McNiece IK
Ciurea SO
Pasquini MC
Rocha V
Romee R
Patel SS
Vasu S
Waller EK
Wingard JR
Zhang MJ
Eapen M
Source :
Blood advances [Blood Adv] 2019 Oct 08; Vol. 3 (19), pp. 2836-2844.
Publication Year :
2019

Abstract

In the absence of prospective studies that examine the effect of conditioning regimen intensity after T-cell-replete haploidentical transplant for acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), and myelodysplastic syndrome (MDS), a retrospective cohort analysis was performed. Of the 1325 eligible patients (AML, n = 818; ALL, n = 286; and MDS, n = 221), 526 patients received a myeloablative regimen and 799 received a reduced-intensity regimen. Graft-versus-host disease prophylaxis was uniform with posttransplant cyclophosphamide, a calcineurin inhibitor, and mycophenolate mofetil. The primary end point was disease-free survival. Cox regression models were built to study the effect of conditioning regimen intensity on transplant outcomes. For patients aged 18 to 54 years, disease-free survival was lower (hazard ratio [HR], 1.34; 42% vs 51%; P = .007) and relapse was higher (HR, 1.51; 44% vs 33%; P = .001) with a reduced-intensity regimen compared with a myeloablative regimen. Nonrelapse mortality did not differ according to regimen intensity. For patients aged 55 to 70 years, disease-free survival (HR, 0.97; 37% vs 43%; P = .83) and relapse (HR, 1.32; 42% vs 31%; P = .11) did not differ according to regimen intensity. Nonrelapse mortality was lower with reduced-intensity regimens (HR, 0.64; 20% vs 31%; P = .02). Myeloablative regimens are preferred for AML, ALL, and MDS; reduced-intensity regimens should be reserved for those unable to tolerate myeloablation.

Details

Language :
English
ISSN :
2473-9537
Volume :
3
Issue :
19
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
31582392
Full Text :
https://doi.org/10.1182/bloodadvances.2019000627