| Literature DB >> 31582392 |
Scott R Solomon1, Andrew St Martin2, Nirav N Shah3, Giancarlo Fatobene4, Monzr M Al Malki5, Karen K Ballen6, Asad Bashey1, Nelli Bejanyan7, Javier Bolaños Meade8, Claudio G Brunstein9, Zachariah DeFilipp10, Richard E Champlin11, Ephraim J Fuchs8, Mehdi Hamadani2, Peiman Hematti12, Christopher G Kanakry13, Joseph P McGuirk14, Ian K McNiece15, Stefan O Ciurea11, Marcelo C Pasquini2, Vanderson Rocha4,16, Rizwan Romee17, Sagar S Patel18, Sumithira Vasu19, Edmund K Waller20, John R Wingard21, Mei-Jie Zhang2, Mary Eapen2.
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.Entities:
Year: 2019 PMID: 31582392 PMCID: PMC6784523 DOI: 10.1182/bloodadvances.2019000627
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529