4.2 Article

ATG in HLA-Matched, Peripheral Blood, Hematopoietic Cell Transplantation in Acute Myeloid Leukemia and Myelodysplastic Syndrome: A Secondary Analysis of a CIBMTR Database

Journal

TRANSPLANTATION AND CELLULAR THERAPY
Volume 29, Issue 1, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jtct.2022.09.010

Keywords

ATG peripheral blood stem cells; HLA-matched hematopoietic cell transplantation; CIBMTR

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This study analyzed the impact of anti-T-cell globulin (ATG) in HLA-matched and unrelated donor peripheral blood stem cell transplantation (PBSC HCT). The results showed that ATG can reduce the occurrence of chronic graft-versus-host disease (GVHD) and improve the quality of life of patients, but it may increase the relapse rate. Therefore, ATG should be considered as a standard treatment in this population.
Peripheral blood stem cells (PBSC) are the preferred grafts for hematopoietic cell transplantation (HCT), according to the CIBMTR. Donor recovery is faster with PBSC harvest, but PBSC is associated with higher chronic graft-versus-host disease (GVHD) and poorer quality of life. Anti-T-cell globulin (ATG) is polyclonal IgG from rabbits or horses immunized with human thymocytes or a human T-cell line, which may reduce GVHD in HCT and improve outcomes. The objective of this study was to analyze the impact of ATG in HLA-matched related (MRD) and matched (HLA 8/8) unrelated donor (MUD) HCT. We used a freely available CIBMTR database published online for secondary analyses. The database included patients similar to 40 years old who have undergone their first PBSCMRD or MUD HCT for acute myeloid leukemia or myelodysplastic syndrome with or without ATG between 2008 and 2017. Patients who received posttransplant cyclophosphamide or alemtuzumab were excluded. Overall survival was not different with ATG (hazard ratio [HR] = 1.09; 95% confidence interval [CI], 1.00-1.19; P =.06) comparedwith no ATG. Relapse rate was higher with ATG (HR = 1.29; 95% CI, 1.17-1.43; P <.001) and non-relapse mortality was lower with ATG (HR = 0.84; 95% CI, 0.72-0.98; P =.03). Grades II-IV acute GVHD was significantly lower with ATG (HR = 0.77; 95% CI, 0.69-0.87; P <.001) but not grades III-IV acute GVHD (HR = 0.85; 95% CI, 0.69-1.04; P =.11). Both chronic GVHD (HR = 0.54; 95% CI, 0.48-0.60; P <.001) and moderate/severe chronic GVHD (HR = 0.45; 95% CI, 0.38-0.52; P <.001) were lower with ATG. There was an interaction between ATG and conditioning regimen for relapse rate and overall survival. Relapse rate was higher in those who received reduced-intensity (RIC) or non-myeloablative (NMA) conditioning regimens and ATG, compared with MAC +/- ATG or RIC without ATG (interaction test, P =.003). Overall survival was also poorer with ATG and RIC or NMA conditioning regimens (interaction test, P =.03). Our results show that ATG can mitigate the more severe forms of chronic GVHD without impairing overall survival in HLA-matched HCT with PBSC grafts and myeloablative conditioning regimen. ATG should be standard in this population. (c) 2023 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved. (c) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

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