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Should anti-thymocyte globulin be added in post-transplant cyclophosphamide based matched unrelated donor peripheral blood stem cell transplantation for acute myeloid leukemia? A study on behalf of the Acute Leukemia Working Party of the EBMT

  • Alexandros Spyridonidis*
  • , Myriam Labopin
  • , Eolia Brissot
  • , Ivan Moiseev
  • , Jan Cornelissen
  • , Goda Choi
  • , Fabio Ciceri
  • , Jan Vydra
  • , P. ter Reményi
  • , Montserrat Rovira
  • , Ellen Meijer
  • , H. lène Labussière-Wallet
  • , Didier Blaise
  • , Gwendolyn van Gorkom
  • , Nicolaus Kröger
  • , Yener Koc
  • , Sebastian Giebel
  • , Ali Bazarbachi
  • , Bipin Savani
  • , Arnon Nagler
  • Mohamad Mohty
*Corresponding author for this work
  • University of Patras
  • Sorbonne Université
  • Paris 6 University and APHP Hôpital Saint-Antoine
  • Hematology and Transplantation, Raisa Gorbacheva Research Institute of Pediatric Oncology, Pavlov University, St. Petersburg, Russia
  • Erasmus University Rotterdam
  • University of Groningen
  • From the Neuroimaging Research Unit, Division of Neuroscience (P.P.), and Neurology Unite (P.P.), IRCCS San Raffaele Scientific Institute, Milan, Italy; and Department of Anatomy and Neurosciences (M.M.S.), MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam UMC, Vrije Universiteit Amsterdam, the Netherlands
  • Institute of Hematology and Blood Transfusion
  • Dél-pesti Centrumkórház
  • Hospital Clinic de Barcelona
  • Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre Bénite, France
  • Institut Paoli Calmettes
  • Maastricht University
  • University Medical Center Hamburg-Eppendorf
  • International Hospital Istanbul
  • Maria Sklodowska-Curie Institute of Oncology
  • American University of Beirut
  • Vanderbilt University
  • Sheba Medical Center at Tel Hashomer

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

In this registry-based study which includes acute myeloid leukemia patients who underwent a matched unrelated donor allogeneic peripheral-blood stem cell transplantation in complete remission and received post-transplant cyclophosphamide (PTCY) as graft-versus-host disease (GvHD) prophylaxis, we compared 421 recipients without anti-thymocyte globulin (ATG) with 151 patients with ATG. The only significant differences between PTCY and PTCY + ATG cohorts were the median year of transplant and the follow-up period (2017 vs 2015 and 19.6 vs 31.1 months, respectively, p < 0.0001). Overall, 2-year survival was 69.9% vs 67.1% in PTCY and PTCY + ATG, respectively, with deaths related to relapse (39% vs 43.5%), infection (21.9% vs 23.9%) or GvHD (17.1% vs 17.4%) not differing between groups. On univariate comparison, a significantly lower rate of extensive chronic GvHD was found when ATG was added (9.9% vs 21%, p = 0.029), a finding which was not confirmed in the multivariate analysis. The Cox-model showed no difference between PTCY + ATG and PTCY alone with respect to acute and chronic GvHD of all grades, non-relapse mortality, relapse, leukemia-free survival, overall survival, and GvHD-free-relapse-free survival between study cohorts. Our results highlight that the addition of ATG in PTCY does not provide any extra benefit in terms of further GvHD reduction, better GRFS or better survival.

Original languageEnglish
Pages (from-to)1774-1780
Number of pages7
JournalBone marrow transplantation
Volume57
Issue number12
Early online date2022
DOIs
Publication statusPublished - Dec 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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