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Post-transplant cyclophosphamide separates graft-versus host disease and graft versus leukemia effects after HLA-matched stem-cell transplantation for acute myeloid leukemia

  • Avichai Shimoni*
  • , Christophe Peczynski
  • , Myriam Labopin
  • , Alexander Kulagin
  • , Ellen Meijer
  • , Jan Cornelissen
  • , Goda Choi
  • , Jaime Sanz
  • , Montserrat Rovira
  • , Gwendolyn van Gorkom
  • , Nicolaus Kröger
  • , Yener Koc
  • , Jan Vydra
  • , J. L. Diez-Martin
  • , Carlos Solano
  • , Amit Patel
  • , Patrizia Chiusolo
  • , Fabio Ciceri
  • , Arnon Nagler
  • , Mohamad Mohty
  • *Corresponding author for this work
  • Tel Aviv University
  • Sorbonne Université
  • Pavlov University
  • Erasmus University Rotterdam
  • University of Groningen
  • Hospital Universitario La Fe
  • Hospital Clinic de Barcelona
  • Maastricht University
  • University of Hamburg
  • International Hospital Istanbul
  • Institute of Hematology and Blood Transfusion
  • Hospital General Universitario Gregorio Marañon
  • Hospital Clinico Universitario de Valencia
  • Liverpool University Hospitals NHS Foundation Trust
  • Catholic University of the Sacred Heart
  • IRCCS Ospedale San Raffaele

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

The association of graft-versus-host disease (GVHD) and graft-versus-leukemia (GVL) effects after allogeneic stem-cell transplantation (SCT) is well-established but was not confirmed in the modern era and following post-transplant cyclophosphamide (PTCy). We assessed GVHD/ GVL association in AML patients following HLA-matched SCT with standard calcineurin-based (n = 12,653, 57% with additional in-vivo T-cell depletion) or PTCy-based (n = 508) GVHD prophylaxis. Following standard prophylaxis, acute GVHD grade II-IV and III-IV, chronic GVHD, and extensive chronic GVHD rates were 23.8%, 7.5%, 37.0%, and 16.3%, respectively. Acute GVHD grade II and III-IV were associated with lower relapse [hazard-ratio (HR) 0.85, P = 0.002; HR 0.76, P = 0.003, respectively)], higher non-relapse mortality (NRM) (HR 1.5, P < 0.001; HR 6.21, P < 0.001) and lower overall survival (OS) (HR 1.49, P < 0.001; HR 6.1, P < 0.001). Extensive chronic GVHD predicted lower relapse (HR 0.69, P < 0.001), higher NRM (HR 2.83, P < 0.001), and lower OS (HR 2.74, P < 0.001). Following PTCy, GVHD rates were 22.8%, 6.2%, 35.5%, and 17.7%, respectively. Acute GVHD was not associated with relapse (HR 1.37, P = 0.15) but predicted higher NRM (HR 3.34, P < 0.001) and lower OS (HR 1.92, P = 0.001). Chronic GVHD was not prognostic for these outcomes. In conclusion, GVHD and GVL are strongly associated with contemporary SCT. However, following PTCy, GVHD is not associated with reduced relapse.

Original languageEnglish
JournalLeukemia
Early online date2024
DOIs
Publication statusE-pub ahead of print - 2024

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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