Allogeneic hematopoietic cell transplantation for patients with AML aged 70 years or older in first remission. A study from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation (EBMT)

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Enrico Maffini
  • Maud Ngoya
  • Jacques Emmanuel Galimard
  • Samia Harbi
  • Nicolaus Kröger
  • Uwe Platzbecker
  • Charles Craddock
  • Victoria Potter
  • Goda Choi
  • Patrice Chevallier
  • Friedrich Stölzel
  • Eleni Tholouli
  • Johan Maertens
  • Fabio Ciceri
  • Jan Cornelissen
  • Jaime Sanz
  • Alexandros Spyridonidis
  • Francesco Lanza
  • Arnon Nagler
  • Mohamad Mohty

Accessibility to allogeneic hematopoietic cell transplantation (HCT) programs for older patients is growing constantly. We report on the clinical outcomes of a group of 701 adults aged ≥70 years, with acute myeloid leukemia (AML) in first complete remission (CR1), who received a first HCT, from HLA-matched sibling donors (MSD), 10/10 HLA-matched unrelated donors (UD), 9/10 HLA-mismatched unrelated donors (mUD) or haploidentical (Haplo) donors. The 2-year overall survival (OS) was 48.1%, leukemia-free survival (LFS) 45.3%, relapse incidence (RI) 25.2%, non-relapse mortality (NRM) 29.5% and GVHD-free, relapse-free survival (GRFS), 33.4%. Compared to MSD, patients transplanted from Haplo and UD presented lower RI (HR 0.46, 95% CI 0.25–0.8, p = 0.02 and HR 0.44, 95% CI: 0.28–0.69, p = 0.001, respectively); this translated into prolonged LFS for Haplo (HR 0.62, 95% CI: 0.39–0.99, p = 0.04). Patients transplanted from mUD exhibited the highest NRM incidence (HR 2.33, 95% CI: 1.26–4.31, p = 0.007). HCT in selected adult CR1 AML patients >70 years is feasible and could be associated with good clinical outcomes. Prospective clinical trials are warranted.

OriginalsprogEngelsk
TidsskriftBone Marrow Transplantation
Vol/bind58
Udgave nummer9
Sider (fra-til)1033-1041
Antal sider9
ISSN0268-3369
DOI
StatusUdgivet - 2023

Bibliografisk note

Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.

ID: 397720734