Allogeneic hematopoietic cell transplantation in patients with myelodysplastic syndrome using treosulfan based compared to other reduced-intensity or myeloablative conditioning regimens. A report of the chronic malignancies working party of the EBMT

  • Avichai Shimoni
  • Marie Robin
  • Simona Iacobelli
  • Dietrich Beelen
  • Ghulam J Mufti
  • Fabio Ciceri
  • Wolfgang Bethge
  • Liisa Volin
  • Didier Blaise
  • Arnold Ganser
  • Thomas Luft
  • Patrice Chevallier
  • Rainer Schwerdtfeger
  • Linda Koster
  • Theo de Witte
  • Nicolaus Kröger
  • Arnon Nagler
  • Ibrahim Yakoub-Agha

Abstract

Allogeneic haematopoietic-cell transplantation (allo-HCT) is a potentially curative therapy for high-risk myelodysplastic syndrome (MDS). Reduced-intensity conditioning (RIC) is usually associated with lower non-relapse mortality (NRM), higher relapse rate and similar overall-survival (OS) as myeloablative-conditioning (MAC). Fludarabine/treosulfan (FT) is a reduced-toxicity regimen with intense anti-leukaemia activity and a favourable toxicity profile. We investigated post-transplant outcomes in 1722 MDS patients following allo-HCT with FT (n = 367), RIC (n = 687) or MAC (n = 668). FT and RIC recipients were older than MAC recipients, median age 59, 59 and 51 years, respectively (P < 0·001) but other disease characteristics were similar. The median follow-up was 64 months (1-171). Five-year relapse rates were 25% (21-30), 38% (34-42) and 25% (22-29), after FT, RIC and MAC, respectively, (P < 0·001). NRM was 30% (25-35), 27% (23-30) and 34% (31-38, P = 0·008), respectively. Five-year OS was 50% (44-55), 43% (38-47), and 43% (39-47), respectively (P = 0·03). In multivariate analysis, FT was associated with a lower risk of relapse (HR 0·55, P < 0·001) and better OS (HR 0·72, P = 0·01). MAC was associated with higher NRM (HR 1·44, P = 0·001). In conclusion, FT is associated with similar low relapse rates as MAC and similar low NRM as RIC, resulting in improved OS. FT may be the preferred regimen for allo-HCT in MDS.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0007-1048
DOIs
StatusVeröffentlicht - 11.2021

Anmerkungen des Dekanats

© 2021 British Society for Haematology and John Wiley & Sons Ltd.

PubMed 34514596