Outcomes following second allogeneic haematopoietic cell transplantation in patients with myelofibrosis: a retrospective study of the Chronic Malignancies Working Party of EBMT

  • Mitja Nabergoj
  • Katya Mauff
  • Marie Robin
  • Nicolaus Kröger
  • Emanuele Angelucci
  • Xavier Poiré
  • Jakob Passweg
  • Aleksandar Radujkovic
  • Uwe Platzbecker
  • Stephen Robinson
  • Alessandro Rambaldi
  • Søren Lykke Petersen
  • Fridrich Stölzel
  • Matthias Stelljes
  • Fabio Ciceri
  • Jiri Mayer
  • Marco Ladetto
  • Liesebeth C de Wreede
  • Linda Koster
  • Patrick J Hayden
  • Tomasz Czerw
  • Juan Carlos Hernández-Boluda
  • Donal McLornan
  • Yves Chalandon
  • Ibrahim Yakoub-Agha

Abstract

Therapeutic management of patients with primary or secondary myelofibrosis (MF) who experience relapse or graft failure following allogeneic haematopoietic cell transplantation (allo-HCT) remains heterogeneous. We retrospectively analyzed 216 patients undergoing a second allo-HCT for either relapse (56%) or graft failure (31%) between 2010 and 2017. Median age was 57.3 years (range 51-63). The same donor as for the first allo-HCT was chosen in 66 patients (31%) of whom 19 received an HLA-identical sibling donor, whereas a different donor was chosen for 116 patients (54%). Median follow-up was 40 months. Three-year overall survival (OS) and relapse-free survival (RFS) were 42% and 39%, respectively. Three-year non-relapse mortality (NRM) and relapse rates were 36% and 25%, respectively. Grade II-IV and III-IV acute GVHD occurred in 25% and 11% of patients, respectively, and the 3-year incidence of chronic GVHD was 33% including 14% for extensive grade. Graft-failure incidence at 1 year was 14%. In conclusion, our data suggest that a second allo-HCT is a potential option for patients failing first allo-HCT for MF albeit careful patient assessment is fundamental to identify individual patients who could benefit from this approach.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0268-3369
DOIs
StatusVeröffentlicht - 08.2021

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© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

PubMed 33824436