Allogeneic haematopoietic cell transplantation for therapy-related myeloid neoplasms arising following treatment for lymphoma: a retrospective study on behalf of the Chronic Malignancies Working Party of the EBMT

  • Mitja Nabergoj
  • Diderik-Jan Eikema
  • Linda Koster
  • Uwe Platzbecker
  • Katja Sockel
  • Jürgen Finke
  • Nicolaus Kröger
  • Edouard Forcade
  • Arnon Nagler
  • Matthias Eder
  • Johanna Tischer
  • Annoek E C Broers
  • Jürgen Kuball
  • Keith M O Wilson
  • Mathilde Hunault-Berger
  • Matthew Collin
  • Domenico Russo
  • Lucía López Corral
  • Grzegorz Helbig
  • Alberto Mussetti
  • Christof Scheid
  • Carmelo Gurnari
  • Kavita Raj
  • Joanna Drozd-Sokolowska
  • Ibrahim Yakoub-Agha
  • Marie Robin
  • Donal P McLornan

Abstract

Therapy-related myeloid neoplasms (t-MN), either myelodysplastic neoplasms (t-MDS) or acute myeloid leukemias (t-AML), have a poor prognosis and allogeneic haematopoietic cell transplantation (allo-HCT) represents the only curative option. In this multicenter, registry-based study, we analyzed outcomes of 378 patients undergoing first allo-HCT between 2006-2017 for t-MN arising secondary to lymphoma treatment. Median age was 58 years at allo-HCT; 222 (59%) had a diagnosis of t-MDS and 156 (41%) of t-AML, respectively. At the time of allo-HCT, 46% of t-MN cases were reported as in complete remission (CR) and 15% of lymphomas were recorded as not in remission. A reduced intensity conditioning regimen was used in 70% of cases. For the entire cohort, 5-year OS, and t-MN PFS, relapse incidence and NRM were 32%, 28%, 35% and 37%, respectively. In multivariable analysis, undergoing allo-HCT with t-MN not in CR and older age were associated with significantly worse OS, PFS and NRM. At 5 years post allo-HCT, the relapse incidence of lymphoma was low at 3%, while the rate of secondary malignancies was 8%. This analysis shows the curative potential of allo-HCT for patients with t-MN arising secondary to lymphoma treatment in approximately a third of patients.

Bibliographical data

Original languageEnglish
ISSN0268-3369
DOIs
Publication statusPublished - 03.2024

Comment Deanary

© 2024. The Author(s), under exclusive licence to Springer Nature Limited.

PubMed 38195984