Prognostic value of a new clinically-based classification system in patients with CMML undergoing allogeneic HCT: a retrospective analysis of the EBMT-CMWP

  • Francesco Onida
  • Giulia Sbianchi
  • Aleksandar Radujkovic
  • Katja Sockel
  • Nicolaus Kröger
  • Jorge Sierra
  • Gerard Socié
  • Jan Cornelissen
  • Xavier Poiré
  • Luděk Raida
  • Jean Henri Bourhis
  • Jürgen Finke
  • Jakob Passweg
  • Urpu Salmenniemi
  • Harry C Schouten
  • Yves Beguin
  • Sonja Martin
  • Eric Deconinck
  • Arnold Ganser
  • Samo Zver
  • Bruno Lioure
  • Radia Rohini
  • Linda Koster
  • Patrick Hayden
  • Simona Iacobelli
  • Marie Robin
  • Ibrahim Yakoub-Agha

Abstract

Recently a new three-group clinical classification was reported by an International Consortium to stratify CMML patients with regard to prognosis. The groups were defined as follows: (1) Myelodysplastic (MD)-CMML: WBC ≤ 10 × 109/l, circulating immature myeloid cells (IMC) = 0, no splenomegaly; (2) MD/MP (overlap)-CMML: WBC 10-20 × 109/l or WBC ≤ 10 × 109/l but IMC > 0 and/or splenomegaly; (3) Myeloproliferative (MP)-CMML: WBC > 20 × 109/l. By analysing EBMT Registry patients who underwent allo-HCT for CMML between 1997 and 2016, we aimed to determine the impact of this classification on transplantation outcome and to make a comparison with the conventional WHO classification (CMML-0/CMML-1/CMML-2). Patient grouping was based on the data registered at time of transplantation, with IMC replaced by peripheral blasts. Among 151 patients included in the analysis, 38% were classified as MD-CMML, 42% as MD/MP-CMML and 20% as MP-CMML. With a median survival of 17 months in the whole series, MD-CMML patients were distinguished as a low-risk group with higher CR rate at transplant and a longer post-transplant 2-year progression-free survival in comparison to others (44.5% vs 33.5%, respectively), whereas the WHO classification was superior in identifying high-risk patients (CMML-2) with inferior survival outcomes.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0268-3369
DOIs
StatusVeröffentlicht - 06.2022

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

PubMed 35352038