Management of adult patients with CMML undergoing allo-HCT: recommendations from the EBMT PH&G Committee

Francesco Onida, Nico Gagelmann, Yves Chalandon, Guido Kobbe, Marie Robin, Argiris Symeonidis, Theo de Witte, Raphael Itzykson, Madlen Jentzsch, Uwe Platzbecker, Valeria Santini, Guillermo Sanz, Christof Scheid, Eric Solary, Peter Valent, Raffaela Greco, Isabel Sanchez-Ortega, Ibrahim Yakoub-Agha, Lisa Pleyer* (Last author)

*Corresponding author for this work

Research output: Contribution to journalOriginal Articlepeer-review

2 Citations (Web of Science)

Abstract

Chronic myelomonocytic leukemia (CMML) is a heterogeneous disease presenting with either myeloproliferative or myelodysplastic features. Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only potentially curative option, but the inherent toxicity of this procedure makes the decision to proceed to allo-HCT challenging, particularly because patients with CMML are mostly older and comorbid. Therefore, the decision between a nonintensive treatment approach and allo-HCT represents a delicate balance, especially because prospective randomized studies are lacking and retrospective data in the literature are con fl icting. International consensus on the selection of patients and the ideal timing of allo-HCT, speci fi cally in CMML, could not be reached in international recommendations published 6 years ago. Since then, new, CMML-speci fi c data have been published. The European Society for Blood and Marrow Transplantation (EBMT) Practice Harmonization and Guidelines (PH&G) Committee assembled a panel of experts in the fi eld to provide the fi rst best practice recommendations on the role of allo-HCT speci fi cally in CMML. Recommendations were based on the results of an international survey, a comprehensive review of the literature, and expert opinions on the subject, after structured discussion and circulation of recommendations. Algorithms for patient selection, timing of allo-HCT during the course of the disease, pretransplant strategies, allo-HCT modality, as well as posttransplant management for patients with CMML were outlined. The keynote message is, that once a patient has been identi fi ed as a transplant candidate, upfront transplantation without prior disease -modifying treatment is preferred to maximize chances of reaching allo-HCT whenever possible, irrespective of bone marrow blast counts.
Original languageEnglish
Pages (from-to)2227-2244
Number of pages18
JournalBLOOD
Volume143
Issue number22
DOIs
Publication statusPublished - 30 May 2024

Keywords

  • Stem-cell transplantation
  • Chronic myelomonocytic leukemia
  • Acute myeloid-leukemia
  • Prognostic scoring system
  • Risk myelodysplastic syndrome
  • Randomized phase-iii
  • Bone-marrow fibrosis
  • Hypomethylating agents
  • Iron overload
  • Free survival

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