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The impact of cytogenetic risk on the outcomes of allogeneic hematopoietic cell transplantation in patients with relapsed/refractory acute myeloid leukemia: On behalf of the acute leukemia working party (ALWP) of the European group for blood and marrow transplantation (EBMT)

  • Monica Poiani
  • , Myriam Labopin
  • , Giorgia Battipaglia*
  • , Dietrich W. Beelen
  • , Johanna Tischer
  • , Jürgen Finke
  • , Arne Brecht
  • , Edouard Forcade
  • , Arnold Ganser
  • , Jakob R. Passweg
  • , Helene Labussiere-Wallet
  • , Ibrahim Yakoub-Agha
  • , Kerstin Schäfer-Eckart
  • , Nicolaus Kroeger
  • , Blandine Guffroy
  • , Annalisa Ruggeri
  • , Jordi Esteve
  • , Arnon Nagler
  • , Mohamad Mohty
  • *Corresponding author for this work
  • Sorbonne Université
  • Azienda Ospedaliera Universitaria Ospedali Riuniti di Ancona
  • EBMT Paris Study Office
  • University of Naples Federico II
  • University of Duisburg-Essen
  • Ludwig Maximilian University of Munich
  • University of Freiburg
  • Deutsche Klinik für Diagnostik
  • Hôpital du Haut-Lévêque
  • Hannover Medical School
  • University of Basel
  • Hospices civils de Lyon
  • Université de Lille
  • Klinikum Nurnberg
  • University of Hamburg
  • University Hospital of Strasbourg
  • San Raffaele Scientific Institute
  • Hospital Clinic Barcelona
  • Sheba Medical Center at Tel Hashomer

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Karyotypic analysis at time of diagnosis has an important value in determining initial response to treatment, remission duration and overall survival (OS) in acute myeloid leukemia (AML). Less is known about its value before allogeneic hematopoietic cell transplantation (allo-HCT) in patients transplanted with active disease, either relapsed or primary refractory (Rel-Ref) AML. We explored the impact of cytogenetic risk (stratification according to MRC-UK) in 2089 patients with either Ref (n = 972) or Rel AML (n = 1117) transplanted during the period 2000-2017. Overall, 154 patients had a favorable risk, 1283 had an intermediate risk and 652 had an adverse cytogenetic risk. Median follow-up was 49 months. Compared to the favorable risk group, intermediate and adverse risk patients were associated with worse leukemia-free survival and OS and also with a higher incidence of relapse. In a subgroup analysis of patients in the intermediate risk group harboring Fms-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD), this remained an important prognostic factor, being associated with worse outcomes. When analyzing patients according to the intensity of the conditioning regimen, no differences were observed for the main transplant outcomes. In conclusion, in patients diagnosed with AML and transplanted with active disease, karyotype remains an important prognostic factor, allowing splitting patients into different risk groups according to their cytogenetics. Similarly, FLT3-ITD mutation also remains a negative prognostic factor in this population.

Original languageEnglish
Pages (from-to)40-50
Number of pages11
JournalAmerican Journal of Hematology
Volume96
Issue number1
DOIs
StatePublished - Jan 2021
Externally publishedYes

Funding

Funders
EBMT

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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