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Comparative value of post-remission treatment in cytogenetically normal AML subclassified by NPM1 and FLT3-ITD allelic ratio

  • J. Versluis
  • , F. E. M. In 't Hout
  • , R. Devillier
  • , W. L. J. van Putten
  • , M. G. Manz
  • , M.-C. Vekemans
  • , M.-C. Legdeur
  • , J. R. Passweg
  • , J. Maertens
  • , J. Kuball
  • , B. J. Biemond
  • , P. J. M. Valk
  • , B. A. van der Reijden
  • , G. Meloni
  • , H. C. Schouten
  • , E. Vellenga
  • , T. Pabst
  • , R. Willemze
  • , B. Löwenberg
  • , G. Ossenkoppele
  • F. Baron, G. Huls, J. J. Cornelissen
  • Erasmus Medical Center
  • Radboud University Medical Center
  • University of Zurich
  • Hôpital St Luc
  • Medisch Spectrum Twente (MST)
  • University Hospital Basel
  • University Hospital Gasthuisberg
  • University Medical Center Utrecht
  • Academic Medical Center
  • University of Rome La Sapienza
  • Maastricht UMC
  • University Medical Center Groningen
  • Bern University Hospital ‘Inselspital’
  • Leiden University Medical Center
  • University of Liege

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Post-remission treatment (PRT) in patients with cytogenetically normal (CN) acute myeloid leukemia (AML) in first complete remission (CR1) is debated. We studied 521 patients with CN-AML in CR1, for whom mutational status of NPM1 and FLT3-ITD was available, including the FLT3-ITD allelic ratio. PRT consisted of reduced intensity conditioning (RIC) allogeneic hematopoietic stem cell transplantation (alloHSCT) (n = 68), myeloablative conditioning (MAC) alloHSCT (n = 137), autologous hematopoietic stem cell transplantation (autoHSCT) (n = 168) or chemotherapy (n = 148). Favorable overall survival (OS) was found for patients with mutated NPM1 without FLT3-ITD (71 +/- 4%). Outcome in patients with a high FLT3-ITD allelic ratio appeared to be very poor with OS and relapse-free survival (RFS) of 23 +/- 8% and 12 +/- 6%, respectively. Patients with wild-type NPM1 without FLT3-ITD or with a low allelic burden of FLT3-ITD were considered as intermediate-risk group because of similar OS and RFS at 5 years, in which PRT by RIC alloHSCT resulted in better OS and RFS as compared with chemotherapy (hazard ratio (HR) 0.56, P = 0.022 and HR 0.50, P = 0.004, respectively) or autoHSCT (HR 0.60, P = 0.046 and HR 0.60, P = 0.043, respectively). The lowest cumulative incidence of relapse (23 +/- 4%) was observed following MAC alloHSCT. These results suggest that alloHSCT may be preferred in patients with molecularly intermediate-risk CN-AML, while the choice of conditioning type may be personalized according to risk for non-relapse mortality
Original languageEnglish
Pages (from-to)26-33
Number of pages8
JournalLeukemia
Volume31
Issue number1
Early online date2016
DOIs
Publication statusPublished - 1 Jan 2017

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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