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Improved Posttransplant Outcomes in Recent Years for AML Patients with FLT3-ITD and Wild-type NPM1: A Report from the EBMT Acute Leukemia Working Party

  • Ali Bazarbachi*
  • , Myriam Labopin
  • , Tobias Gedde-Dahl
  • , Peter Remenyi
  • , Edouard Forcade
  • , Nicolaus Kröger
  • , Gerard Socié
  • , Charles Craddock
  • , Jean Henri Bourhis
  • , Jurjen Versluis
  • , Ibrahim Yakoub-Agha
  • , Urpu Salmenniemi
  • , Jean El-Cheikh
  • , Gesine Bug
  • , Jordi Esteve
  • , Arnon Nagler
  • , Fabio Ciceri
  • , Mohamad Mohty
  • *Corresponding author for this work
  • American University of Beirut
  • Hôpital Saint-Antoine
  • University of Oslo
  • Department of Haematology and Stem Cell Transplant
  • University Hospital of Bordeaux
  • University Medical Center Hamburg-Eppendorf
  • Hospital St. Louis
  • University Hospitals Birmingham NHS Foundation Trust
  • Institut Gustave Roussy
  • Université de Lille
  • Helsinki University Central Hospital
  • University Hospital
  • Hospital Clinic de Barcelona
  • Sheba Medical Center at Tel Hashomer
  • Vita-Salute San Raffaele University

Research output: Contribution to journalArticleAcademicpeer-review

7 Citations (Scopus)

Abstract

PURPOSE: Allogeneic hematopoietic cell transplantation (allo-HCT) is recommended in first complete remission (CR1) in patients with acute myeloid leukemia (AML) harboring FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD). We assessed changes over time in transplant characteristics and outcomes in patients with AML age 60 years and younger with a FLT3-ITD. EXPERIMENTAL DESIGN: We identified 1,827 adult patients with AML (median age 49 years, range 18-60) with FLT3-ITD and intermediate karyotype, allografted between 2012 and 2021 in CR1. RESULTS: NPM1 was mutated in 72% of patients. We compared changes over time in 688 patients transplanted between 2012 and 2016, and 1,139 patients transplanted between 2017 and 2021. For patients with wild-type NPM1, the 2-year leukemia-free survival (LFS) and overall survival (OS) significantly improved over time from 54% to 64% (HR = 0.67; P = 0.011) and from 63% to 71% (HR = 0.66; P = 0.021), respectively. Allo-HCT in recent years significantly reduced the cumulative incidence of relapse (CIR). For patients with NPM1 mutation, no significant changes over time were noted. CONCLUSIONS: In patients with AML with FLT3-ITD and wild-type NPM1, we noticed a significant decrease over time in the CIR and improvement of LFS and OS, likely reflecting the efficacy of FLT-3 inhibitors, including when used as posttransplant maintenance, in this high-risk setting. On the contrary, no significant change over time was noticed in outcomes of patients harboring a FLT3 and NPM1 mutation.

Original languageEnglish
Pages (from-to)4441-4448
Number of pages8
JournalClinical Cancer Research : an official journal of the American Association for Cancer Research
Volume29
Issue number21
DOIs
Publication statusPublished - 1 Nov 2023

Bibliographical note

Publisher Copyright:
©2023 American Association for Cancer Research.

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