TY - JOUR
T1 - Improved Posttransplant Outcomes in Recent Years for AML Patients with FLT3-ITD and Wild-type NPM1
T2 - A Report from the EBMT Acute Leukemia Working Party
AU - Bazarbachi, Ali
AU - Labopin, Myriam
AU - Gedde-Dahl, Tobias
AU - Remenyi, Peter
AU - Forcade, Edouard
AU - Kröger, Nicolaus
AU - Socié, Gerard
AU - Craddock, Charles
AU - Bourhis, Jean Henri
AU - Versluis, Jurjen
AU - Yakoub-Agha, Ibrahim
AU - Salmenniemi, Urpu
AU - El-Cheikh, Jean
AU - Bug, Gesine
AU - Esteve, Jordi
AU - Nagler, Arnon
AU - Ciceri, Fabio
AU - Mohty, Mohamad
N1 - Publisher Copyright:
©2023 American Association for Cancer Research.
PY - 2023/11/1
Y1 - 2023/11/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85175878206&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-23-0954
DO - 10.1158/1078-0432.CCR-23-0954
M3 - Article
C2 - 37603683
AN - SCOPUS:85175878206
SN - 1078-0432
VL - 29
SP - 4441
EP - 4448
JO - Clinical Cancer Research : an official journal of the American Association for Cancer Research
JF - Clinical Cancer Research : an official journal of the American Association for Cancer Research
IS - 21
ER -