Allogeneic stem cell transplantation for AML patients with RUNX1 mutation in first complete remission: a study on behalf of the acute leukemia working party of the EBMT

被引:0
作者
Johanna Waidhauser
Myriam Labopin
Jordi Esteve
Nicolaus Kröger
Jan Cornelissen
Tobias Gedde-Dahl
Gwendolyn Van Gorkom
Jürgen Finke
Montserrat Rovira
Nicolaas Schaap
Eefke Petersen
Dietrich Beelen
Donald Bunjes
Bipin Savani
Christoph Schmid
Arnon Nagler
Mohamad Mohty
机构
[1] Department of Hematology and Medical Oncology,Institute of Hematology and Oncology
[2] University Medical Center Augsburg,undefined
[3] EBMT Paris Study Office,undefined
[4] Saint Antoine Hospital,undefined
[5] INSERM UMR 938,undefined
[6] Sorbonne University,undefined
[7] Hospital Clinic Barcelona,undefined
[8] Bone Marrow Transplantation Centre,undefined
[9] University Hospital Eppendorf,undefined
[10] Department of Hematology,undefined
[11] University Medical Center Rotterdam,undefined
[12] Clinic for Cancer Medicine,undefined
[13] Oslo University Hospital,undefined
[14] Rikshospitalet,undefined
[15] Department of Internal Med. Hematology /Oncology,undefined
[16] University Hospital Maastricht,undefined
[17] Department of Hematology and Medical Oncology,undefined
[18] University of Freiburg,undefined
[19] Department of Hematology,undefined
[20] Nijmegen Medical Centre,undefined
[21] Department of Hematology,undefined
[22] University Medical Centre Utrecht,undefined
[23] Department of Bone Marrow Transplantation,undefined
[24] University Hospital Essen,undefined
[25] Klinik fuer Innere Medizin III,undefined
[26] University Hospital Ulm,undefined
[27] Vanderbilt University Medical Center,undefined
[28] Tel Aviv University,undefined
[29] BMT and Cord Blood Bank,undefined
[30] Chaim Sheba Medical Center,undefined
[31] Department of Hematology,undefined
[32] Saint Antoine Hospital,undefined
来源
Bone Marrow Transplantation | 2021年 / 56卷
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摘要
Acute myeloid leukemia with runt-related transcription factor 1 gene mutation (RUNX1+ AML) is associated with inferior response rates and outcome after conventional chemotherapy. We performed a retrospective, registry-based analysis to elucidate the prognostic value of RUNX1 mutation after allogeneic stem cell transplantation (alloSCT). All consecutive adults undergoing alloSCT for AML in first complete remission (CR1) between 2013 and 2019 with complete information on conventional cytogenetics and RUNX1 mutational status were included. Endpoints of interest were cumulative relapse incidence, non-relapse mortality, overall and leukemia-free survival (OS/LFS), and GvHD-free/relapse-free survival. A total of 674 patients (183 RUNX1+, 491 RUNX1−) were identified, with >85% presenting as de novo AML. Median follow-up was 16.4 (RUNX1+) and 21.9 (RUNX1−) months. Survival rates showed no difference between RUNX1+ and RUNX1− patients either in univariate or multivariate analysis (2-year OS: 67.7 vs. 66.1%, p = 0.7; 2-year LFS: 61.1 vs. 60.8%, p = 0.62). Multivariate analysis identified age, donor type and poor cytogenetics as risk factors for inferior outcome. Among patients with RUNX+ AML, older age, reduced intensity conditioning and minimal residual disease at alloSCT predicted inferior outcome. Our data provide evidence that the negative influence of RUNX1 mutations in patients with AML can be overcome by transplantation in CR1.
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页码:2445 / 2453
页数:8
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