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Busulfan-fludarabine versus busulfan-cyclophosphamide for allogeneic transplant in acute myeloid leukemia: long term analysis of GITMO AML-R2 trial

Authors :
Gianluca Cavallaro
Anna Grassi
Chiara Pavoni
Maria Caterina Micò
Alessandro Busca
Irene Maria Cavattoni
Stella Santarone
Carlo Borghero
Attilio Olivieri
Giuseppe Milone
Patrizia Chiusolo
Pellegrino Musto
Riccardo Saccardi
Francesca Patriarca
Fabrizio Pane
Giorgia Saporiti
Paolo Rivela
Elisabetta Terruzzi
Raffaella Cerretti
Giuseppe Marotta
Angelo Michele Carella
Arnon Nagler
Domenico Russo
Paolo Corradini
Paolo Bernasconi
Anna Paola Iori
Luca Castagna
Nicola Mordini
Elena Oldani
Carmen Di Grazia
Andrea Bacigalupo
Alessandro Rambaldi
Source :
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-7 (2024)
Publication Year :
2024
Publisher :
Nature Publishing Group, 2024.

Abstract

Abstract We report the long-term results of a randomized trial (GITMO, AML-R2), comparing 1:1 the combination of busulfan and cyclophosphamide (BuCy2, n = 125) and the combination of busulfan and fludarabine (BuFlu, n = 127) as conditioning regimen in acute myeloid leukemia patients (median age 51 years, range 40–65) undergoing allogeneic hematopoietic stem cell transplantation. With a median follow-up of 6 years, significantly better non-relapse mortality (NRM) was confirmed in BuFlu recipients, which is sustained up to 4 years after transplant (10% vs. 20%, p = 0.0388). This difference was higher in patients older than 51 years (11% in BuFlu vs. 27% in BuCy2, p = 0.0262). The cumulative incidence of relapse, which was the first cause of death in the entire study population, did not differ between the two randomized arms. Similarly, the leukemia-free survival (LFS) and overall survival (OS) were not different in the two cohorts, even when stratifying patients per median age. Graft-and relapse-free survival (GRFS) in BuFlu arm vs. the BuCy2 arm was 25% vs. 20% at 4 years and 20% vs. 17% at 10 years. Hence, the benefit gained by NRM reduction is not offsets by an increased relapse. Leukemia relapse remains a major concern, urging the development of new therapeutic approaches.

Details

Language :
English
ISSN :
20445385
Volume :
14
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Blood Cancer Journal
Publication Type :
Academic Journal
Accession number :
edsdoj.3d88f978b9834d21ac204c0a720eb318
Document Type :
article
Full Text :
https://doi.org/10.1038/s41408-024-01116-5