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Continuously improving outcome over time after second allogeneic stem cell transplantation in relapsed acute myeloid leukemia: an EBMT registry analysis of 1540 patients.

Authors :
Schmälter, Ann-Kristin
Ngoya, Maud
Galimard, Jacques-Emmanuel
Bazarbachi, Ali
Finke, Jürgen
Kröger, Nicolaus
Bornhäuser, Martin
Stelljes, Matthias
Stölzel, Friedrich
Tischer, Johanna
Schroeder, Thomas
Dreger, Peter
Blau, Igor-Wolfgang
Savani, Bipin
Giebel, Sebastian
Esteve, Jordi
Nagler, Arnon
Schmid, Christoph
Ciceri, Fabio
Mohty, Mohamad
Source :
Blood Cancer Journal; 5/2/2024, Vol. 14 Issue 1, p1-8, 8p
Publication Year :
2024

Abstract

Second allogeneic stem cell transplantation (alloSCT2) is among the most effective treatments for acute myeloid leukemia (AML) relapse after first alloSCT (alloSCT1). Long-term EBMT registry data were used to provide large scale, up-to-date outcome results and to identify factors for improved outcome. Among 1540 recipients of alloSCT2, increasing age, better disease control and performance status before alloSCT2, more use of alternative donors and higher conditioning intensity represented important trends over time. Between the first (2000–2004) and last (2015–2019) period, two-year overall and leukemia-free survival (OS/LFS) increased considerably (OS: 22.5–35%, LFS: 14.5–24.5%). Cumulative relapse incidence (RI) decreased from 64% to 50.7%, whereas graft-versus-host disease and non-relapse mortality (NRM) remained unchanged. In multivariable analysis, later period of alloSCT2 was associated with improved OS/LFS (HR = 0.47/0.53) and reduced RI (HR = 0.44). Beyond, remission duration, disease stage and patient performance score were factors for OS, LFS, RI, and NRM. Myeloablative conditioning for alloSCT2 decreased RI without increasing NRM, leading to improved OS/LFS. Haploidentical or unrelated donors and older age were associated with higher NRM and inferior OS. In summary, outcome after alloSCT2 has continuously improved over the last two decades despite increasing patient age. The identified factors provide clues for the optimized implementation of alloSCT2. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20445385
Volume :
14
Issue :
1
Database :
Complementary Index
Journal :
Blood Cancer Journal
Publication Type :
Academic Journal
Accession number :
177044573
Full Text :
https://doi.org/10.1038/s41408-024-01060-4