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Evaluation of European LeukemiaNet 2022 risk classification in patients undergoing allogeneic haematopoietic stem cell transplantation for acute myeloid leukaemia: Identification of a very poor prognosis genetic group.

Authors :
Jiménez‐Vicente, Carlos
Charry, Paola
Castaño‐Diez, Sandra
Guijarro, Francesca
López‐Guerra, Mònica
Pérez‐Valencia, Amanda Isabel
Martinez‐Roca, Alexandra
Cortés‐Bullich, Albert
Munárriz, Daniel
Solano, Maria Teresa
Rosiñol, Laura
Carreras, Enric
Urbano‐Ispizua, Álvaro
Fernández‐Avilés, Francesc
Martinez, Carmen
Suárez‐Lledó, María
Díaz‐Beyá, Marina
Rovira, Montserrat
Salas, María Queralt
Esteve, Jordi
Source :
British Journal of Haematology; Jul2024, Vol. 205 Issue 1, p256-267, 12p
Publication Year :
2024

Abstract

Summary: European LeukemiaNet refined their risk classification of acute myeloid leukaemia (AML) in 2022 (ELN 2022) according to the two new myeloid classifications published the same year. We have retrospectively assessed the prognostic value of the ELN 2022 in 120 AML patients undergoing allogeneic haematopoietic cell transplantation (allo‐HCT), including 99 in first complete response (CR1) from 2011 to 2021 in our centre. Adverse risk patients (Adv) presented inferior outcome in terms of overall survival (OS) and leukaemia‐free survival (LFS) (OS [p = 0.003], LFS [p = 0.02]), confirmed in multivariate analysis (hazard ratio [HR] for OS = 2.00, p = 0.037). These results were also seen in patients allografted in CR1. Further analysis identified a subgroup named adverse‐plus (AdvP), including complex karyotype, MECOM(EVI1) rearrangements and TP53 mutations, with worse outcomes than the rest of groups of patients, including the Adv (HR for OS: 3.14, p < 0.001, HR for LFS: 3.36, p < 0.001), with higher 2‐year cumulative incidence of relapse (p < 0.001). Notably, within this analysis, the outcome of Adv and intermediate patients were similar. These findings highlight the prognostic value of ELN 2022 in patients undergoing allo‐HCT, which can be improved by the recognition of a poor genetic subset (AdvP) within the Adv risk group. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00071048
Volume :
205
Issue :
1
Database :
Complementary Index
Journal :
British Journal of Haematology
Publication Type :
Academic Journal
Accession number :
178426601
Full Text :
https://doi.org/10.1111/bjh.19518