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

Author:

Jiménez‐Vicente Carlos12ORCID,Charry Paola3,Castaño‐Diez Sandra12,Guijarro Francesca24,López‐Guerra Mònica235,Pérez‐Valencia Amanda Isabel12,Martinez‐Roca Alexandra12,Cortés‐Bullich Albert12,Munárriz Daniel1,Solano Maria Teresa1,Rosiñol Laura12ORCID,Carreras Enric6,Urbano‐Ispizua Álvaro126,Fernández‐Avilés Francesc126,Martinez Carmen12ORCID,Suárez‐Lledó María12,Díaz‐Beyá Marina12ORCID,Rovira Montserrat126,Salas María Queralt12,Esteve Jordi1267ORCID

Affiliation:

1. Hematology Department Hospital Clínic de Barcelona Barcelona Spain

2. Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) Barcelona Spain

3. Apheresis and Cellular Therapy Unit, Hemotherapy and Hemostasis Department Hospital Clínic de Barcelona Barcelona Spain

4. Hemopathology Unit, Pathology Department Hospital Clinic de Barcelona Barcelona Spain

5. Centro de Investigación Biomédica en Red de Cáncer (CIBERONC) Madrid Spain

6. University of Barcelona Barcelona Spain

7. Josep Carreras Leukemia Research Institute Barcelona Spain

Abstract

SummaryEuropean 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.

Funder

Instituto de Salud Carlos III

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3