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

IF 5.1 2区 医学 Q1 HEMATOLOGY British Journal of Haematology Pub Date : 2024-05-29 DOI:10.1111/bjh.19518
Carlos Jiménez-Vicente, Paola Charry, Sandra Castaño-Diez, Francesca Guijarro, Mònica López-Guerra, Amanda Isabel Pérez-Valencia, Alexandra Martinez-Roca, Albert Cortés-Bullich, Daniel Munárriz, Maria Teresa Solano, Laura Rosiñol, Enric Carreras, Álvaro Urbano-Ispizua, Francesc Fernández-Avilés, Carmen Martinez, María Suárez-Lledó, Marina Díaz-Beyá, Montserrat Rovira, María Queralt Salas, Jordi Esteve
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Abstract

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.

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对接受异基因造血干细胞移植治疗急性髓性白血病患者的欧洲白血病网络 2022 风险分类进行评估:确定预后极差的基因组。
欧洲白血病网络(European LeukemiaNet)根据同年公布的两个新的髓系白血病分类,对2022年急性髓系白血病(AML)的风险分类(ELN 2022)进行了改进。我们对本中心2011年至2021年接受异基因造血细胞移植(allo-HCT)的120名急性髓性白血病患者(包括99名首次完全反应(CR1)患者)进行了回顾性评估,以确定ELN 2022的预后价值。不良风险患者(Adv)在总生存期(OS)和无白血病生存期(LFS)方面表现较差(OS [p = 0.003],LFS [p = 0.02]),多变量分析证实了这一点(OS 的危险比 [HR] = 2.00,p = 0.037)。这些结果也出现在 CR1 异体移植的患者中。进一步分析发现,包括复杂核型、MECOM(EVI1)重排和TP53突变在内的一个名为adverse-plus (AdvP)的亚组,其预后比包括Adv在内的其他患者组更差(OS的危险比[HR]=3.14,p=0.037):3.14, p
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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