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基于机器学习的欧洲白血病网 2022 标准和基因组聚类在老年急性髓系白血病中的预后价值。

Prognostic value of European LeukemiaNet 2022 criteria and genomic clusters using machine learning in older adults with acute myeloid leukemia.

机构信息

Department of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea; Leukemia Research Institute, College of Medicine, The Catholic University of Korea, Seoul, Korea; Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.

Department of Hematology, Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea; Leukemia Research Institute, College of Medicine, The Catholic University of Korea, Seoul.

出版信息

Haematologica. 2024 Apr 1;109(4):1095-1106. doi: 10.3324/haematol.2023.283606.

Abstract

This study aimed to validate the new European Leukemia Net (ELN) 2022 criteria for genetic risk stratification in older adults with acute myeloid leukemia (AML) and to determine the most likely set of clusters of similar cytogenetic and mutation properties correlated with survival outcomes in three treatment groups: intensive chemotherapy (IC), hypomethylating agents (HMA) alone, and HMA plus venetoclax (HMA/VEN). The study included 279 patients (aged ≥60 years) who received IC (N=131), HMA (N=76), and HMA/VEN (N=72) between July 2017 and October 2021. No significant differences were observed in survival among the groups according to ELN 2022 risk stratification. Unsupervised hierarchical clustering analysis identified nine genomic clusters (C1-9) with varying survival outcomes depending on treatment type. For example, C4 (predominant for core binding factor-AML) displayed a favorable prognosis in the IC group, but not in the HMA or HMA/VEN groups. The HMA/VEN group had better outcomes than the HMA group in many clusters (C1, 2, 3, and 5); however, the addition of VEN to HMA or IC did not improve the survival outcomes compared with those of HMA alone in C7 and C9 (predominant for -5, del(5q), -7, -17/abn(17p), complex karyotypes, and mutated TP53). The study highlights the limitations of ELN genetic risk stratification in older adults with AML. It emphasizes the need for a more comprehensive approach that considers co-occurring somatic mutations to guide treatment selection in older adults with AML.

摘要

这项研究旨在验证新的欧洲白血病网络(ELN)2022 年用于老年急性髓系白血病(AML)遗传风险分层的标准,并确定与三组治疗相关的最有可能的相似细胞遗传学和突变特征聚类,这三组治疗分别为强化化疗(IC)、单独低甲基化剂(HMA)和 HMA 联合 venetoclax(HMA/VEN)。该研究纳入了 279 名(年龄≥60 岁)在 2017 年 7 月至 2021 年 10 月期间接受 IC(n=131)、HMA(n=76)和 HMA/VEN(n=72)治疗的患者。根据 ELN 2022 年风险分层,各组的生存无显著差异。非监督层次聚类分析确定了九个基因组聚类(C1-9),它们的生存结果因治疗类型而异。例如,C4(主要为核心结合因子-AML)在 IC 组中预后良好,但在 HMA 或 HMA/VEN 组中并非如此。HMA/VEN 组在许多聚类(C1、2、3 和 5)中的结果优于 HMA 组;然而,与 HMA 单独治疗相比,在 C7 和 C9(主要为-5、del(5q)、-7、-17/abn(17p)、复杂核型和突变 TP53)中,将 VEN 添加到 HMA 或 IC 并不能改善生存结果。该研究强调了 ELN 遗传风险分层在老年 AML 患者中的局限性。它强调需要一种更全面的方法,考虑同时发生的体细胞突变,以指导老年 AML 患者的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f0/10985444/3040087837ce/1091095.fig1.jpg

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