Contributions of ELN2022 update and new genetic analysis tests in the risk assesment and treatment of acute myeloid leukaemia

Seda Yilmaz, M. Bağcı, Abdulkadir Baştürk
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Abstract

Acute myeloid leukaemia (AML) is a heterogeneous disease including cytogenetic and molecular abnormalities. Age, performance status and specific genetic characteristics are important in prognosis. Both directing consolidation treatment and having genetic-based treatment targets have made genetic results even more important. The European LeukemiaNet (ELN) 2022 report was published by expanding the genetic mutation profile. In order to question what this update has changed in clinical practice, we reviewed the data of patients with acute myeloid leukaemia in whom myeloid panel was studied by Next-Generation Sequencing (NGS).
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ELN2022 更新版和新基因分析测试对急性髓性白血病风险评估和治疗的贡献
急性髓性白血病(AML)是一种异质性疾病,包括细胞遗传学和分子异常。年龄、表现状态和特定的遗传特征对预后非常重要。指导巩固治疗和基于基因的治疗目标都使基因结果变得更加重要。欧洲白血病网络(ELN)2022 年报告的发布扩大了基因突变的范围。为了探究这一更新对临床实践有何改变,我们回顾了通过下一代测序(NGS)研究了髓样板的急性髓性白血病患者的数据。
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