Salman Huda
Brown Center for Immunotherapy, Melvin and Bren Simon Comprehensive Cancer Center, School of Medicine, Indiana University, Indianapolis, IN 46202, USA.
Cancers (Basel). 2024 Aug 22;16(16):2915. doi: 10.3390/cancers16162915.
Comprehensive analyses of the molecular heterogeneity of acute myelogenous leukemia, AML, particularly when malignant cells retain normal karyotype, has significantly evolved. In 2022, significant revisions were introduced in the World Health Organization (WHO) classification and the European LeukemiaNet (ELN) 2022 guidelines of acute myeloid leukemia (AML). These revisions coincided with the inception of the first version of the International Consensus Classification (ICC) for AML. These modifications aim to improve diagnosis and treatment outcomes via a comprehensive incorporation of sophisticated genetic and clinical parameters as well as facilitate accruals to innovative clinical trials. Key updates include modifications to the blast count criteria for AML diagnosis, with WHO 2022 eliminating the ≥20% blast requirement in the presence of AML-defining abnormalities and ICC 2022 setting a 10% cutoff for recurrent genetic abnormalities. Additionally, new categories, such as AML with mutated TP53 and MDS/AML, were introduced. ELN 2022 guidelines retained risk stratification approach and emphasized the critical role of measurable residual disease (MRD) that increased the use of next-generation sequencing (NGS) and flow cytometry testing. These revisions underscore the importance of precise classification for targeted treatment strategies and improved patient outcomes. How much difference versus concordance these classifications present and the impact of those on clinical practice is a continuing discussion.
对急性髓系白血病(AML)分子异质性的全面分析,尤其是当恶性细胞保持正常核型时,已经有了显著进展。2022年,世界卫生组织(WHO)分类和欧洲白血病网(ELN)2022年急性髓系白血病(AML)指南引入了重大修订。这些修订恰逢AML国际共识分类(ICC)第一版的出台。这些修改旨在通过全面纳入复杂的遗传和临床参数来改善诊断和治疗结果,并促进参与创新临床试验。关键更新包括对AML诊断的原始细胞计数标准的修改,WHO 2022在存在AML定义异常的情况下取消了≥20%原始细胞的要求,而ICC 2022为复发性遗传异常设定了10%的临界值。此外,还引入了新的类别,如伴有TP53突变的AML和MDS/AML。ELN 2022指南保留了风险分层方法,并强调了可测量残留病(MRD)的关键作用,这增加了下一代测序(NGS)和流式细胞术检测的使用。这些修订强调了精确分类对于靶向治疗策略和改善患者预后的重要性。这些分类之间存在多大差异与一致性以及它们对临床实践的影响仍在持续讨论中。