Department of Epidemiology & Biostatistics, Computational Oncology Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Memorial Sloan Kettering Kids, Memorial Sloan Kettering Cancer Center, New York, NY.
Blood Adv. 2023 Sep 12;7(17):5000-5013. doi: 10.1182/bloodadvances.2023009675.
Accurate classification and risk stratification are critical for clinical decision making in patients with acute myeloid leukemia (AML). In the newly proposed World Health Organization and International Consensus classifications of hematolymphoid neoplasms, the presence of myelodysplasia-related (MR) gene mutations is included as 1 of the diagnostic criteria for AML, AML-MR, based largely on the assumption that these mutations are specific for AML with an antecedent myelodysplastic syndrome. ICC also prioritizes MR gene mutations over ontogeny (as defined in the clinical history). Furthermore, European LeukemiaNet (ELN) 2022 stratifies these MR gene mutations into the adverse-risk group. By thoroughly annotating a cohort of 344 newly diagnosed patients with AML treated at the Memorial Sloan Kettering Cancer Center, we show that ontogeny assignments based on the database registry lack accuracy. MR gene mutations are frequently observed in de novo AML. Among the MR gene mutations, only EZH2 and SF3B1 were associated with an inferior outcome in the univariate analysis. In a multivariate analysis, AML ontogeny had independent prognostic values even after adjusting for age, treatment, allo-transplant and genomic classes or ELN risks. Ontogeny also helped stratify the outcome of AML with MR gene mutations. Finally, de novo AML with MR gene mutations did not show an adverse outcome. In summary, our study emphasizes the importance of accurate ontogeny designation in clinical studies, demonstrates the independent prognostic value of AML ontogeny, and questions the current classification and risk stratification of AML with MR gene mutations.
准确的分类和风险分层对于急性髓系白血病(AML)患者的临床决策至关重要。在新提出的世界卫生组织和国际血液淋巴肿瘤共识分类中,存在骨髓增生异常相关(MR)基因突变被纳入 AML、AML-MR 的诊断标准之一,主要基于这些突变是 AML 伴先前骨髓增生异常综合征的特异性假设。国际癌症控制联盟(ICC)还优先考虑 MR 基因突变而不是个体发生(在临床病史中定义)。此外,欧洲白血病网络(ELN)2022 将这些 MR 基因突变分为不良风险组。通过对在纪念斯隆凯特琳癌症中心治疗的 344 例新诊断 AML 患者进行全面注释,我们表明基于数据库注册的个体发生分配缺乏准确性。MR 基因突变在初发性 AML 中经常观察到。在 MR 基因突变中,只有 EZH2 和 SF3B1 在单因素分析中与较差的预后相关。在多因素分析中,即使在调整年龄、治疗、同种异体移植和基因组分类或 ELN 风险后,AML 个体发生也具有独立的预后价值。个体发生也有助于分层具有 MR 基因突变的 AML 的预后。最后,具有 MR 基因突变的初发性 AML 并未显示出不良预后。总之,我们的研究强调了在临床研究中准确指定个体发生的重要性,证明了 AML 个体发生的独立预后价值,并对具有 MR 基因突变的 AML 的当前分类和风险分层提出了质疑。