Kim Hyunwoo, Lee Ja Young, Yu Shinae, Yoo Eunkyoung, Kim Hye Ran, Lee Sang Min, Lee Won Sik
Department of Laboratory Medicine, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
Paik Institute for Clinical Research, Inje University Busan Paik Hospital, Busan, Korea.
Blood Res. 2024 Dec 18;59(1):41. doi: 10.1007/s44313-024-00044-4.
The fifth World Health Organization (WHO) classification (2022 WHO) and International Consensus Classification (ICC) of myeloid neoplasms have recently been published. In this study, patients were reclassified according to the revised classification and their prognoses were analyzed to confirm the clinical utility of the new classifications.
We included 101 adult patients, 77 with acute myeloid leukemia (AML) and 24 with myelodysplastic neoplasms (MDS), who underwent bone marrow aspiration and next-generation sequencing (NGS) between August 2019 and July 2023. We reclassified the patients according to the revised criteria, examined the differences, and analyzed the prognosis using survival analysis.
According to the 2022 WHO and ICC, 23 (29.9%) patients and 32 (41.6%) patients were reclassified into different groups, respectively, due to the addition of myelodysplasia-related (MR) gene mutations to the diagnostic criteria or the addition of new entities associated with TP53 mutations. The median overall survival (OS) of patients with AML and MR gene mutations was shorter than that of patients in other AML groups; however, the difference was not significant. Patients with AML and TP53 mutation had a significantly shorter OS than the other AML group (p = 0.0014, median OS 2.3 vs 10.3 months). They also had significantly shorter OS than the AML and MR mutation group (p = 0.002, median OS 2.3 vs 9.6 months).
The revised classifications allow for a more detailed categorization based on genetic abnormalities, which may be helpful in predicting prognosis. AML with TP53 mutations is a new ICC category that has shown a high prognostic significance in a small number of cases.
世界卫生组织(WHO)第五版分类(2022年WHO分类)和国际共识分类(ICC)的髓系肿瘤分类最近已发布。在本研究中,根据修订后的分类对患者进行重新分类,并分析其预后,以确认新分类的临床实用性。
我们纳入了101例成年患者,其中77例为急性髓系白血病(AML),24例为骨髓增生异常肿瘤(MDS),这些患者在2019年8月至2023年7月期间接受了骨髓穿刺和下一代测序(NGS)。我们根据修订后的标准对患者进行重新分类,检查差异,并使用生存分析来分析预后。
根据2022年WHO分类和ICC,分别有23例(29.9%)患者和32例(41.6%)患者因诊断标准中增加了与骨髓增生异常相关(MR)基因突变或增加了与TP53突变相关的新实体而被重新分类到不同组。AML伴MR基因突变患者的中位总生存期(OS)短于其他AML组患者;然而,差异不显著。AML伴TP53突变患者的OS明显短于其他AML组(p = 0.0014,中位OS 2.3个月对10.3个月)。他们的OS也明显短于AML伴MR突变组(p = 0.002,中位OS 2.3个月对9.6个月)。
修订后的分类允许基于基因异常进行更详细的分类,这可能有助于预测预后。伴有TP53突变的AML是一个新的ICC类别,在少数病例中显示出较高的预后意义。