急性髓性白血病和骨髓增生异常肿瘤:骨髓增生异常相关基因突变和TP53异常的临床意义。

IF 2.3 Q2 HEMATOLOGY
Hyunwoo Kim, Ja Young Lee, Shinae Yu, Eunkyoung Yoo, Hye Ran Kim, Sang Min Lee, Won Sik Lee
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引用次数: 0

摘要

目的:最近公布了世界卫生组织(WHO)第五次髓系肿瘤分类(2022 WHO)和国际共识分类(ICC)。在本研究中,根据修订后的分类对患者进行重新分类,并对其预后进行分析,以证实新分类的临床应用。方法:我们纳入了101例成人患者,其中77例患有急性髓性白血病(AML), 24例患有骨髓增生异常肿瘤(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,并使用生存分析分析预后。结果:根据2022年WHO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为不同的组。AML合并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,差异并不显著。AML和TP53突变患者的OS明显短于其他AML组(p = 0.0014,中位OS 2.3 vs 10.3个月)。他们的生存期也明显短于AML和MR突变组(p = 0.002,中位生存期2.3个月vs 9.6个月)。结论:修订后的分类允许基于遗传异常更详细的分类,这可能有助于预测预后。AML伴TP53突变是一种新的ICC类型,在少数病例中显示出很高的预后意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute myeloid leukemia and myelodysplastic neoplasms: clinical implications of myelodysplasia-related genes mutations and TP53 aberrations.

Purpose: 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.

Methods: 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.

Results: 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).

Conclusion: 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.

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来源期刊
Blood Research
Blood Research HEMATOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
64
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