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- 突变型急性髓系白血病中的细胞遗传学异常。

Cytogenetic abnormalities in -mutated acute myeloid leukemia.

机构信息

Department of Hematology, Institute of Hematology, Changhai Hospital 200433, Shanghai, China.

出版信息

Leuk Lymphoma. 2022 Aug;63(8):1956-1963. doi: 10.1080/10428194.2022.2045600. Epub 2022 Feb 28.

Abstract

acute myeloid leukemia (AML) has been identified as a distinct entity of myeloid neoplasms according to the 2017 European LeukemiaNet (ELN) guidelines. It confers a favorable prognosis regardless of cytogenetic abnormalities. We evaluated 418 newly diagnosed AML patients to test the validity of this hypothesis. Seventy-four patients with AML showed a good response to induction and a relatively favorable prognosis. Abnormal karyotypes were observed in 15 patients. Chromosomal abnormalities were significantly associated with a worse prognosis in AML patients (5-year overall survival (OS): 38.9 ± 12.9%,  .037; event-free survival (EFS): 33.3 ± 12.2%,  .043, respectively). Four patients with abnormal karyotypes who underwent allogeneic hematopoietic stem cell transplantation (alloHSCT) during CR1 had longer survival than those who received chemotherapy only. Multivariable analysis revealed abnormal karyotypes independently predicted OS and EFS among AML patients. In summary, cytogenetic abnormalities are strong prognostic indicators in AML. Therefore, they should be classified accordingly, and alloHSCT should be performed on selected patients during CR1.

摘要

根据 2017 年欧洲白血病网络(ELN)指南,急性髓系白血病(AML)已被确定为髓系肿瘤的一个独特实体。它具有良好的预后,无论细胞遗传学异常如何。我们评估了 418 例新诊断的 AML 患者,以检验这一假设的有效性。74 例 AML 患者对诱导治疗反应良好,预后相对较好。15 例患者存在异常核型。染色体异常与 AML 患者预后较差显著相关(5 年总生存率(OS):38.9±12.9%,.037;无事件生存率(EFS):33.3±12.2%,.043)。4 例在 CR1 期间接受异基因造血干细胞移植(alloHSCT)的核型异常患者的生存时间长于仅接受化疗的患者。多变量分析显示,核型异常独立预测 AML 患者的 OS 和 EFS。总之,细胞遗传学异常是 AML 的强烈预后指标。因此,应根据这些异常进行分类,并在 CR1 期间为选定的患者进行 alloHSCT。

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