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根据 2016 年 WHO 分类对急性髓系白血病进行重新分类。

Reclassification of Acute Myeloid Leukemia According to the 2016 WHO Classification.

机构信息

Department of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Department of Hematology, Seoul St. Mary's Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Ann Lab Med. 2019 May;39(3):311-316. doi: 10.3343/alm.2019.39.3.311.

DOI:10.3343/alm.2019.39.3.311
PMID:30623623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6340847/
Abstract

We reviewed our leukemia database to reclassify 610 patients previously diagnosed as having acute myeloid leukemia (AML) according to the updated 2016 WHO classification. Nine patients were categorized as having myelodysplastic syndrome and myeloid neoplasms with germline predisposition. AML with recurrent genetic abnormalities accounted for 57.4% (345/601) of the patients under the 2016 WHO classification. AML with mutated was the most common form (16.5%), with the majority associated with monocytic differentiation (63.6%). AML with double mutations accounted for 8.3% of these cases, and the majority were previously diagnosed as AML with/without maturation (78.0%). These newly classified mutations were mutually exclusive without overlapping with other forms of AML with recurrent genetic abnormalities. AML with mutated and AML with myelodysplasia-related changes comprised the oldest patients, whereas AML with included the youngest patients. The leukocyte count was highest in AML with mutated , and the percentage of peripheral blood blasts was the highest in AML with double mutations. Our results indicate that implementation of the 2016 WHO classification of AML would not pose major difficulties in clinical practice. Hematopathologists should review and prepare genetic tests for the new classification, according to their clinical laboratory conditions.

摘要

我们回顾了我们的白血病数据库,根据 2016 年 WHO 分类标准,重新分类了 610 例先前诊断为急性髓系白血病(AML)的患者。9 例患者被归类为骨髓增生异常综合征和具有种系易感性的髓系肿瘤。在 2016 年 WHO 分类标准下,具有复发性遗传异常的 AML 占 601 例患者的 57.4%(345/601)。突变的 AML 是最常见的形式(16.5%),大多数与单核细胞分化相关(63.6%)。AML 中存在双 突变占这些病例的 8.3%,且大多数以前被诊断为 AML 伴/不伴成熟(78.0%)。这些新分类的突变是相互排斥的,与其他形式的复发性遗传异常的 AML 没有重叠。突变的 AML 和伴骨髓增生异常相关改变的 AML 患者年龄最大,而 突变的 AML 患者年龄最小。突变的 AML 中的白细胞计数最高,双 突变的 AML 中的外周血原始细胞比例最高。我们的结果表明,在临床实践中实施 2016 年 WHO 分类标准 AML 不会带来重大困难。血液病理学家应根据其临床实验室条件,审查和准备新分类的基因检测。

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本文引用的文献

1
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia.2016 年版世界卫生组织髓系肿瘤和急性白血病分类。
Blood. 2016 May 19;127(20):2391-405. doi: 10.1182/blood-2016-03-643544. Epub 2016 Apr 11.
2
A clinical grade sequencing-based assay for CEBPA mutation testing: report of a large series of myeloid neoplasms.一种基于测序的临床级CEBPA突变检测分析方法:大量髓系肿瘤病例报告
J Mol Diagn. 2015 Jan;17(1):76-84. doi: 10.1016/j.jmoldx.2014.09.007. Epub 2014 Nov 6.
3
Favorable prognosis of biallelic CEBPA gene mutations in acute myeloid leukemia patients: a meta-analysis.
Real-World Treatment Patterns and Clinical Outcomes in Korean Patients With AML Ineligible for First-Line Intensive Chemotherapy: A Subanalysis of the CURRENT Study, a Non-Interventional, Retrospective Chart Review.
在不适合一线强化化疗的韩国 AML 患者中真实世界的治疗模式和临床结局:CURRENT 研究的一项亚分析,这是一项非干预性、回顾性图表审查。
J Korean Med Sci. 2023 Nov 13;38(44):e345. doi: 10.3346/jkms.2023.38.e345.
4
Identification of TLN1 as a prognostic biomarker to effect cell proliferation and differentiation in acute myeloid leukemia.鉴定 TLN1 作为急性髓系白血病中影响细胞增殖和分化的预后生物标志物。
BMC Cancer. 2022 Sep 29;22(1):1027. doi: 10.1186/s12885-022-10099-0.
5
Risk stratification by 30-day prognostic factors of clinical outcomes after granulocyte transfusion in acute myeloid leukemia: A single-center retrospective study.粒细胞输注后 30 天临床结局的预后因素风险分层:一项单中心回顾性研究。
PLoS One. 2022 Aug 30;17(8):e0273827. doi: 10.1371/journal.pone.0273827. eCollection 2022.
6
Genetic Characteristics According to Subgroup of Acute Myeloid Leukemia with Myelodysplasia-Related Changes.伴有骨髓发育异常相关改变的急性髓系白血病亚组的遗传特征
J Clin Med. 2022 Apr 23;11(9):2378. doi: 10.3390/jcm11092378.
7
Kinesin family member 2A acts as a potential prognostic marker and treatment target via interaction with PI3K/AKT and RhoA/ROCK pathways in acute myeloid leukemia.驱动蛋白家族成员 2A 通过与 PI3K/AKT 和 RhoA/ROCK 通路相互作用,成为急性髓系白血病的潜在预后标志物和治疗靶点。
Oncol Rep. 2022 Jan;47(1). doi: 10.3892/or.2021.8229. Epub 2021 Nov 18.
8
Roles of Histone Deacetylases in Acute Myeloid Leukemia With Fusion Proteins.组蛋白去乙酰化酶在伴有融合蛋白的急性髓系白血病中的作用
Front Oncol. 2021 Sep 1;11:741746. doi: 10.3389/fonc.2021.741746. eCollection 2021.
9
Changing the frequency and spectra of chromosomal aberrations in Korean patients with acute leukemia in a tertiary care hospital.三级护理医院中韩国急性白血病患者染色体畸变频率和谱的变化
Blood Res. 2020 Dec 31;55(4):225-245. doi: 10.5045/br.2020.2020255.
10
Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review.两例罕见的伴有t(8;16)(p11.2;p13.3)和1q重复的急性髓系白血病:病例报告及文献复习
Mol Cytogenet. 2020 Aug 25;13:37. doi: 10.1186/s13039-020-00507-0. eCollection 2020.
急性髓系白血病患者双等位基因CEBPA基因突变的良好预后:一项荟萃分析。
Eur J Haematol. 2015 May;94(5):439-48. doi: 10.1111/ejh.12450. Epub 2015 Jan 22.
4
Detection of minimal residual disease in NPM1-mutated acute myeloid leukemia by next-generation sequencing.通过下一代测序检测NPM1突变型急性髓系白血病中的微小残留病
Mod Pathol. 2014 Nov;27(11):1438-46. doi: 10.1038/modpathol.2014.57. Epub 2014 Apr 18.
5
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis.CEBPA 双突变急性髓系白血病在伴有 TET2 和 GATA2 改变的病例中,有 76.8% 同时存在分子突变,这些突变影响预后。
Br J Haematol. 2013 Jun;161(5):649-658. doi: 10.1111/bjh.12297. Epub 2013 Mar 25.
6
Acute myeloid leukemia with biallelic CEBPA gene mutations and normal karyotype represents a distinct genetic entity associated with a favorable clinical outcome.伴有双等位基因 CEBPA 基因突变和正常核型的急性髓细胞白血病是一种独特的遗传实体,与良好的临床转归相关。
J Clin Oncol. 2010 Feb 1;28(4):570-7. doi: 10.1200/JCO.2008.21.6010. Epub 2009 Dec 28.
7
Acute myeloid leukemia with mutated NPM1: diagnosis, prognosis and therapeutic perspectives.伴 NPM1 基因突变的急性髓系白血病:诊断、预后和治疗前景。
Curr Opin Oncol. 2009 Nov;21(6):573-81. doi: 10.1097/CCO.0b013e3283313dfa.
8
AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features.伴有NPM1突变且核型正常或异常的急性髓系白血病具有重叠的生物学、病理学、免疫表型和预后特征。
Blood. 2009 Oct 1;114(14):3024-32. doi: 10.1182/blood-2009-01-197871. Epub 2009 May 8.
9
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes.世界卫生组织(WHO)髓系肿瘤和急性白血病分类的2008年修订版:基本原理及重要变化
Blood. 2009 Jul 30;114(5):937-51. doi: 10.1182/blood-2009-03-209262. Epub 2009 Apr 8.
10
Prevalence and prognostic implications of CEBPA mutations in pediatric acute myeloid leukemia (AML): a report from the Children's Oncology Group.儿童急性髓系白血病(AML)中CEBPA突变的患病率及其预后意义:来自儿童肿瘤协作组的报告
Blood. 2009 Jun 25;113(26):6558-66. doi: 10.1182/blood-2008-10-184747. Epub 2009 Mar 20.