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Mol Cytogenet. 2022 Oct 5;15(1):43. doi: 10.1186/s13039-022-00621-1.
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Secondary cytogenetic abnormalities in core-binding factor AML harboring inv(16) vs t(8;21).伴有inv(16)与t(8;21)的核心结合因子急性髓系白血病中的继发性细胞遗传学异常
Blood Adv. 2021 May 25;5(10):2481-2489. doi: 10.1182/bloodadvances.2020003605.
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Clinical profile, cytogenetics and treatment outcomes of adult acute myeloid leukemia.成人急性髓系白血病的临床特征、细胞遗传学及治疗结果
J Cancer Res Ther. 2020 Jan-Mar;16(1):18-22. doi: 10.4103/jcrt.JCRT_1162_16.
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Cytogenetic profile of a representative cohort of young adults with de novo acute myéloblastic leukaemia in Morocco.摩洛哥年轻成人初发急性髓系白血病代表性队列的细胞遗传学特征
Cancer Genet. 2019 Oct;238:1-9. doi: 10.1016/j.cancergen.2019.06.010. Epub 2019 Jun 15.
5
Characteristics of De Novo Acute Myeloid Leukemia Patients in Palestine: Experience of An-Najah National University Hospital.巴勒斯坦初发急性髓系白血病患者的特征:纳贾赫国立大学医院的经验
Asian Pac J Cancer Prev. 2017 Sep 27;18(9):2459-2464. doi: 10.22034/APJCP.2017.18.9.2459.
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Sex chromosome changes in leukemia: cytogenetics and molecular aspects.白血病中的性染色体改变:细胞遗传学与分子层面
Hematology. 2018 Apr;23(3):139-147. doi: 10.1080/10245332.2017.1375063. Epub 2017 Sep 10.
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Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel.成人急性髓系白血病的诊断与管理:2017年国际专家小组的欧洲白血病网络(ELN)建议
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越南南部初发急性髓系白血病的细胞遗传学特征。

Cytogenetic Characteristics of de novo Acute Myeloid Leukemia in Southern Vietnam.

机构信息

Department of Hematology, Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.

Department of Hematology, Cho Ray Hospital, Ho Chi Minh City, Vietnam.

出版信息

Asian Pac J Cancer Prev. 2023 May 1;24(5):1789-1795. doi: 10.31557/APJCP.2023.24.5.1789.

DOI:10.31557/APJCP.2023.24.5.1789
PMID:37247302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10495905/
Abstract

BACKGROUND

The cytogenetic characteristics are important factors for risk stratification at diagnosis of acute myeloid leukemia (AML); however, cytogenetic profile of Vietnamese patients with AML remains undetermined. In this study, we present the chromosomal data of de novo AML patients in Southern Vietnam.

METHODS

We performed cytogenetic testing for 336 AML patients using G banding. If the patients had suspected abnormalities, fluorescence in situ hybridization with probes of inv(3)(q21q26)/t(3;3)(q21;q26), 5q31, 7q31, t(8;21)(q21.3;q22), 11q23, t(15;17)(q24;q21), inv(16)(p13q22)/t(16;16)(p13;q22)were analyzed. Patients without above aberrations or with normal karyotype were tested by fluorescence in situ hybridization using probe 11q23.

RESULTS

We found that the median age was 39 years. According to French - American - British classification, AML-M2 is the most frequent type with 35.1%. Chromosomal abnormalities were detected in 208 cases, accounting for 61.9%. Among structural abnormalities, t(15;17) was the most common (19.6%), followed by t(8;21) and inv (16)/t(16;16) in 10.1% and 6.2%, respectively. In perspective of chromosomal numerical abnornmalities, loss of sex chromosomes are the most common (7.7%), followed by +8 in 6.8%, -7/del(7q) in 4.4%, +21 in 3.9% and -5/del (5q) in 2.1%. The prevalence of addditional cytogenetic aberrations accompanying with t(8;21) and inv(16)/t(16;16) were 82.4% and 52.4%, repectively. None of +8 cases was associated with t(8;21). Regarding cytogenetic risk assessment according to European Leukemia Net 2017, there were 121 (36%) patients in favorable-risk, 180 (53.6%) in intermediate-risk and 35 (10.4%) in adverse-risk group.

CONCLUSION

In conclusion, this is the first comprehensive cytogenetic profile of Vietnamese patients diagnosed with de novo AML, which helps clinical doctors in prognostic classification for AML patients in Southern Vietnam.

摘要

背景

细胞遗传学特征是急性髓细胞白血病(AML)诊断时进行风险分层的重要因素;然而,越南 AML 患者的细胞遗传学特征仍未确定。本研究介绍了越南南部初诊 AML 患者的染色体数据。

方法

我们对 336 例 AML 患者进行了 G 显带染色体核型分析。如果患者有可疑异常,我们会用探针 inv(3)(q21q26)/t(3;3)(q21;q26)、5q31、7q31、t(8;21)(q21.3;q22)、11q23、t(15;17)(q24;q21)、inv(16)(p13q22)/t(16;16)(p13;q22)进行荧光原位杂交(FISH)检测。无上述异常或核型正常的患者用探针 11q23 进行 FISH 检测。

结果

我们发现中位年龄为 39 岁。根据法美英分类,AML-M2 是最常见的类型,占 35.1%。208 例患者发现染色体异常,占 61.9%。在结构异常中,t(15;17)最为常见(19.6%),其次是 t(8;21)和 inv(16)/t(16;16),分别占 10.1%和 6.2%。在染色体数目异常方面,性染色体丢失最为常见(7.7%),其次是+8(6.8%)、-7/del(7q)(4.4%)、+21(3.9%)和-5/del(5q)(2.1%)。t(8;21)和 inv(16)/t(16;16) 患者的附加细胞遗传学异常发生率分别为 82.4%和 52.4%。没有+8 病例与 t(8;21)相关。根据 2017 年欧洲白血病网络(European Leukemia Net)的标准,121 例(36%)患者为低危、180 例(53.6%)为中危、35 例(10.4%)为高危。

结论

总之,这是越南初诊 AML 患者的首个全面细胞遗传学特征,有助于越南南部 AML 患者的临床医生进行预后分类。