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土耳其成人 AML 患者的细胞遗传学特征:与文献全面比较的单中心研究。

Cytogenetic profile of adult AML patients in Turkey: a single center study with comprehensive comparison with literature.

机构信息

Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Medical Biology.

Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Internal Medicine, Division of Hematology.

出版信息

Afr Health Sci. 2022 Sep;22(3):183-191. doi: 10.4314/ahs.v22i3.21.

Abstract

BACKGROUND

Cytogenetic findings are important prognostic factors in acute myeloid leukemia. Large systematic data about chromosomal characteristics of Turkish AML patients have not been reported to date.

OBJECTIVES

The karyotypic profiles of 157 adult AML patients were evaluated retrospectively and compared with other reports from different populations.

METHODS

Cytogenetics analyses were performed on bone marrow samples using G-banding. Patients were categorized according to their cytogenetic results into four groups with the addition of a normal karyotyped group to the favorable, intermediate and adverse groups of European Leukemia Network.

RESULTS

Cytogenetic analyses were carried out successfully in 138 patients (88%). Abnormal karyotypes were found in 79 (57.2%) patients of which 13 (9.4%) were in favorable, 37 (26.8%) in intermediate and 29 (21%) in adverse groups. t(8;21) (5%) was the most common favorable abnormality while monosomal karyotypes (15.9%) in adverse group.

CONCLUSION

This single center study is the most comprehensive study about the cytogenetic profile of acute myeloid leukemia in Turkey with comparison of other population-based studies. While there were similarities and differences with different publications, our results did not show a marked tendency to the findings of any specific geographic region.

摘要

背景

细胞遗传学发现是急性髓细胞白血病的重要预后因素。目前尚未报道关于土耳其 AML 患者染色体特征的大型系统数据。

目的

回顾性评估了 157 例成年 AML 患者的核型谱,并与来自不同人群的其他报告进行了比较。

方法

使用 G 带对骨髓样本进行细胞遗传学分析。根据细胞遗传学结果将患者分为四组,并在欧洲白血病网络的有利、中间和不良组中加入正常核型组。

结果

成功进行了 138 例(88%)患者的细胞遗传学分析。在 79 例(57.2%)异常核型患者中,有 13 例(9.4%)为有利组,37 例(26.8%)为中间组,29 例(21%)为不良组。t(8;21)(5%)是最常见的有利异常,而不良组的单体核型(15.9%)。

结论

这是土耳其关于急性髓细胞白血病细胞遗传学特征的最全面的单中心研究,并与其他基于人群的研究进行了比较。虽然与不同出版物存在相似和差异,但我们的结果并未显示出任何特定地理区域发现的明显倾向。

相似文献

本文引用的文献

1
Why classical cytogenetics still matters in acute myeloid leukemia.为何经典细胞遗传学在急性髓系白血病中仍至关重要。
Expert Rev Hematol. 2020 Feb;13(2):95-97. doi: 10.1080/17474086.2020.1711733. Epub 2020 Jan 14.
2
Acute myeloid leukaemia.急性髓系白血病。
Lancet. 2018 Aug 18;392(10147):593-606. doi: 10.1016/S0140-6736(18)31041-9. Epub 2018 Aug 2.

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