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核心结合因子急性髓系白血病中C-KIT突变的预后重要性:一项系统综述

Prognostic Importance of C-KIT Mutations in Core Binding Factor Acute Myeloid Leukemia: A Systematic Review.

作者信息

Ayatollahi Hossein, Shajiei Arezoo, Sadeghian Mohammad Hadi, Sheikhi Maryam, Yazdandoust Ehsan, Ghazanfarpour Masumeh, Shams Seyyede Fatemeh, Shakeri Sepideh

机构信息

Cancer Molecular Pathology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Department of Hematology and Blood Bank, Cancer Molecular Pathology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Hematol Oncol Stem Cell Ther. 2017 Mar;10(1):1-7. doi: 10.1016/j.hemonc.2016.08.005. Epub 2016 Sep 3.

Abstract

OBJECTIVE/BACKGROUND: Acute myeloid leukemia (AML) is defined as leukemic blast reproduction in bone marrow. Chromosomal abnormalities form different subgroups with joint clinical specifications and results. t(8;21)(q22;q22) and inv(16)(p13;q22) form core binding factor-AML (CBF-AML). c-kit mutation activation occurs in 12.8-46.1% of adults with CBF leukemia. These mutations occur in 20-25% of t(8;21) and 30% of inv(16) cases.

METHODS

In this systematic review, we searched different databases, including PubMed, Scopus, and Embase. Selected articles were measured based on the inclusion criteria of this study and initially compared in terms of titles or abstracts. Finally, articles relevant to the subject of this review were retrieved in full text. Twenty-two articles matched the inclusion criteria and were selected for this review.

RESULTS

In this study, c-kit mutations were associated with poor prognosis in AML patients with t(8;21) and inv(16). In addition, these mutations had better prognostic effects on AML patients with inv(16) compared with those with t(8;21).

CONCLUSION

According to the results of this study, c-kit mutations have intense, harmful effects on the relapse and white blood cell increase in CBF-AML adults. However, these mutations have no significant prognostic effects on patients.

摘要

目的/背景:急性髓系白血病(AML)被定义为骨髓中白血病母细胞的增殖。染色体异常形成具有共同临床特征和结果的不同亚组。t(8;21)(q22;q22)和inv(16)(p13;q22)形成核心结合因子急性髓系白血病(CBF-AML)。c-kit突变激活在12.8%至46.1%的成年CBF白血病患者中发生。这些突变发生在20%至25%的t(8;21)病例和30%的inv(16)病例中。

方法

在这项系统评价中,我们检索了不同的数据库,包括PubMed、Scopus和Embase。根据本研究的纳入标准对所选文章进行评估,并首先根据标题或摘要进行比较。最后,全文检索与本综述主题相关的文章。22篇文章符合纳入标准并被选入本综述。

结果

在本研究中,c-kit突变与t(8;21)和inv(16)的AML患者预后不良相关。此外,与t(8;21)患者相比,这些突变对inv(16)的AML患者具有更好的预后影响。

结论

根据本研究结果,c-kit突变对成年CBF-AML患者的复发和白细胞增加有强烈的有害影响。然而,这些突变对患者没有显著的预后影响。

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