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核心结合因子-急性髓系白血病(CBF-AML)中的继发性突变和细胞遗传学改变:一项系统评价和荟萃分析

Secondary mutational and cytogenetic alterations in core binding factor - Acute myeloid leukemia (CBF-AML): A systematic review and meta-analysis.

作者信息

Javidan Amin, Azarboo Alireza, Jalali Sayeh, Fallahtafti Parisa, Azimi Shahrabi Yeganeh, Yaghmaie Marjan, Fathi Amir T

机构信息

School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Crit Rev Oncol Hematol. 2025 Aug;212:104770. doi: 10.1016/j.critrevonc.2025.104770. Epub 2025 May 22.

Abstract

BACKGROUND

Acute myeloid leukemia (AML) with core-binding factor alterations (CBF-AML) is a notable subtype characterized by specific genetic alterations and a relatively favorable prognosis. Despite this, a significant proportion of CBF-AML patients experience relapse, indicating the potential prognostic role of other co-present cytogenetic abnormalities and gene mutations.

METHODS

A comprehensive search of PubMed, Embase, Web of Science, and Scopus was conducted until April 2024. Studies evaluating the prognostic impact of secondary cytogenetic abnormalities and gene mutations in CBF-AML were included. Data extraction and quality assessment were independently performed by two reviewers. Statistical analysis was conducted using the "meta" package in R.

RESULTS

59 studies met the inclusion criteria. Mutations in the c-kit gene were significantly associated with decreased overall survival (OS) and disease-free survival (DFS) at 1, 5, and 10-year intervals. Patients with high c-kit expression also showed poorer survival outcomes. The presence of FLT3-ITD mutations was also correlated with lower survival rates. N-RAS mutations were found to have a variable impact on prognosis, with some studies indicating a negative effect on OS and DFS, while others showed no significant impact. Certain secondary cytogenetic abnormalities, such as loss of sex chromosomes and trisomy 8, were found to negatively affect prognosis, while trisomy 22 was found to increase 5-year RFS.

CONCLUSION

Secondary cytogenetic abnormalities and mutations, notably c-KIT and FLT3-ITD, were linked to poorer survival in CBF-AML. Trisomy 8 also worsened prognosis, while N-RAS mutations showed minimal impact. These findings highlight the value of genetic profiling for risk stratification and personalized therapy. Future research should explore targeted treatments for high-risk subgroups to improve outcomes and reduce relapse rates.

摘要

背景

伴有核心结合因子改变的急性髓系白血病(CBF-AML)是一种显著的亚型,其特征为特定的基因改变和相对良好的预后。尽管如此,相当一部分CBF-AML患者会复发,这表明其他同时存在的细胞遗传学异常和基因突变可能具有预后作用。

方法

截至2024年4月,对PubMed、Embase、Web of Science和Scopus进行了全面检索。纳入评估CBF-AML中继发性细胞遗传学异常和基因突变的预后影响的研究。由两名审阅者独立进行数据提取和质量评估。使用R语言中的“meta”包进行统计分析。

结果

59项研究符合纳入标准。c-kit基因的突变与1年、5年和10年的总生存期(OS)和无病生存期(DFS)降低显著相关。c-kit高表达的患者也显示出较差的生存结果。FLT3-ITD突变的存在也与较低的生存率相关。发现N-RAS突变对预后有不同影响,一些研究表明对OS和DFS有负面影响,而另一些研究则显示无显著影响。某些继发性细胞遗传学异常,如性染色体缺失和8号染色体三体,被发现对预后有负面影响,而22号染色体三体被发现可提高5年无复发生存率(RFS)。

结论

继发性细胞遗传学异常和突变,尤其是c-KIT和FLT3-ITD,与CBF-AML患者较差的生存相关。8号染色体三体也使预后恶化,而N-RAS突变影响最小。这些发现凸显了基因谱分析在风险分层和个性化治疗中的价值。未来的研究应探索针对高危亚组的靶向治疗,以改善预后并降低复发率。

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