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EVI1 基因表达对急性髓系白血病患者预后意义的荟萃分析。

Prognostic significance of the EVI1 gene expression in patients with acute myeloid leukemia: a meta-analysis.

机构信息

Department of Hematology, West China Hospital, Sichuan University, No.37 GuoXue Xiang, Chengdu, 610041, Sichuan Province, China.

出版信息

Ann Hematol. 2019 Nov;98(11):2485-2496. doi: 10.1007/s00277-019-03774-z. Epub 2019 Sep 3.

Abstract

Ecotropic virus integration site-1 (EVI1) is frequently expressed in patients with acute myeloid leukemia (AML). Many studies have reported the potential poor prognostic impact of EVI1 higher expression (EVI1) in the AML patients; however, the conclusions previously reported have not been fully assessed and are still controversial. Therefore, we performed a meta-analysis to evaluate the prognostic significance of EVI1 in patients with AML. The primary endpoint was overall survival (OS), and the event-free survival (EFS) was selected as the secondary endpoint. We extracted the hazard ratio (HR) and their 95% confidence interval (CI) for the OS and EFS from the multivariate COX proportional hazard models. A total of 4767 AML patients from 11 studies up to 23 February 2019 were subjected to our meta-analysis. Pooled HRs suggested that EVI1 had an adverse impact on OS (HR = 1.52, 95%CI 1.24-1.86) and EFS (HR = 1.41, 95%CI 1.14-1.74) in AML patients. EVI1 was also associated with a shorter OS (HR = 1.73, 95%CI 1.43-2.11) and EFS (HR = 1.17, 95%CI 1.05-1.31) in AML patients with the intermediate cytogenetic risk (ICR) according to the National Comprehensive Cancer Network (NCCN), European leukemia network (ELN), or International System for Human Cytogenetic Nomenclature (ISCN). Furthermore, EVI1 appeared to be a poor prognosis indicator in patients with normal cytogenetics (NC) (HR for OS:2.01, 95%CI 1.32-3.05; HR for EFS 1.54, 95%CI 1.09-2.17) and young patients (HR for OS 1.30, 95%CI 1.09-1.55), respectively. This meta-analysis indicates EVI1 has an independent and significantly adverse prognostic impact on AML patients in the entire population, and this conclusion same applies to some subgroups like AML patients with ICR, NC, and young AML patients.

摘要

嗜同性病毒整合位点 1(EVI1)在急性髓细胞白血病(AML)患者中经常表达。许多研究报告了 EVI1 高表达(EVI1)在 AML 患者中潜在的不良预后影响;然而,以前报告的结论尚未得到充分评估,仍然存在争议。因此,我们进行了一项荟萃分析,以评估 EVI1 在 AML 患者中的预后意义。主要终点是总生存期(OS),无事件生存期(EFS)被选为次要终点。我们从多变量 COX 比例风险模型中提取 OS 和 EFS 的风险比(HR)及其 95%置信区间(CI)。截至 2019 年 2 月 23 日,共有来自 11 项研究的 4767 名 AML 患者纳入我们的荟萃分析。汇总 HR 表明,EVI1 对 AML 患者的 OS(HR=1.52,95%CI 1.24-1.86)和 EFS(HR=1.41,95%CI 1.14-1.74)有不良影响。EVI1 还与中间细胞遗传学风险(ICR)根据国家综合癌症网络(NCCN)、欧洲白血病网络(ELN)或国际人类细胞遗传学命名系统(ISCN)的 AML 患者的更短 OS(HR=1.73,95%CI 1.43-2.11)和 EFS(HR=1.17,95%CI 1.05-1.31)相关。此外,EVI1 似乎是正常核型(NC)(OS 的 HR:2.01,95%CI 1.32-3.05;EFS 的 HR:1.54,95%CI 1.09-2.17)和年轻患者(OS 的 HR:1.30,95%CI 1.09-1.55)预后不良的指标。这项荟萃分析表明,EVI1 对整个人群中的 AML 患者具有独立且显著的不良预后影响,这一结论同样适用于某些亚组,如 ICR、NC 和年轻 AML 患者。

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