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首页> 外文期刊>International journal of hematology-oncology and stem cell research. >Aberrant Phenotypes in Acute Myeloid Leukemia and Its Relationship with Prognosis and Survival: A Systematic Review and Meta-Analysis
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Aberrant Phenotypes in Acute Myeloid Leukemia and Its Relationship with Prognosis and Survival: A Systematic Review and Meta-Analysis

机译:急性髓性白血病的异常表型及其与预后和生存的关系:系统评价和荟萃分析

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Background: The aim of this review was to evaluate the influence of aberrant phenotypes in prognosis and survival in acute myeloid leukemia (AML) patients by multiparametric flow cytometry.Materials and Methods: Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, a review of PubMed, Scopus, Science Direct and Web of Science was carried out through 1998 to 2016, conducted by two reviewers independently, evaluating titles, abstracts and full-texts of the selected studies.Results: Ten studies were included on this review, in which the aberrant phenotype expression of 17 markers were detected in AML patients. From these, 11 aberrant phenotypes were associated with prognosis, which eight had shown negative impact on prognosis: CD7, CD56, CD15, CD2, CD3, CD90low, CD123high, CD117high, and three others were associated with good prognosis: CD19, CD98high and CD117+/CD15+. Meta-analysis showed that aberrant expression of CD56 as a poor prognostic marker with unfavorable outcomes is implicated in decreased overall survival in AML patients in 28 months (95% CI: 0.62 to 0.92).Conclusion: This was observed when there was association between CD56 expression and other prognostic factors, influencing on patients’ management care and treatment.
机译:背景:本综述的目的是评估异常表型对急性髓性白血病(AML)患者的预后和存活的影响。材料和方法:按照系统评价和荟萃分析的首选报告项目之后(Prisma )指导方针,通过1998年至2016年进行了一篇关于PubMed,Scopus,科学直接和科学网络的审查,由两位审稿人独立进行,评估所选研究的标题,摘要和全文。结果:包括十项研究该评价,其中在AML患者中检测到17个标记的异常表型表达。从这些中,11种异常表型与预后有关,八个表现出对预后的负面影响:CD7,CD56,CD15,CD2,CD3,CD90LOW,CD123,CD117High和其他三种与良好预后相关:CD19,CD98High和CD117 + / cd15 +。荟萃分析表明,CD56的异常表达作为具有不利结果的差的预后标志物涉及28个月内的AML患者的整体存活率下降(95%CI:0.62至0.92)。结论:当CD56之间存在关联时观察到这一点表达和其他预后因素,影响患者管理护理和治疗。

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