Pinheiro Lucio Henrique Sousa, Trindade Louise Dantas, Costa Fernandes de Oliveira, Silva Nathanielly de Lima, Sandes Alex Freire, Nunes Marco Antônio Prado, Correa Cristiane Bani, Almeida Carlos Arthur Cardoso, da Cruz Geydson Silveira, de Lyra Junior Divaldo Pereira, Schimieguel Dulce Marta
Department of Pharmacy, Laboratory of Hematology, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil.
Department of Medicine, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Int J Hematol Oncol Stem Cell Res. 2020 Oct 1;14(4):274-288. doi: 10.18502/ijhoscr.v14i4.4484.
: 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. : 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. : 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, CD90, CD123, CD117, and three others were associated with good prognosis: CD19, CD98 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). This was observed when there was association between CD56 expression and other prognostic factors, influencing on patients' management care and treatment.
本综述的目的是通过多参数流式细胞术评估异常表型对急性髓系白血病(AML)患者预后和生存的影响。遵循系统评价和Meta分析的首选报告项目(PRISMA)指南,两位审稿人独立对1998年至2016年期间的PubMed、Scopus、Science Direct和科学网进行了检索,评估所选研究的标题、摘要和全文。本综述纳入了10项研究,其中在AML患者中检测到17种标志物的异常表型表达。其中,11种异常表型与预后相关,8种对预后有负面影响:CD7、CD56、CD15、CD2、CD3、CD90、CD123、CD117,另外3种与良好预后相关:CD19、CD98和CD117/CD15。Meta分析表明,CD56作为不良预后标志物的异常表达与不良结局相关,这与AML患者28个月时总生存期降低有关(95%CI:0.62至0.92)。当CD56表达与其他预后因素相关时观察到这一点,这会影响患者的管理护理和治疗。