Back to Search Start Over

Aberrant Phenotypes in Acute Myeloid Leukemia and Its Relationship with Prognosis and Survival: A Systematic Review and Meta-Analysis.

Authors :
Pinheiro LHS
Trindade LD
Costa FO
Silva NL
Sandes AF
Nunes MAP
Correa CB
Almeida CAC
da Cruz GS
de Lyra Junior DP
Schimieguel DM
Source :
International journal of hematology-oncology and stem cell research [Int J Hematol Oncol Stem Cell Res] 2020 Oct 01; Vol. 14 (4), pp. 274-288.
Publication Year :
2020

Abstract

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, CD90 <superscript>low</superscript> , CD123 <superscript>high</superscript> , CD117 <superscript>high</superscript> , and three others were associated with good prognosis: CD19, CD98 <superscript>high</superscript> and CD117 <superscript>+</superscript> /CD15 <superscript>+</superscript> . 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.<br /> (Copyright © 2020 Tehran University of Medical Sciences.)

Details

Language :
English
ISSN :
2008-3009
Volume :
14
Issue :
4
Database :
MEDLINE
Journal :
International journal of hematology-oncology and stem cell research
Publication Type :
Academic Journal
Accession number :
33603989
Full Text :
https://doi.org/10.18502/ijhoscr.v14i4.4484