Evidence map›Paper›PMID 28646224›Full record

SynthesisScientific reports2017

Role of new Immunophenotypic Markers on Prognostic and Overall Survival of Acute Myeloid Leukemia: a Systematic Review and Meta-Analysis.

A F O Costa, D L Menezes, L H S Pinheiro, A F Sandes, M A P Nunes, D P Lyra Junior, D M Schimieguel

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

A F O CostaDepartment of Pharmacy, Laboratory of Hematology, Federal University of Sergipe, Aracaju, Sergipe, Brazil. amandafernandes@hotmail.com.ORCID 0000-0002-1898-2896
D L MenezesDepartment of Pharmacy, Laboratory of Hematology, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
L H S PinheiroDepartment of Pharmacy, Laboratory of Hematology, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
A F SandesFleury Group, Hematology Division, São Paulo, São Paulo, Brazil.
M A P NunesDepartment of Medicine, Federal University of Sergipe, Aracaju, Sergipe, Brazil.ORCID 0000-0001-5244-5843
D P Lyra JuniorDepartment of Pharmacy, Laboratory of Hematology, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
D M SchimieguelDepartment of Pharmacy, Laboratory of Hematology, Federal University of Sergipe, Aracaju, Sergipe, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite technological advances, the prognosis and survival of acute myeloid leukemia (AML) adult patients remain low, compared with other hematologic malignancies. Some antigens detected by immunophenotyping may soon play a significant role in the pathophysiologic, prognostic, and overall survival (OS) rate of AML patients. Therefore, we conducted a systematic review and meta-analysis of PubMed, Scopus, Science Direct, Web of Science, and the Cochrane Library (using PRISMA guidelines). We analyzed 11 studies and 13 antigens, detected through the immunophenotyping of 639 patients. From them, twelve exhibited a negative impact with AML prognosis. The meta-analysis demonstrated a high expression of AML markers, which have been associated with a decrease in survival over 10 months (RR 2.55; IC 95%; 1.49-4.37) and over 20 months (RR 2.46; IC 95%; 1.75-3.45). Knowing that the expression of immunophenotypic markers, which are not used on a routine basis, might be able to influence disease behavior, looks promising. However, they have been associated with a poor prognosis as well as a decrease in survival. This may allow for different chemotherapeutical protocols, including future studies for new therapeutic targets.

Indexed as

BiomarkersFemaleHumansImmunophenotypingLeukemia, Myeloid, AcuteMalePrognosisPublication BiasBiomarkers

Identifiers

PMID28646224
PMCPMC5482890

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.