Evidence map›Paper›PMID 38809650›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

Prognostic effect of CTLA4/LAG3 Expression by T-Cells Subsets on Acute Myeloid Leukemia Patients.

Wesam El Dosoky, Salah Aref, Nadia El Menshawy, Ahmed Ramez, Tarek Abou Zaid, Mohamed Aref, Doaa Atia

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
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  8. Bone marrow immune cells and drug resistance in acute myeloid leukemia.Experimental biology and medicine (Maywood, N.J.) · 2025
    Review
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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.

Wesam El DosokyHematology Unit, Mansoura University Oncology Center, Mansoura University, Egypt.
Salah ArefHematology Unit, Mansoura University Oncology Center, Mansoura University, Egypt.ORCID 0000-0002-4822-5204
Nadia El MenshawyHematology Unit, Mansoura University Oncology Center, Mansoura University, Egypt.
Ahmed RamezMansoura University Oncology Center, Mansoura University, Egypt.
Tarek Abou ZaidMansoura University Oncology Center, Mansoura Faculty of Medicine, Mansoura University, Egypt.
Mohamed ArefMansoura University Oncology Center, Mansoura Faculty of Medicine, Mansoura University, Egypt.
Doaa AtiaMansoura University Oncology Center, Mansoura Faculty of Medicine, Mansoura University, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDeregulation of immune checkpoint is an important point in cancer evolution as well as patients outcome. T-cells is an important arm in immunity against cancer. This study aimed to assess CTLA4/LAG3 expression on different T-cell subsets and its effect on disease outcome.

methodsThis study included 81 newly diagnosed Egyptian adult AML patients. For each one of the patients CTLA4/ LAG3 expression on T-cell subsets was identified by flowcytometry before start of induction chemotherapy.

resultsTotal CD3 count in AML patients was lower than control. LAG3 expression were significantly higher in total CD3, T-cell subsets (CD4, CD8) as compared to healthy control. Moreover, co-expression of LAG3/CTLA4 on T-cell subsets were significantly higher in AML as compared to healthy control . NPM-/ FLT3+ was significantly associated with high LAG3 expression in T-cells subsets as compared to other molecular subtypes. Shorter OS, DFS were significantly associated with higher expression of LAG3 on T-cells subsets as compared to patients harbor low expression. COX regression analysis revealed that high expression of CD3/LAG3, CD4/LAG3, CD8/LAG4, CD3/CTLA4/LAG3 were considered a poor prognostic risk factor.

conclusionHigh LAG3/CTLA4 expression could predict AML Patients' outcome Conclusion: Our findings indicated that high expression of LAG3/CTL4 on T cells subsets identify a subgroup of AML patients with poor prognosis.

Indexed as

Antigens, CDBiomarkers, TumorCTLA-4 AntigenLeukemia, Myeloid, AcuteLymphocyte Activation Gene 3 ProteinT-Lymphocyte SubsetsAdolescentAdultCase-Control StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisSurvival RateAntigens, CDBiomarkers, TumorCTLA-4 AntigenCTLA4 protein, humanLag3 protein, humanLymphocyte Activation Gene 3 ProteinAMLCTLA4LAG3T cell :

Identifiers

PMID38809650
PMCPMC11318815

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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.