Evidence map›Paper›PMID 38978137›Full record

ArticleBMC research notes2024

Cytotoxic T-lymphocyte-associated 4 protein expression is associated with a high international prognostic score in advanced-stage classical Hodgkin lymphoma.

Flora Dameria Pangaribuan, Maria Francisca Ham, Mutiah Mutmainnah, Agnes Stephanie Harahap

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Article in BMC research notes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

2 citing papers in PubMed.

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4 · The record

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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

4 authors.

Flora Dameria PangaribuanAnatomical Pathology Department, Persahabatan Hospital, Jakarta, 13230, Indonesia.
Maria Francisca HamAnatomical Pathology Department, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo National Central General Hospital, Jakarta, 10430, Indonesia.
Mutiah MutmainnahFaculty of Medicine, Universitas Muhammadiyah Palembang, Palembang, 30263, Indonesia.
Agnes Stephanie HarahapAnatomical Pathology Department, Faculty of Medicine Universitas Indonesia, Dr. Cipto Mangunkusumo National Central General Hospital, Jakarta, 10430, Indonesia. agnes.stephanie01@ui.ac.id.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTwenty percent of all classical Hodgkin lymphoma (CHL) cases relapse and recur, especially in advanced stages with a high International Prognostic Score (IPS). Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) is a regulatory molecule that can inhibit the immune response and is related to tumor aggressiveness. This study aimed to determine the relationship between CTLA-4 expression in advanced-stage CHL and IPS, identifying it as a potential therapy target.

resultsIn advanced-stage CHL, the group with a high IPS exhibited significantly higher mean CTLA-4 expression compared to the group with a low IPS (p = 0.003).The group with Hb level < 10.5 g/dl, leukocyte count > 15,000/µL, lymphocyte count < 8%, albumin level < 4 g/dl, and stage 4 exhibited higher CTLA-4 expression than the other group, although only leukocyte count and stage showed statistical significance (p = 0.004 and p = 0.020). Mean CTLA-4 expression was 239.84 ± 76.36 for nodular sclerosis, 293.95 ± 147.94 for mixed cellularity, 271.4 ± 23.56 for lymphocyte depleted, and 225.2 for lymphocyte-rich subtypes. The results suggest that CTLA-4 expression is associated with adverse prognostic factors in the IPS for advanced-stage CHL, supporting the notion that immune checkpoints play a role in cancer progression.

Indexed as

CTLA-4 AntigenHodgkin DiseaseAdolescentAdultAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedNeoplasm StagingPrognosisYoung AdultBiomarkers, TumorCTLA-4 AntigenCTLA4 protein, humanAdvanced-stageCytotoxic T-lymphocyte-associated protein 4Hodgkin lymphomaInternational prognostic score

Identifiers

PMID38978137
PMCPMC11232165

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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.