Evidence map›Paper›PMID 39122531›Full record

ArticleDermatology practical & conceptual2024

Relationship Between PD-L1, PD-1, CD8 and Clinicopathological Factors in Primary SCCs.

Preslav Vasilev, Savelina Popovska, Elitsa Petrova Kraevska, Martin Karamanliev, Dobromir Dimitrov, Ivelina Yordanova

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Article in Dermatology practical & conceptual, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Preslav VasilevDepartment of Dermatology, Venereology and Allergology, Faculty of Medicine, Medical University-Pleven, Bulgaria.
Savelina PopovskaDepartment of General and Clinical Pathology, Faculty of Medicine, Medical University-Pleven, Bulgaria.
Elitsa Petrova KraevskaDepartment of General and Clinical Pathology, Faculty of Medicine, Medical University-Pleven, Bulgaria.
Martin KaramanlievSurgical Oncology Department, University Hospital "Dr. Georgi Stranski", Faculty of Medicine, Medical University-Pleven, Bulgaria.
Dobromir DimitrovSurgical Oncology Department, University Hospital "Dr. Georgi Stranski", Faculty of Medicine, Medical University-Pleven, Bulgaria.
Ivelina YordanovaDepartment of Dermatology, Venereology and Allergology, Faculty of Medicine, Medical University-Pleven, Bulgaria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSquamous cell carcinoma of the skin (SCCs) is the second most common skin cancer, with continuously increasing incidence. Programmed cell death ligand 1 (PD-L1), programmed cell death 1 receptor (PD-1), and CD8 expression in primary SCCs have not been described in many studies.

objectiveWe investigated the association between PD-L1, PD-1, CD8, and clinicopathological prognostic factors for recurrence, metastasis, and mortality of SCCs. PATIENTS AND

methodsImmunohistochemically stained sections of 100 primary SCCs divided into two groups according to diameter of the tumors (<20 mm and >20 mm) were assessed. Recombinant rabbit anti-PD-L1 antibody [SP142] - C-terminal, rabbit monoclonal anti-PD1 antibody [NAT105], and FLEX Mono Mo A-Hu CD8, cl C8/144B, RTU were used.

resultsWe did not establish statistically significant differences between PD-L1, PD-1, CD8 expression, and high-risk clinicopathological features - tumor size >20 mm, depth >6 mm, poor tumor cell differentiation, perineural/lymphovascular invasion, low/absent lymphocyte stromal reaction.

conclusionsIn primary SCCs, the expression of PD-L1, PD-1, and CD8 are not associated with high-risk clinicopathological factors. We suggest that these immunohistochemical markers are more significant in advanced cases and metastatic tissues.

Identifiers

PMID39122531
PMCPMC11313957

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