Evidence map›Paper›PMID 38545362›Full record

ArticleTurk gogus kalp damar cerrahisi dergisi2024

The prognostic significance of PD-1 and its ligands in non-small cell lung cancer.

Ozan Usluer, Özde Elif Gökbayrak, Aylin Erol, Tekincan Çağrı Aktaş, Güntuğ Batıhan, Şeyda Örs Kaya, Ahmet Üçvet, Zekiye Aydoğdu, Zekiye Altun, İlhan Öztop and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Turk gogus kalp damar cerrahisi dergisi, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 97% of its field
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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Article
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

11 authors at 3 institutions in 2 countries.

Ozan UsluerDepartment of Thoracic Surgery, University of Health Sciences, Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital, Izmir, Türkiye.ORCID 0000-0002-5272-3310
Özde Elif GökbayrakDepartment of Basic Oncology, Dokuz Eylül University, Institute of Health Sciences, Izmir, Türkiye.ORCID 0000-0002-8765-0641
Aylin ErolDepartment of Basic Oncology, Dokuz Eylül University, Institute of Health Sciences, Izmir, Türkiye.ORCID 0000-0002-1019-0026
Tekincan Çağrı AktaşDepartment of Basic Oncology, Dokuz Eylül University, Institute of Health Sciences, Izmir, Türkiye.ORCID 0000-0002-4960-5225
Güntuğ BatıhanDepartment of Thoracic Surgery, Kars Harakani State Hospital, Kars, Türkiye.ORCID 0000-0001-5258-2856
Şeyda Örs KayaDepartment of Thoracic Surgery, University of Health Sciences, Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital, Izmir, Türkiye.ORCID 0000-0002-0751-6240
Ahmet ÜçvetDepartment of Thoracic Surgery, University of Health Sciences, Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital, Izmir, Türkiye.ORCID 0000-0002-5649-560X
Zekiye AydoğduDepartment of Thoracic Surgery, Kars Harakani State Hospital, Kars, Türkiye.ORCID 0000-0003-1905-7050
Zekiye AltunDepartment of Basic Oncology, Dokuz Eylül University, Institute of Health Sciences, Izmir, Türkiye.ORCID 0000-0002-1558-4534
İlhan ÖztopDepartment of Pathology, University of Health Sciences, Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital, Izmir, Türkiye.ORCID 0000-0002-0425-0651
Safiye AktaşDepartment of Basic Oncology, Dokuz Eylül University, Institute of Health Sciences, Izmir, Türkiye.ORCID 0000-0002-7658-5565
Dokuz Eylül University · TRIzmir University · TRState Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In this study, we aimed to investigate the prognostic value of programmed cell death protein 1 (PD-1), programmed cell death ligand 1 (PD-L1), and programmed cell death ligand 2 (PD-L2) expressions on immune and cancer cells in terms of survival in patients with lung adenocarcinoma, squamous cell carcinoma, and large cell carcinoma. Methods: Between January 2000 and December 2012, a total of 191 patients (172 males, 19 females; mean age: 60.3±8.4 years; range, 38 to 78 years) who were diagnosed with non-small cell lung cancer and underwent anatomic resection and mediastinal lymph node dissection were retrospectively analyzed. The patients were evaluated in three groups including lung squamous cell carcinoma (n=61), adenocarcinoma (n=66), and large-cell carcinoma (n=64). The survival rates of all three groups were compared in terms of immunohistochemical expression levels of PD-1, PD-L1, and PD-L2. Results: The mean follow-up was 71.8±47.9 months. In all histological subtypes, PD-1 expressions on tumor and immune cells were observed in 33% (61/191) and in 53.1% (102/191) of the patients, respectively. Higher expression levels of PD-L1 and PD-L2 at any intensity on tumor and immune cells were defined only in lung adenocarcinomas, and PD-L1 and PD-L2 values were detected in 36.4% (22/64) of these patients. The PD-L1 expressions on tumor and immune cells were observed in 41.7% (10/24) and 25% (6/24) of the patients, respectively. The PD-L2 expressions on tumor and immune cells were detected in 16.7% (4/24) and 8.4% (2/24) of the patients, respectively. Univariate and multivariate analyses revealed that PD-1 expression in tumor cells was an independent prognostic factor in all histological subtypes. Conclusion: Our study results suggest that PD-1 expression is a poor prognostic factor for overall survival in patients with completely resected adenocarcinoma, squamous cell carcinoma, and large cell carcinoma.

Indexed as

Non-small cell lung cancerprognosisprogrammed cell death ligand 1programmed cell death ligand 2programmed cell death protein 1survival.

Identifiers

PMID38545362
PMCPMC10964310
OpenAlexW4391758938

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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.