Evidence map›Paper›PMID 40650126›Full record

ArticleInternational journal of molecular sciences2025

PD-L1 Expression and Comprehensive Genomic Profiling in Advanced NSCLC: A Single-Centre Experience.

Giedrė Gurevičienė, Lina Poškienė, Skaidrius Miliauskas, Marius Žemaitis

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. COPD-Lung Cancer Comorbidity: Mechanistic Insights and Precision Oncology Implications.International journal of chronic obstructive pulmonary disease · 2026
    Review
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

4 authors.

Giedrė GurevičienėDepartment of Pulmonology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.
Lina PoškienėDepartment of Pathology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.
Skaidrius MiliauskasDepartment of Pulmonology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.ORCID 0009-0002-6130-0712
Marius ŽemaitisDepartment of Pulmonology, Medical Academy, Lithuanian University of Health Sciences, 44307 Kaunas, Lithuania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although immunotherapy has led to a breakthrough in the treatment of NSCLC, fast disease progression in some patients remains problematic. Great efforts are being made to identify the mechanisms of immune resistance and to establish new predictive and prognostic biomarkers. The aim of this study was to evaluate the association between PD-L1 expression, genetic alterations, and prognosis in patients diagnosed with metastatic NSCLC. PD-L1 expression and genetic profiling using NGS were assessed in 50 patients with advanced NSCLC who were negative for EGFR mutations. According to this study results, positive PD-L1 expression was detected in 62% of cases, whereas high TMB was detected in 34% of cases. Targetable mutations were detected in 33.4% of cases. The TP53 mutation was more likely to be found in tumours with higher PD-L1 and TMB levels (median 45 vs. 0,

Indexed as

B7-H1 AntigenCarcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedAged, 80 and overAMP-Activated Protein Kinase KinasesBiomarkers, TumorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunotherapyKelch-Like ECH-Associated Protein 1MaleMiddle AgedAMP-Activated Protein Kinase KinasesB7-H1 AntigenBiomarkers, TumorCD274 protein, humanKEAP1 protein, humanKelch-Like ECH-Associated Protein 1Protein Serine-Threonine KinasesSTK11 protein, humanTumor Suppressor Protein p53fast disease progressiongenetic profilingKEAP1non-small cell lung cancerprogrammed death-ligand 1STK11TP53tumour mutation burden

Identifiers

PMID40650126
PMCPMC12249841

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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.