Evidence map›Paper›PMID 31989260›Full record

ArticleVirchows Archiv : an international journal of pathology2020

Association between PD-L1 expression and driver gene mutations in non-small cell lung cancer patients: correlation with clinical data.

Eleni A Karatrasoglou, Ilenia Chatziandreou, Stratigoula Sakellariou, Konstantinos Stamopoulos, Nikolaos Kavantzas, Andreas C Lazaris, Penelope Korkolopoulou, Angelica A Saetta

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. SHP-2 Expression Is a Positive Prognostic Biomarker in Non-Small-Cell Lung Carcinoma: Association with KRAS Mutation and Prolonged Survival.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Article
  2. PD-L1 expression scoring using artificial intelligence algorithms in non-small cell lung cancer harbouring ROS1 fusions: potential clinical-biological significance.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  15. Cancers · 2022
    Article
  16. FDA Approval Summary: Sotorasib for KRAS G12C-Mutated Metastatic NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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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

8 authors at 2 institutions in 1 country.

Eleni A Karatrasoglou *First Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece. elina_karat@hotmail.com.ORCID http://orcid.org/0000-0002-9332-6346
Ilenia Chatziandreou *First Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.
Stratigoula Sakellariou *First Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.
Konstantinos Stamopoulos *Agii Anargiri General Oncological Hospital of Kifissia, Kifisia, Greece.
Nikolaos KavantzasFirst Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.
Andreas C LazarisFirst Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.
Penelope KorkolopoulouFirst Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.
Angelica A SaettaFirst Department of Pathology, National and Kapodistrian University of Athens, Athens, Greece.
National and Kapodistrian University of Athens · GRHospital Agioi Anargyroi · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer death worldwide. Recently, promising therapies have emerged based on PD-1/PD-L1 immune checkpoint inhibitors, which have been approved even as frontline treatment for patients with non-small cell lung cancer (NSCLC). We examined the association between PD-L1 expression and clinicopathological parameters as well as overall survival in 220 NSCLC patients. PD-L1 expression was estimated by immunohistochemistry using 22C3 PharmDx Dako assay and was defined as high, if TPS was ≥ 50%, low, if TPS was 1%-49%, and absent, if TPS was < 1%. EGFR mutations were detected by COBAS while KRAS and BRAF mutations by pyrosequencing. ROS1 and ALK rearrangements were estimated by immunohistochemistry with positive cases being confirmed by CISH and FISH, respectively. Data analysis was performed using SPSS v25.0. PD-L1 expression was positively correlated with KRAS mutations. Anti-PD-1 therapy (pembrolizumab) prolonged overall survival compared to any other treatment. This effect was more pronounced in KRAS-mutated cases compared to KRAS wild-type ones. Patients with positive PD-L1 expression - high or low - who had been treated with pembrolizumab, showed significant survival benefit compared to positive or negative PD-L1 expressors who did not receive immunotherapy. In multivariate analysis, PD-L1 status, stage and pembrolizumab treatment were independent variables for overall survival. PD-L1 expression (TPS ≥ 1%) by itself emerged as a poor prognostic factor, while treatment with pembrolizumab prolonged overall survival. KRAS mutations may affect tumour microenvironment and patient's response to immunotherapy. Immune checkpoint inhibitors could represent an alternative therapeutic option particularly for KRAS-mutated NSCLC patients. Further investigation into this notion is warranted in order to validate this observation.

Indexed as

AdultAnaplastic Lymphoma KinaseAntibodies, Monoclonal, HumanizedB7-H1 AntigenBiomarkers, TumorCarcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsMaleMiddle AgedMutationProtein-Tyrosine KinasesTumor MicroenvironmentAnaplastic Lymphoma KinaseAntibodies, Monoclonal, HumanizedB7-H1 AntigenBiomarkers, TumorCD274 protein, humanpembrolizumabProtein-Tyrosine KinasesKRASNon-small cell lung cancer (NSCLC)PembrolizumabProgrammed cell death ligand 1 (PD-L1)

Identifiers

PMID31989260
OpenAlexW3003015741

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.