Evidence map›Paper›PMID 38793038›Full record

ArticleJournal of personalized medicine2024

Prognostic Value of KRAS Mutations in Relation to PDL1 Expression and Immunotherapy Treatment in Adenocarcinoma and Squamous Cell Carcinoma Patients: A Greek Cohort Study.

Theodora Tsiouda, Kalliopi Domvri, Efimia Boutsikou, Vasileios Bikos, Krystallia Kyrka, Konstantina Papadaki, Persefoni Pezirkianidou, Konstantinos Porpodis, Angeliki Cheva

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Article in Journal of personalized medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

9 authors.

Theodora TsioudaPulmonary-Oncology Department, 'Theageneio' Cancer Hospital, 540 07 Thessaloniki, Greece.
Kalliopi DomvriLaboratory of Histology-Embryology, Medical School, Aristotle University, 541 24 Thessaloniki, Greece.ORCID 0000-0002-4812-9108
Efimia BoutsikouPulmonary-Oncology Department, 'Theageneio' Cancer Hospital, 540 07 Thessaloniki, Greece.
Vasileios BikosPulmonary-Oncology Department, 'Theageneio' Cancer Hospital, 540 07 Thessaloniki, Greece.
Krystallia KyrkaPulmonary-Oncology Department, 'Theageneio' Cancer Hospital, 540 07 Thessaloniki, Greece.
Konstantina PapadakiPulmonary-Oncology Department, 'Theageneio' Cancer Hospital, 540 07 Thessaloniki, Greece.
Persefoni PezirkianidouPulmonary-Oncology Department, 'Theageneio' Cancer Hospital, 540 07 Thessaloniki, Greece.
Konstantinos PorpodisPulmonary Department, Medical School, Aristotle University of Thessaloniki, "G. Papanikolaou" General Hospital, Exohi, 570 10 Thessaloniki, Greece.
Angeliki ChevaDepartment of Pathology, AHEPA University Hospital of Thessaloniki, Aristotle University, 541 24 Thessaloniki, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFactors that could predict which patients will benefit from Immune Checkpoint Inhibitors (ICIs) are not fully understood. This study aimed to investigate the prognostic value of KRAS biomarker in patients with advanced non-small cell lung cancer (NSCLC) in relation to clinical characteristics, treatment response and PDL1 expression. PATIENTS AND

methodsThe study included 100 patients with NSCLC who received immunotherapy with or without chemotherapy as 1st line treatment. In biopsy samples, the PDL1 biomarker expression rate and somatic mutations of KRAS gene were determined.

resultsThe mean age of the patients was 67 ± 8 years. Patients were all male and 66% were found with adenocarcinoma whereas 34% with squamous cell carcinoma. The KRAS G12C mutation was found with the highest percentage (73%). In the Kaplan-Meier survival analysis, patients with PDL1 > 49% in combination with a negative KRAS result had a median overall survival of 40 months compared to patients with a positive KRAS result (9 months,

conclusionsOur study suggests that the presence of KRAS mutations in advanced NSCLC patients has a poor prognostic value, regardless of their PDL1 expression values, after receiving immunotherapy as first-line treatment.

Indexed as

immunotherapyKRASlung cancerPDL1survival

Identifiers

PMID38793038
PMCPMC11121847

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