Evidence map›Paper›PMID 40725183›Full record

ArticleInternational journal of molecular sciences2025

Exploring the Impact of TP53 Mutation and Wild-Type Status on the Efficacy of Immunotherapy in Non-Small Cell Lung Cancer.

Alexander Yakobson, Ronen Brenner, Itamar Gothelf, Natalie Maimon Rabinovich, Ahron Yehonatan Cohen, Ashraf Abu Jama, Nashat Abu Yasin, Fahmi Abu Ghalion, Abed Agbarya, Walid Shalata

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. Revisiting tumor immunogenicity through the lens of mutant p53: Implications for cancer immunotherapy.Apoptosis : an international journal on programmed cell death · 2026
    Review
  2. Review
  3. 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

10 authors.

Alexander YakobsonThe Legacy Heritage Cancer Center, Dr. Larry Norton Institute, Soroka Medical Center, Beer Sheva 84105, Israel.
Ronen BrennerEdith Wolfson Medical Center, Oncology Institute, Holon 58220, Israel.
Itamar GothelfGoldman Medical School, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel.
Natalie Maimon RabinovichDepartment of Oncology, Meir Medical Center, Kfar Saba 44180, Israel.ORCID 0009-0006-7106-9306
Ahron Yehonatan CohenThe Legacy Heritage Cancer Center, Dr. Larry Norton Institute, Soroka Medical Center, Beer Sheva 84105, Israel.
Ashraf Abu JamaThe Legacy Heritage Cancer Center, Dr. Larry Norton Institute, Soroka Medical Center, Beer Sheva 84105, Israel.
Nashat Abu YasinThe Legacy Heritage Cancer Center, Dr. Larry Norton Institute, Soroka Medical Center, Beer Sheva 84105, Israel.
Fahmi Abu GhalionFaculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva 84105, Israel.ORCID 0009-0002-6840-790X
Abed AgbaryaOncology Department, Bnai Zion Medical Center, Haifa 31048, Israel.ORCID 0000-0002-3330-2959
Walid ShalataThe Legacy Heritage Cancer Center, Dr. Larry Norton Institute, Soroka Medical Center, Beer Sheva 84105, Israel.ORCID 0000-0002-7570-4550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TP (tumor protein) 53 mutation status plays a critical role in cancer progression and may influence survival outcomes in non-small cell lung cancer (NSCLC) patients receiving immunotherapy. This study investigates the impact of TP53 mutation status and immunotherapy treatment on survival in NSCLC patients. This retrospective study analyzed NSCLC patients treated with pembrolizumab or ipilimumab plus nivolumab, stratified by TP53 mutation status and PD-L1 (programmed death-ligand 1) expression (<1%, 1-49%, >50%). Survival outcomes (overall survival (OS) and progression free survival (PFS) were assessed using Kaplan-Meier curves and log-rank tests, with subgroup analysis by histological subtype. In squamous cell cancer (SCC) patients, no significant differences in OS or PFS were found based on TP53 mutation status or treatment type. A trend toward improved survival was observed with pembrolizumab (

Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsMutationTumor Suppressor Protein p53AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedB7-H1 AntigenFemaleHumansIpilimumabKaplan-Meier EstimateMaleMiddle AgedAntibodies, Monoclonal, HumanizedB7-H1 AntigenCD274 protein, humanIpilimumabNivolumabpembrolizumabTP53 protein, humanTumor Suppressor Protein p53immunotherapylung cancerNSCLCreal-world evidencetumor protein P53 (TP53)

Identifiers

PMID40725183
PMCPMC12296095

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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.