Evidence map›Paper›PMID 41266384›Full record

ArticleScientific reports2025

Tissue and peripheral T cell receptor repertoire predicts immunotherapy response and progression-free survival in NSCLC patients.

Manuel Pino-González, Martín Lázaro-Quintela, Irene Alonso-Álvarez, María Gallardo-Gómez, Laura Juaneda-Magdalena, Alejandro Francisco-Fernández, Silvia Calabuig-Fariñas, Eloisa Jantus-Lewintre, Mónica Martínez-Fernández

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
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.

  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

9 authors.

Manuel Pino-González *Translational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain.
Martín Lázaro-Quintela *Translational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain.
Irene Alonso-ÁlvarezTranslational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain.
María Gallardo-GómezTranslational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain.
Laura Juaneda-MagdalenaTranslational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain.
Alejandro Francisco-FernándezTranslational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain.
Silvia Calabuig-FariñasDepartment of Pathology, Universitat de València, 46010, Valencia, Spain.
Eloisa Jantus-LewintreCentro de Investigación Biomédica en Red Cáncer (CIBERONC), Valencia, Spain.
Mónica Martínez-FernándezTranslational Oncology Group, Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO, Hospital Álvaro Cunqueiro, Carretera Clara Campoamor, 341, 36213, Vigo, Spain. monica.martinez@iisgaliciasur.es.

Funding

Axencia Galega de Innovación IN606A-2024/017Axencia Galega de Innovación IN606B-2024/014European Social Fund Plus CP20/00188Instituto de Salud Carlos III PI21/00348Ministerio de Ciencia, Innovación y Universidaders FPU23/00744
6 · The paper itself

Abstract

Immunotherapy has opened new avenues of treatment for patients with advanced non-small cell lung cancer (NSCLC) without previous hope of survival. Unfortunately, only a small percentage of patients benefit from it and there is not an effective biomarker to predict patients' response. Since T cells are key effectors of antitumor immunity, T cell receptor (TCR) has emerged as a potential predictive biomarker. Here, we evaluated the potential of baseline TCR repertoire, as a predictive biomarker in advanced NSCLC patients treated with pembrolizumab at first-line. After obtaining peripheral blood and tissue samples at baseline, next-generation sequencing targeting TCRβ/γ was performed. We found an uneven tumor-infiltrating TCRβ repertoire, and the use of various tumor-infiltrating and circulating TRBV/J genes were able of predicting the immunotherapy response. Our results support the potential of evaluating tissue and circulating TCRβ repertoire prior to pembrolizumab, revealing it as a promising immunotherapy response biomarker in NSCLC patients.

Indexed as

Carcinoma, Non-Small-Cell LungImmunotherapyLung NeoplasmsReceptors, Antigen, T-CellAgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBiomarkers, TumorFemaleHumansLymphocytes, Tumor-InfiltratingMaleMiddle AgedProgression-Free SurvivalReceptors, Antigen, T-Cell, alpha-betaAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalBiomarkers, TumorpembrolizumabReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaImmunotherapy responseNon-small cell lung cancerPembrolizumabPredictive biomarkerT cell receptorTCR repertoire

Identifiers

PMID41266384
PMCPMC12635383

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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.