Evidence map›Paper›PMID 41149503›Full record

ReviewCurrent oncology (Toronto, Ont.)2025

Chemokine Receptors in Peripheral Blood Mononuclear Cells as Predictive Biomarkers for Immunotherapy Efficacy in Non-Small Cell Lung Cancer.

Paloma Galera, Antía Iglesias-Beiroa, Berta Hernández-Marín, Dulce Bañón, Teresa Arangoa, Lucía Castillo, María Álvarez-Maldonado, Cristina Gil-Olarte, Rafael Borregón, María Iribarren and 2 more

Abstract readReview
In one paragraph

Review in Current oncology (Toronto, Ont.), 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

12 authors.

Paloma GaleraMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Antía Iglesias-BeiroaMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Berta Hernández-MarínMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Dulce BañónMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Teresa ArangoaMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Lucía CastilloMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
María Álvarez-MaldonadoMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Cristina Gil-OlarteMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Rafael BorregónMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
María IribarrenMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.
Ramon ColomerMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.ORCID 0000-0002-6393-3444
Jacobo RogadoMedical Oncology Department, Hospital Universitario de La Princesa, Diego de León 62, 28006 Madrid, Spain.ORCID 0000-0002-9795-8762

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality globally. The advent of immune checkpoint inhibitors (ICIs) has significantly improved outcomes for a subset of patients; however, predictive biomarkers to identify responders are still lacking. Peripheral blood mononuclear cells (PBMCs) offer a minimally invasive means to assess systemic immune status and have emerged as a potential source of predictive biomarkers. Recent studies have highlighted the role of chemokines and their receptors in modulating immune responses against tumors. In particular, the expression levels of chemokine receptors such as CXCR4 on PBMCs have been associated with patient responses to ICIs. The differences in expression of these receptors correlates with enhanced T cell trafficking and infiltration into the tumor microenvironment, leading to improved antitumor activity. This review consolidates current evidence on the prognostic and predictive value of chemokine receptor expression in PBMCs, like T cells, for NSCLC patients treated with ICIs. Understanding these associations can aid in the development of non-invasive biomarkers to guide treatment decisions and improve patient stratification in immunotherapy.

Indexed as

Biomarkers, TumorCarcinoma, Non-Small-Cell LungImmunotherapyLeukocytes, MononuclearLung NeoplasmsReceptors, ChemokineHumansBiomarkers, TumorReceptors, ChemokineCCR5chemokine receptorsCXCR3CXCR4CXCR6immune checkpoint inhibitorsimmunotherapynon-small cell lung cancerpredictive biomarkers

Identifiers

PMID41149503
PMCPMC12562590

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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.