Evidence map›Paper›PMID 40778981›Full record

ArticleOncoimmunology2025

Association of PD-1, LAG-3 and TIM-3 expression on intratumoral CD8 T-cells with response to atezolizumab in a Real-World-Evidence biomarker study for advanced urothelial carcinoma patients.

Carlos E de Andrea, Marta Abengozar-Muela, José Ángel Arranz, Miguel Angel Climent, Javier Puente, Ángel Vizcay, Ligia Montero de la Fuente, José Miguel Jurado, Teresa Bonfill, Carmen Santander and 12 more

Abstract read
In one paragraph

Article in Oncoimmunology, 2025. 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.

  1. Article
  2. Review
  3. Review
  4. 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

22 authors.

Carlos E de AndreaDepartment of Pathology, Clinica Universidad de Navarra; Department of Pathology, Anatomy and Physiology, University of Navarra; Cancer Center Universidad de Navarra; IdisNA; and CIBERONC, Pamplona, Madrid, Spain.
Marta Abengozar-MuelaDepartment of Pathology, Clinica Universidad de Navarra; Department of Pathology, Anatomy and Physiology, University of Navarra; Cancer Center Universidad de Navarra; IdisNA; and CIBERONC, Pamplona, Madrid, Spain.
José Ángel ArranzDepartment of Medical Oncology, Gregorio Marañón University Hospital, Madrid, Spain.
Miguel Angel ClimentDepartment of Medical Oncology, Valencia Institute of Oncology Foundation, Valencia, Spain.
Javier PuenteDepartment of Medical Oncology, San Carlos Clinic University Hospital, Madrid, Spain.
Ángel VizcayDepartment of Oncology, CUN, CCUN and IdisNA, University of Navarra, Pamplona, Spain.
Ligia Montero de la FuenteDepartment of Oncology, CUN, CCUN and IdisNA, University of Navarra, Pamplona, Spain.
José Miguel JuradoDepartment of Oncology, San Cecilio University Hospital, Granada, Spain.
Teresa BonfillDepartment of Oncology, Parc Taulí University Hospital, Sabadell, Spain.
Carmen SantanderDepartment of Oncology, Miguel Servet Hospital, Zaragoza, Spain.
José Carlos VillaDepartment of Oncology, Ciudad Real General University Hospital, Ciudad Real, Spain.
Eduardo PujolDepartment of Oncology, Lozano Blesa Clinic University Hospital, Zaragoza, Spain.
Adriana Carolina RoseroDepartment of Medical Oncology, Infanta Cristina University Hospital, Madrid, Spain.
Jenifer GomezDepartment of Medical Oncology, Fundación Onkologikoa, Donostia-San Sebastián, Spain.
Eva María FernándezDepartment of Medical Oncology, Virgen del Valme University Hospital, Sevilla, Spain.
Carlos Álvarez FernándezDepartment of Medical Oncology, Central de Asturias University Hospital, Oviedo, Spain.
Ignacio RamirezMedical Department, Roche Farma S.A, Madrid, Spain.
Pablo ArnáizMedical Department, Roche Farma S.A, Madrid, Spain.
Álvaro López-JaneiroDepartment of Pathology, Clinica Universidad de Navarra; Department of Pathology, Anatomy and Physiology, University of Navarra; Cancer Center Universidad de Navarra; IdisNA; and CIBERONC, Pamplona, Madrid, Spain.
Ignacio MeleroDivision of Immunology and Immunotherapy, CIMA; Department of Immunology, Clinica Universidad de Navarra; Cancer Center Universidad de Navarra; IdisNA; and CIBERONC, Pamplona, Madrid, Spain.ORCID 0000-0002-1360-348X
Miguel F SanmamedDepartment of Oncology, Clinica Universidad de Navarra; Cancer Center Universidad de Navarra; IdisNA; and CIBERONC, Pamplona, Madrid, Spain.
José Luis Pérez-GraciaDepartment of Oncology, Clinica Universidad de Navarra, Cancer Center Universidad de Navarra, Pamplona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blockade of the PD-1/PD-L1 pathway is part of the standard treatment for advanced urothelial cancer, but reliable predictive biomarkers have not been identified. Here, we analyze with Multiplexed Quantitative Immunofluorescence the pretreatment tumor microenvironment (TME) of urothelial cancer samples from patients treated with atezolizumab to identify correlations with treatment efficacy in a Real-World-Evidence (RWE) study. We assessed with Multiplexed Quantitative Immunofluorescence the expression of CD8, PD-1, TIM-3 and LAG-3 on T-cells in the different compartments of the TME (tumor, stroma and whole tissue) in pre-treatment tissue microarrays. We studied associations between the expression of the markers and clinical efficacy. One hundred-nine patients received atezolizumab, showing an overall response rate of 23.8%. Safety was comparable to previous studies with atezolizumab. Pre-treatment tumor samples were available from 45 patients. CD8+ T-cell density was significantly increased in the tumor compartment, but not in the stromal compartment, of patients experiencing complete and partial responses, as compared with patients presenting stable disease or progression. Similar results were observed for co-expression of CD8/PD-1, CD8/TIM-3 and CD8/PD-1/TIM-3/LAG-3. Our findings support the relevance of the density and spatial distribution of CD8+ T-cells and its co-receptors for the clinical efficacy of single-agent PD-L1 blockade in patients with advanced urothelial cancer. RWE studies are a valuable tool for identifying predictive biomarkers.

Indexed as

Antibodies, Monoclonal, HumanizedAntigens, CDBiomarkers, TumorCD8-Positive T-LymphocytesHepatitis A Virus Cellular Receptor 2Programmed Cell Death 1 ReceptorUrinary Bladder NeoplasmsAdultAgedAged, 80 and overFemaleHumansLymphocyte Activation Gene 3 ProteinMaleMiddle AgedTumor MicroenvironmentAntibodies, Monoclonal, HumanizedAntigens, CDatezolizumabBiomarkers, TumorHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2Lag3 protein, humanLymphocyte Activation Gene 3 ProteinPDCD1 protein, humanProgrammed Cell Death 1 ReceptorAdvanced urothelial carcinomaCD8 T cellLAG-3PD-1TIM-3

Identifiers

PMID40778981
PMCPMC12952735

What OpenQuestion holds

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LicenceCC BY-NC
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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.