Evidence map›Paper›PMID 41240064›Full record

ArticleThe Journal of pathology2026

Novel growth pattern-specific digital marker of TILs improves stratification of lung adenocarcinoma patients.

Arwa AlRubaian, Ayesha Azam, Nasir M Rajpoot, Shan E Ahmed Raza

Abstract read
In one paragraph

Article in The Journal of pathology, 2026. 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

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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

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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

4 authors.

Arwa AlRubaianTissue Image Analytics Centre, Department of Computer Science, University of Warwick, Coventry, UK.ORCID https://orcid.org/0000-0002-5905-6602
Ayesha AzamDepartment of Cellular Pathology, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
Nasir M RajpootTissue Image Analytics Centre, Department of Computer Science, University of Warwick, Coventry, UK.
Shan E Ahmed RazaTissue Image Analytics Centre, Department of Computer Science, University of Warwick, Coventry, UK.

Funding

European Commission 945358GlaxoSmithKlineSaudi Cultural Bureau in London
6 · The paper itself

Abstract

Lung adenocarcinoma (LUAD) is one of the most prevalent forms of cancer and continues to be associated with high mortality rates, despite recent advances in cancer therapy. Effective risk stratification is critical for guiding treatment decisions and improving our understanding of disease mechanisms. However, current prognostic approaches face considerable limitations. Growth pattern-based grading serves as a prognostic indicator of tumour aggressiveness, but is inherently subjective and prone to a high degree of variability among observers. Other well-established prognostic indicators, such as tumour infiltrating lymphocytes (TILs) and stromal TILs (sTILs) scores, provide valuable prognostic information but require labour-intensive assessment. The pronounced heterogeneity of LUAD further complicates prognosis and underscores the need for robust, integrative biomarkers that capture both the morphological and immunological characteristics of the tumour. To address this need, we propose an AI-based growth-pattern-specific TILs (GPS-TILs) marker that quantifies TILs and sTILs within each growth pattern separately. By integrating morphological information from the tumour growth patterns and immune microenvironment data from TILs, we demonstrate that the proposed GPS-TILs marker improves patient stratification. We evaluated the prognostic utility of GPS-TILs using survival analysis with Cox proportional hazards models in a cross-validation setting using The Cancer Genome Atlas LUAD (TCGA-LUAD) cohort. Our findings revealed that GPS-TILs offers strong prognostic value for overall survival (p < 0.0001, C-index = 0.59), outperforming conventional TIL-based measures and morphology-based stratification approaches. These results highlight the potential of GPS-TILs as a more objective and effective tool for improving patient risk stratification in LUAD. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Adenocarcinoma of LungBiomarkers, TumorLung NeoplasmsLymphocytes, Tumor-InfiltratingAgedFemaleHumansMaleMiddle AgedPrognosisTumor MicroenvironmentBiomarkers, Tumorartificial intelligencehistological growth patternshistology imageslung adenocarcinomalymphocytesSTILssurvival analysisTILstumour microenvironment

Identifiers

PMID41240064
PMCPMC12805620

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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.