Evidence map›Paper›PMID 41933080›Full record

ArticleNPJ digital medicine2026

Label-free pathological subtyping of non-small cell lung cancer using deep classification and virtual immunohistochemical staining.

Zhenya Zang, David A Dorward, Katherine E Quiohilag, Andrew Dj Wood, James R Hopgood, Ahsan R Akram, Qiang Wang

Abstract read
In one paragraph

Article in NPJ digital medicine, 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

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. 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

7 authors.

Zhenya ZangCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK.
David A DorwardDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
Katherine E QuiohilagDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
Andrew Dj WoodDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
James R HopgoodInstitue of Imaging, Data and Communications, School of Engineering, The University of Edinburgh, Edinburgh, UK.
Ahsan R AkramCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK. Ahsan.Akram@ed.ac.uk.
Qiang WangCentre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, UK. Q.Wang@ed.ac.uk.

Funding

Engineering and Physical Sciences Research Council EP/S025987/1UKRI Future Leaders Fellowship MR/Y015460/1UoE Medical Research Council and Harmonised Impact Acceleraor Accounts awards MRC/IAA/015 and HIAA/037UoE Wellcome Institutional Translational Partnership Accelerator Fund and Cancer Research Horizons Seed Fund PIII140
6 · The paper itself

Abstract

The differentiation between pathological subtypes of non-small cell lung cancer (NSCLC) is an essential step in guiding treatment options and prognosis. However, current clinical practice relies on multi-step staining and labelling processes that are time-intensive and costly, requiring highly specialised expertise. In this study, we propose a label-free methodology that facilitates autofluorescence imaging of unstained NSCLC samples and deep learning (DL) techniques to distinguish between non-cancerous tissue, adenocarcinoma (AC), squamous cell carcinoma (SqCC), and other subtypes (OS). We conducted DL-based classification and generated virtual immunohistochemical (IHC) stains, including thyroid transcription factor-1 (TTF-1) for AC and p40 for SqCC. We evaluated these methods using two types of autofluorescence imaging: intensity imaging and lifetime imaging. The results demonstrate the exceptional ability of this approach for NSCLC subtype differentiation, achieving an area under the curve above 0.981 and 0.996 for binary- and multi-class classification. Furthermore, this approach produces clinical-grade virtual IHC staining, which was blind-evaluated by three experienced thoracic pathologists. Our label-free NSCLC subtyping approach enables rapid and accurate diagnosis without the need for conventional tissue processing and staining. Both strategies can significantly accelerate diagnostic workflows and support efficient lung cancer diagnosis, without compromising clinical decision-making.

Identifiers

PMID41933080
PMCPMC13249941

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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.