ArticleNPJ digital medicine2026
Label-free pathological subtyping of non-small cell lung cancer using deep classification and virtual immunohistochemical staining.
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.
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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.
The trial behind it
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Who cites it
1 citing paper in PubMed.
- Artificial intelligence in non-small cell lung cancer: transforming diagnosis, treatment, and prognostic evaluation.Frontiers in medicine · 2026Review
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Authors and funding
7 authors.
Funding
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.
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Registered trials
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