ReviewJournal of translational medicine2025
Applications of artificial intelligence in non-small cell lung cancer: from precision diagnosis to personalized prognosis and therapy.
Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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.
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.
Who cites it
5 citing papers in PubMed.
- Radiomics: Current Applications and Future Directions.MedComm · 2026Review
- Exosomal circPOLK promotes metastasis of NSCLC cells via regulating mir-1204/SOX8 axis.Cancer cell international · 2026Article
- Application of deep learning in prognostic prediction of non-small cell lung cancer.Frontiers in cell and developmental biology · 2026Review
- Artificial intelligence in non-small cell lung cancer: transforming diagnosis, treatment, and prognostic evaluation.Frontiers in medicine · 2026Review
- Generative artificial intelligence in lung cancer care: current applications, challenges, and future directions.Frontiers in oncology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundNon-small cell lung cancer (NSCLC) carries a major global burden. The rapid growth of multimodal medical data challenges conventional methods to deliver stable, transferable and interpretable decisions across heterogeneous longitudinal high dimensional inputs.
methodsThis review summarizes advances in artificial intelligence (AI) for NSCLC from 2023 to 2025 and outlines a translation-focused framework that links algorithmic progress to clinical utility. We survey thoracic imaging, digital pathology and multiomics together with evaluation practices and implementation guidance. We also adopt a critical perspective.
resultsMany high performing deep models remain black boxes, and popular post hoc explanations such as Grad CAM heatmaps are rarely validated for faithfulness or stability, which undermines clinician trust and limits use in high stakes decisions. To address this gap, we propose a minimum evidence package for explainability that comprises sanity checks, quantitative faithfulness tests such as deletion or insertion, ROAR or IROF and infidelity, stability analyses, concept level validation for example TCAV with statistical testing, and prospective human factors studies that demonstrate improved decisions without automation bias. Across modalities, evaluation has expanded beyond discrimination to include calibration, uncertainty quantification (UQ) and subgroup analyses across scanners, sites and populations. However, the evidence base remains constrained by retrospective single center designs, inconsistent external or temporal validation and limited decision curve analysis (DCA). Translational priorities include a staged validation ladder from technical to clinical to prospective deployment, alignment with Software as a Medical Device frameworks, interoperable governance, fairness and economic assessment, and validated explainability coupled with uncertainty aware selective workflows.
conclusionsLooking ahead, progress will depend on multimodal foundation models, causal and temporal modeling, and regulatory qualification of computable biomarkers with verified explanations, supported by multicenter prospective studies that demonstrate durable generalizability, clinical value and clinician trust.
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Registered trials
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.