Evidence map›Paper›PMID 40921820›Full record

SynthesisEuropean radiology2026

Prediction of oncogene mutation status in non-small cell lung cancer: a systematic review and meta-analysis with a special focus on artificial intelligence-based methods.

Almudena Fuster-Matanzo, Alfonso Picó-Peris, Fuensanta Bellvís-Bataller, Ana Jimenez-Pastor, Glen J Weiss, Luis Martí-Bonmatí, Antonio Lázaro Sánchez, David Bazaga, Giuseppe L Banna, Alfredo Addeo and 3 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
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  8. 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

13 authors.

Almudena Fuster-Matanzo *Quantitative Imaging Biomarkers in Medicine, Quibim, Valencia, Spain. almudenafuster@quibim.com.ORCID http://orcid.org/0000-0001-8667-4011
Alfonso Picó-Peris *Quantitative Imaging Biomarkers in Medicine, Quibim, Valencia, Spain.
Fuensanta Bellvís-BatallerQuantitative Imaging Biomarkers in Medicine, Quibim, Valencia, Spain.
Ana Jimenez-PastorQuantitative Imaging Biomarkers in Medicine, Quibim, Valencia, Spain.
Glen J WeissQuantitative Imaging Biomarkers in Medicine, Quibim, New York, NY, USA.
Luis Martí-BonmatíGrupo de Investigación Biomédica en Imagen, Instituto de Investigación Sanitaria La Fe, Valencia, Spain.
Antonio Lázaro SánchezDepartment of Medical Oncology, Hospital General Universitario Morales Meseguer, Murcia, Spain.
David BazagaQuantitative Imaging Biomarkers in Medicine, Quibim, Valencia, Spain.
Giuseppe L BannaDepartment of Oncology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK.
Alfredo AddeoOncology Service, University Hospital Geneva, Geneva, Switzerland.
Carlos CampsDepartment of Medicine, University of Valencia, Valencia, Spain.
Luis M SeijoClínica Universidad de Navarra, Madrid, Spain.
Ángel Alberich-BayarriQuantitative Imaging Biomarkers in Medicine, Quibim, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn non-small cell lung cancer (NSCLC), non-invasive alternatives to biopsy-dependent driver mutation analysis are needed. We reviewed the effectiveness of radiomics alone or with clinical data and assessed the performance of artificial intelligence (AI) models in predicting oncogene mutation status. MATERIALS AND

methodsA PRISMA-compliant literature review for studies predicting oncogene mutation status in NSCLC patients using radiomics was conducted by a multidisciplinary team. Meta-analyses evaluating the performance of AI-based models developed with CT-derived radiomics features alone or combined with clinical data were performed. A meta-regression to analyze the influence of different predictors was also conducted.

resultsOf 890 studies identified, 124 evaluating models for the prediction of epidermal growth factor-1 (EGFR), anaplastic lymphoma kinase (ALK), and Kirsten rat sarcoma virus (KRAS) mutations were included in the systematic review, of which 51 were meta-analyzed. The AI algorithms' sensitivity/false positive rate (FPR) in predicting mutation status using radiomics-based models was 0.754 (95% CI 0.727-0.780)/0.344 (95% CI 0.308-0.381) for EGFR, 0.754 (95% CI 0.638-0.841)/0.225 (95% CI 0.163-0.302) for ALK and 0.475 (95% CI 0.153-0.820)/0.181 (95% CI 0.054-0.461) for KRAS. A meta-analysis of combined models was possible for EGFR mutation, revealing a sensitivity of 0.806 (95% CI 0.777-0.833) and a FPR of 0.315 (95% CI 0.270-0.364). No statistically significant results were obtained in the meta-regression.

conclusionsRadiomics-based models may offer a non-invasive alternative for determining oncogene mutation status in NSCLC. Further research is required to analyze whether clinical data might boost their performance. KEY POINTS: Question Can imaging-based radiomics and artificial intelligence non-invasively predict oncogene mutation status to improve diagnosis in non-small cell lung cancer (NSCLC)? Findings Radiomics-based models achieved high performance in predicting mutation status in NSCLC; adding clinical data showed limited improvement in predictive performance. Clinical relevance Radiomics and AI tools offer a non-invasive strategy to support molecular profiling in NSCLC. Validation studies addressing clinical and methodological aspects are essential to ensure their reliability and integration into routine clinical practice.

Indexed as

Artificial IntelligenceCarcinoma, Non-Small-Cell LungLung NeoplasmsMutationOncogenesAnaplastic Lymphoma KinaseErbB ReceptorsHumansTomography, X-Ray ComputedALK protein, humanAnaplastic Lymphoma KinaseErbB ReceptorsArtificial intelligenceDiagnostic imagingMutationNon-small cell lung cancer.Radiomics

Identifiers

PMID40921820
PMCPMC12963223

What OpenQuestion holds

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Registered trials

None linked

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.