Evidence map›Paper›PMID 41572744›Full record

ArticleCurrent medical imaging2026

The Predictive Value of

Min Tang, Chunlei Zhao, Shengwei Fang

Abstract read
In one paragraph

Article in Current medical imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Min TangDepartment of Radiology, Wuhan No. 1 Hospital, Wuhan, 430022, China.
Chunlei ZhaoDepartment of Nuclear Medicine, Hangzhou Cancer Hospital, Hangzhou310002, China.
Shengwei FangDepartment of Nuclear Medicine, Hangzhou Cancer Hospital, Hangzhou310002, China.ORCID 0009-0005-9785-7565

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis study aimed to evaluate the predictive value of radiomic features derived from 18F-FluoroDeoxyGlucose (FDG) PET/CT for Epidermal Growth Factor Receptor (EGFR) gene mutations in patients with lung adenocarcinoma.

methodsA retrospective analysis was conducted on 93 patients diagnosed with solitary lung adenocarcinoma who underwent 18F-FDG PET/ CT imaging and EGFR mutation results. The patients were divided into training (46 cases) and testing (47 cases) cohorts. Radiomic features were extracted from the primary tumor sites' PET and CT images. Feature selection was performed using the Mann-Whitney U test and least absolute shrinkage and selection operator (LASSO) regression. A radiomics score (Rad-score) was constructed, and combined models incorporating clinical factors and metabolic parameters were developed. Predictive performance was evaluated using receiver operating characteristic (ROC) curves, area under the curve (AUC), accuracy, and decision curve analysis (DCA).

resultsThe radiomics model achieved AUCs of 0.865 (95% CI: 0.747-0.983) and 0.737 (95% CI: 0.572-0.901) in the training and testing sets, respectively, with corresponding accuracies of 80.9% and 78.3%. The clinical model alone demonstrated inferior performance, with AUCs of 0.637 and 0.645. The combined model showed slightly improved AUCs (0.885 and 0.714) but did not significantly outperform the radiomics-only model (P > 0.05). DCA indicated greater clinical utility for the radiomics model across a wide range of threshold probabilities. DISCUSSION: PET/CT-based radiomics research has also achieved good efficacy in predicting EGFR gene mutations. Compared with morphological imaging techniques, such as X-ray, ultrasound, and CT, 18F-FDG PET/CT imaging has the significant advantage of providing functional and metabolic information of lesions. Both radiomics and composite models could predict EGFR mutation status in lung adenocarcinoma patients, but the radiomics model showed slightly better clinical predictive efficacy than the composite model.

conclusionThe radiomics model and the combined model integrating Rad-score with clinical factors demonstrated comparable abilities in effectively predicting EGFR mutation status in patients with lung adenocarcinoma. These models could offer a non-invasive approach for identifying EGFR mutations.

Indexed as

Adenocarcinoma of LungLung NeoplasmsPositron Emission Tomography Computed TomographyAgedErbB ReceptorsFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedMutationPredictive Value of TestsRadiomicsRadiopharmaceuticalsRetrospective StudiesEGFR protein, humanErbB ReceptorsFluorodeoxyglucose F18Radiopharmaceuticals18F-FDGEpidermal Growth Factor ReceptorLung AdenocarcinomaPET/CTPrediction.Radiomics

Identifiers

PMID41572744
PMCPMC13312375

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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.