Evidence map›Paper›PMID 40673081›Full record

ArticleTranslational lung cancer research2025

Enhancing the intraoperative identification of high-grade patterns in invasive lung adenocarcinoma via radiomics.

Yuanxin Sun, Hao Dong, Weiqiu Jin, Haoxiang Xuan, Zheng Yuan, Lukas Käsmann, Leilei Shen, Tingting Wang, Xiaodan Ye, Mengsu Zeng

Abstract read
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Article in Translational lung cancer research, 2025. 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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5 · Who and what money

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10 authors.

Yuanxin Sun *Shanghai Institute of Medical Imaging, Shanghai, China.ORCID https://orcid.org/0009-0000-3896-0427
Hao Dong *Department of Radiology, First People's Hospital of Xiaoshan District, Hangzhou, China.
Weiqiu Jin *Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Haoxiang XuanDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zheng YuanDepartment of Radiology, Shanghai Ninth Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Lukas KäsmannDepartment of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.
Leilei ShenDepartment of Radiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Tingting WangDepartment of Radiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xiaodan YeShanghai Institute of Medical Imaging, Shanghai, China.ORCID https://orcid.org/0000-0003-3059-2740
Mengsu ZengShanghai Institute of Medical Imaging, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: High-grade patterns (HGPs) are important for surgical decision-making in patients with invasive lung adenocarcinoma (IAC), but the sensitivity of intraoperative frozen section (FS) is not high. Radiomics has the potential to improve the sensitivity of intraoperative detection. The purpose of the present study was to evaluate the value of combining radiomics with FS analysis for predicting HGPs in patients with clinical T1 (cT1) IAC. Methods: Data from a total of 490 patients who were surgically diagnosed with IAC from January 2019 to April 2019 were retrospectively analyzed; the patients were randomly divided into a training set (n=392) and a test set (n=98). The presence of HGPs (micropapillary, solid, and complex glandular patterns) was evaluated according to the final pathology (FP). Radiomics features were extracted from thin-slice computed tomography (CT) images, and feature selection was performed via the mutual information method and least absolute shrinkage and selection operator regression algorithm. The radiomics (R), FS, and radiomics-frozen section (R-FS) models were established to predict the presence of HGPs in FP. The area under the receiver operating characteristic (ROC) curve, the precision-recall curve, the calibration curve, and decision curve analysis were used to evaluate model performances. The permutation importance algorithm (PIA) and local interpretable model-agnostic explanations (LIME) were used to provide interpretations for the R model. Additionally, the predictive performance was compared among tumors with different CT densities. Results: The R and R-FS models outperformed the FS model, with the R-FS model achieving the best area under the curve value of 0.907 (95% confidence interval: 0.830-0.956) in the test set. PIA and LIME determined the interpretability of outputs from both the overall model and individual sample perspectives. Among the three models, the R model performed best in pure ground-glass nodules and pure-solid tumors. Conclusions: Radiomics could function as a complementary check to FS to provide a more sensible and accurate intraoperative identification of HGPs as compared to the use of FS alone, thus better informing clinical decision-making.

Indexed as

frozen section (FS)high-grade pattern (HGP)lung adenocarcinoma (LUAD)machine learningnon-high-grade pattern (non-HGP)Radiomics

Identifiers

PMID40673081
PMCPMC12261232

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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.