Evidence map›Paper›PMID 40061892›Full record

ArticleFrontiers in oncology2025

Combining clinical characteristics with CT radiomics to predict Ki67 expression level of small renal mass based on artificial intelligence algorithms.

Junyi Lin, Yongyi Ou, Mingli Luo, Xuxuan Jiang, Shengren Cen, Guohua Zeng

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Junyi Lin *Department of Urology, The First Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Yongyi Ou *Department of Urology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Mingli Luo *Department of Urology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Xuxuan JiangDepartment of Ophthalmology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Shengren CenDepartment of Urology, The First Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Guohua ZengDepartment of Urology, The First Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Most small renal masses (SRMs) grow slowly and have good prognosis, but a portion of SRMs can also demonstrate aggressive characteristics, which can be explored by the proliferation-related marker Ki67. Methods: A total of 241 patients collected from the two centers were included in the study, of which 145 patients from the First Affiliated Hospital of Guangzhou Medical University were divided into training and validation cohort, while 96 patients from Sun Yat-sen Memorial Hospital were served as test cohort. To ensure the class balance of the outcome measures, the training cohort was oversampled, resulting in an increase of 77 cases in the minority class. After variables processing and feature selecting, optimal artificial intelligence-based model was constructed to predict the Ki67 expression level, and the model performance, interpretation and application development was performed. Results: The baseline characteristics of enrolled patients were described, and no statistically significant differences were found between two centers and cohorts, both before and after oversampling. The optimal model, regularized random forest, was constructed showing AUROC values of 0.802, 0.878, and 0.668, and balanced accuracy of 0.744, 0.808, and 0.679 in the oversampling training, validation, and test cohort, respectively. Model interpretation was performed, and a web application was built. Conclusions: An artificial intelligence-based predictive model for non-invasively assessing the Ki67 expression level of SRMs was developed, thus providing valuable reference for clinical decision-making in these patients.

Indexed as

artificial intelligenceCTKi67radiomicssmall renal mass

Identifiers

PMID40061892
PMCPMC11885116

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