ArticleFrontiers in oncology2025
Combining clinical characteristics with CT radiomics to predict Ki67 expression level of small renal mass based on artificial intelligence algorithms.
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.
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
3 citing papers in PubMed.
- Development and validation of a deep learning radiomics model for predicting capsular invasion in small renal masses: a multicenter retrospective study.Quantitative imaging in medicine and surgery · 2026Article
- Integration of multi-scale radiomics and deep learning for Ki-67 prediction in clear cell renal carcinoma.NPJ precision oncology · 2025Article
- Development and validation of a fusion model based on multi-phase contrast CT radiomics combined with clinical features for predicting Ki-67 expression in gastric cancer.Biomedical reports · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
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.