Evidence map›Paper›PMID 40624807›Full record

ArticleCancer reports (Hoboken, N.J.)2025

Comparison of Random Survival Forest Based-Overall Survival With Deep Learning and Cox Proportional Hazard Models in HER-2-Positive HR-Negative Breast Cancer.

Wenqi Cai, Yan Qi, Linhui Zheng, Huachao Wu, Chunqian Yang, Runze Zhang, Chaoyan Wu, Haijun Yu

Abstract readComparative Study
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

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4 · The record

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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

8 authors.

Wenqi CaiDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.ORCID 0000-0001-8460-7333
Yan QiDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Linhui ZhengDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Huachao WuDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Chunqian YangDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Runze ZhangDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Chaoyan WuDepartment of Integrated Traditional Chinese Medicine and Western Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Haijun YuDepartment of Radiation and Medical Oncology, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.ORCID 0000-0002-5346-7830

Funding

National Natural Science Foundation of China 82073349Natural Science Foundation of Hubei Province 2018CFB561Natural Science Foundation of Hubei Province 2024AFB799Natural Science Foundation of Hubei Province 2024AFD426Zhongnan Hospital of Wuhan University Science, Technology and Innovation Seed Fund ZNPY2016043
6 · The paper itself

Abstract

backgroundTraditional CoxPH models are limited in handling real-world data complexities. While machine learning models like RSF and DeepSurv show promise, their application and comparative evaluation in the HER2-positive/HR-negative breast cancer subtype require further validation.

aimsThis study aims to build a survival prediction model for breast cancer patients based on different methods. The optimal model will provide more accurate survival predictions for clinical decision-making of HER2 positive and HR negative cancer patients. METHODS AND

resultsThis study analyzed 8,119 HER2-positive HR-negative breast cancer patients from the SEER database, randomly allocated to training/validation/test cohorts (7:1:2 ratio). Predictive models were developed using five feature sets and three algorithms (Cox PH, RSF, DeepSurv), with feature selection optimized via Concordance index (C-index). Evaluation revealed: The C-index of the DeepSurv models constructed using the training set is greater than 0.8, performing better than both the RSF and CoxPH models. However, CoxPH outperforms DeepSurv in terms of C-index when testset. The Brier scores for all models were below 0.25. Which indicates that the models predicted with high accuracy. Based on the training set, the Deepsurv model predicted the highest ROC-AUCs of 0.91, 0.863, and 0.855 for 1-, 3-, and 5-year overall survival (OS), respectively. The RSF model achieved the highest AUCs, specifically 0.876, 0.861, and 0.845, for 1-, 3-, and 5-year overall survival in the test group. The calibration graphs indicate that of the three models forecasting overall survival at 1, 3, and 5 years, the RSF model demonstrated the greatest level of agreement between predictions and actual observations, trailed by the DeepSurv model. There was poor agreement between CoxPH model predictions and observed data. Optimal Clinical Net Benefits at 1, 3, and 5 Years for DCA of the Deepsurv Model in the Training Set Data. However, in the test set, compared to other models, RSF showed better Optimal Clinical Net Benefits.

conclusionsIn conclusion, compared to conventional prognostic models, the Random Survival Forest (RSF) model serves as a reliable tool for predicting long-term survival in breast cancer patients, demonstrating consistent performance across diverse datasets. Furthermore, the feature set selected via RSF-Variable Importance (VIMP) (compared with LASSO regression and Cox regression) significantly enhances the performance of prognostic models. Our findings may offer practical guidance for future development of long-term prognostic models tailored to breast cancer subtypes.

Indexed as

Breast NeoplasmsDeep LearningErb-b2 Receptor Tyrosine KinasesAdultAgedFemaleHumansMiddle AgedPrognosisProportional Hazards ModelsReceptors, EstrogenReceptors, ProgesteroneSEER ProgramSurvival RateERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, Progesteronebreast cancerCoxPHDeepsurvRSFRSF‐VIMP

Identifiers

PMID40624807
PMCPMC12234386

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Registered trials

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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.