Evidence map›Paper›PMID 41152747›Full record

SynthesisBMC medical research methodology2025

Comparison of machine learning methods versus traditional Cox regression for survival prediction in cancer using real-world data: a systematic literature review and meta-analysis.

Yinan Huang, Shadi Bazzazzadehgan, Jieni Li, Arman Arabshomali, Mai Li, Kaustuv Bhattacharya, John P Bentley

Abstract readSystematic ReviewMeta-AnalysisComparative Study
In one paragraph

Synthesis in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Exploration of the Prediction of the Survival Cycle and Influencing Factors of Chinese Patients With Advanced Cancer Based on Multi-Model Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

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

7 authors.

Yinan HuangDepartment of Pharmacy Administration, University of Mississippi School of Pharmacy, University, MS, USA. yhuang9@olemiss.edu.
Shadi BazzazzadehganDepartment of Pharmacy Administration, University of Mississippi School of Pharmacy, University, MS, USA.
Jieni LiDepartment of Pharmaceutical Health Outcomes and Policy, University of Houston College of Pharmacy, Houston, TX, USA.
Arman ArabshomaliDepartment of Pharmacy Administration, University of Mississippi School of Pharmacy, University, MS, USA.
Mai LiDepartment of Industrial Engineering, University of Houston Cullen College of Engineering, Houston, TX, USA.
Kaustuv BhattacharyaDepartment of Pharmacy Administration, University of Mississippi School of Pharmacy, University, MS, USA.
John P BentleyDepartment of Pharmacy Administration, University of Mississippi School of Pharmacy, University, MS, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate prediction of survival in oncology can guide targeted interventions. The traditional regression-based Cox proportional hazards (CPH) model has statistical assumptions and may have limited predictive accuracy. With the capability to model large datasets, machine learning (ML) holds the potential to improve the prediction of time-to-event outcomes, such as cancer survival outcomes. The present study aimed to systematically summarize the use of ML models for cancer survival outcomes in observational studies and to compare the performance of ML models with CPH models.

methodsWe systematically searched PubMed, MEDLINE (via EBSCO), and Embase for studies that evaluated ML models vs. CPH models for cancer survival outcomes. The use of ML algorithms was summarized, and either the area under the curve (AUC) or the concordance index (C-index) for the ML and CPH models were presented descriptively. Only studies that provided a measure of discrimination, i.e., AUC or C-index, and 95% confidence interval (CI) were included in the final meta-analysis. A random-effects model was used to compare the predictive performance in the pooled AUC or C-index estimates between ML and CPH models using R. The quality of the studies was evaluated using available checklists. Multiple sensitivity analyses were performed.

resultsA total of 21 studies were included for systematic review and 7 for meta-analysis. Across the 21 articles, diverse ML models were used, including random survival forest (N=16, 76.19%), gradient boosting (N=5, 23.81%), and deep learning (N=8, 38.09%). In predicting cancer survival outcomes, ML models showed no superior performance over CPH regression. The standardized mean difference in AUC or C-index was 0.01 (95% CI: -0.01 to 0.03). Results from the sensitivity analyses confirmed the robustness of the main findings.

conclusionsML models had similar performance compared with CPH models in predicting cancer survival outcomes. Although this systematic review highlights the promising use of ML to improve the quality of care in oncology, findings from this review also suggest opportunities to improve ML reporting transparency. Future systematic reviews should focus on the comparative performance between specific ML models and CPH regression in time-to-event outcomes in specific type of cancer or other disease areas.

Indexed as

Machine LearningNeoplasmsAlgorithmsArea Under CurveHumansPrognosisProportional Hazards ModelsSurvival AnalysisCancerCox proportional hazards modelMachine learningReal-world dataSurvival analysis

Identifiers

PMID41152747
PMCPMC12570641

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.