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Updated: Jun 7, 2025

An R-Based Landscape Validation of a Competing Risk Model
Published on: September 16, 2022
Balancing accuracy and Interpretability: An R package assessing complex relationships beyond the Cox model and
Diana Shamsutdinova1, Daniel Stamate2, Daniel Stahl1
1Department of Biostatistics and Health Informatics, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
Background:
Accurate and interpretable models are essential for clinical decision-making, where predictions can directly impact patient care. Machine learning (ML) survival methods can handle complex multidimensional data and achieve high accuracy but require post-hoc explanations. Traditional models such as the Cox Proportional Hazards Model (Cox-PH) are less flexible, but fast, stable, and intrinsically transparent. Moreover, ML does not always outperform Cox-PH in clinical settings, warranting a diligent model validation. We aimed to develop a set of R functions to help explore the limits of Cox-PH compared to the tree-based and deep learning survival models for clinical prediction modelling, employing ensemble learning and nested cross-validation.
Methods:
We developed a set of R functions, publicly available as the package "survcompare". It supports Cox-PH and Cox-Lasso, and Survival Random Forest (SRF) and DeepHit are the ML alternatives, along with the ensemble methods integrating Cox-PH with SRF or DeepHit designed to isolate the marginal value of ML. The package performs a repeated nested cross-validation and tests for statistical significance of the ML's superiority using the survival-specific performance metrics, the concordance index, time-dependent AUC-ROC and calibration slope. To get practical insights, we applied this methodology to clinical and simulated datasets with varying complexities and sizes.
Results:
In simulated data with non-linearities or interactions, ML models outperformed Cox-PH at sample sizes ≥ 500. ML superiority was also observed in imaging and high-dimensional clinical data. However, for tabular clinical data, the performance gains of ML were minimal; in some cases, regularised Cox-Lasso recovered much of the ML's performance advantage with significantly faster computations. Ensemble methods combining Cox-PH and ML predictions were instrumental in quantifying Cox-PH's limits and improving ML calibration. Traditional models like Cox-PH or Cox-Lasso should not be overlooked while developing clinical predictive models from tabular data or data of limited size.
Conclusion:
Our package offers researchers a framework and practical tool for evaluating the accuracy-interpretability trade-off, helping make informed decisions about model selection.
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