ArticleCancers2026
Revisiting AI Interpretability in Precision Oncology: Why Predictive Accuracy Does Not Ensure Stable Feature Importance.
Article in Cancers, 2026. 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
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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.
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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.
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Who cites it
3 citing papers in PubMed.
- Feature Importance Bias and Competing Risks: Methodological Concerns in Ensemble Models for Diabetic Kidney Disease.Diabetes, obesity & metabolism · 2026Article
- Editorial: Revolutionizing nutritional epidemiology: harnessing digital health, AI, and big data for population-level disease prevention and management.Frontiers in nutrition · 2026Article
- Application of the artificial intelligence-assisted World Café teaching model in clinical pharmacology graduate course: a pilot study.Frontiers in public health · 2026Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundArtificial intelligence (AI) is becoming important in oncology, supporting risk prediction, treatment planning, and biomarker discovery. However, current evaluation practices often assume that high predictive accuracy implies reliable interpretation-a misconception that may undermine reproducibility and clinical decision-making. This study aims to reassess interpretability by introducing feature ranking order consistency as a stability-focused metric to evaluate how model explanations respond to minimal input perturbations.
methodsUsing The Cancer Genome Atlas (TCGA) breast cancer multi-omics dataset, we compared supervised models-Linear Regression, Least Absolute Shrinkage and Selection Operator (LASSO), Random Forest, and Extreme Gradient Boosting (XGBoost)-with unsupervised and statistical methods, including Principal Component Analysis (PCA), Highly Variable Gene Selection, and Spearman's rank correlation. Each method produced a Top 20 feature ranking, and stability was assessed by testing whether rankings remained consistent after removing the top-ranked feature. Predictive performance was evaluated using a Random Forest classifier with stratified 10-fold cross-validation.
resultsSupervised models exhibited unstable feature importance rankings even under minimal perturbations (<0.1% feature removal), suggesting that high predictive accuracy may obscure fragile or misleading explanations. In contrast, Highly Variable Gene Selection and Spearman's correlation consistently produced stable, biologically coherent feature sets and maintained competitive predictive performance.
conclusionsInterpretive instability is a major limitation of many machine learning models in oncology. Incorporating stability-based criteria-such as feature ranking consistency-into evaluation frameworks is essential for ensuring reproducible, trustworthy, and clinically actionable AI. As AI adoption accelerates, prioritizing interpretability alongside accuracy is critical for responsible deployment in precision oncology.
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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.