Evidence map›Paper›PMID 41749845›Full record

ArticleCancers2026

Revisiting AI Interpretability in Precision Oncology: Why Predictive Accuracy Does Not Ensure Stable Feature Importance.

Souichi Oka, Yoshiyasu Takefuji

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

2 authors.

Souichi OkaScience Park Corporation, 3-24-9 Iriya-Nishi, Zama 252-0029, Japan.ORCID 0009-0000-4840-5232
Yoshiyasu TakefujiFaculty of Data Science, Musashino University, 3-3-3 Ariake, Koto-ku, Tokyo 135-8181, Japan.ORCID 0000-0002-1826-742X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

artificial intelligenceexplainable AIfeature importancefeature ranking consistencyinterpretabilitymulti-omicspredictive accuracy

Identifiers

PMID41749845
PMCPMC12939461

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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.