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Risk Prediction Model for Taxane-Induced Peripheral Neuropathy in Early-Stage Cancer
Meghna S Trivedi1, Joseph M Unger2,3, N Lynn Henry4
1Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York.
JAMA Network Open
|April 10, 2026
Summary
A new risk prediction model identifies patients at high risk for taxane-induced peripheral neuropathy (TIPN). This model aids in personalized cancer treatment decisions and monitoring for chemotherapy side effects.
Area of Science:
- Oncology
- Neurology
- Clinical Trials
Background:
- Taxane-induced peripheral neuropathy (TIPN) significantly impacts cancer patients' quality of life and treatment adherence.
- Effective interventions for preventing and treating TIPN remain limited.
Purpose of the Study:
- To develop and validate a predictive model for identifying patients at risk of developing TIPN.
Main Methods:
- A prospective observational cohort study (SWOG S1714) involving 1278 participants receiving taxane-based chemotherapy.
- A risk prediction model was developed using logistic regression and cross-validation on a training set (n=768) and validated on a test set (n=510).
- TIPN occurrence was assessed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Chemotherapy-Induced Peripheral Neuropathy 20-item scale (CIPN-20) by week 24.
Main Results:
- Over 60% (804 of 1278) of participants experienced TIPN by week 24.
- The validated risk model included factors such as paclitaxel use, advanced disease stage, treatment duration, comorbidities (diabetes, autoimmune disease, kidney disease, neurologic conditions), and patient race/ethnicity.
- The model successfully stratified risk, with high-risk patients experiencing TIPN at a significantly higher rate (68.1%) compared to low-risk patients (50.9%) in the test set.
Conclusions:
- A validated risk prediction model incorporating baseline factors can effectively stratify TIPN risk in cancer patients.
- This model can potentially guide clinical decision-making, enhance symptom monitoring, and inform enrollment in targeted interventional trials for TIPN prevention and management.
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