ArticleScientific reports2026
Pre-treatment vitamin D insufficiency predicts severe paclitaxel-induced sensory neuropathy in breast cancer patients: a prospective cohort study.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Paclitaxel-induced peripheral neuropathy (CIPN) is a debilitating side effect affecting up to 70% of patients receiving paclitaxel chemotherapy, with severe symptoms occurring in approximately 30%. While non-modifiable risk factors such as age and genetics have been established, the role of modifiable factors, including vitamin D insufficiency, remains poorly characterized. This study aimed to evaluate the association between pre-treatment vitamin D levels and the incidence of severe CIPN in breast cancer patients receiving paclitaxel-based chemotherapy. A prospective cohort study was conducted on 300 breast cancer patients (stage I-III) receiving paclitaxel-based chemotherapy (80 mg/m²) for 12 weeks at Kafrelsheikh University Hospitals. Baseline serum 25(OH)D was quantified using the Elecsys Vitamin D Total II assay on the Cobas e411 platform, standardized to the VDSP reference method. Pre-treatment vitamin D levels were measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS), with insufficiency defined as ≤ 20 ng/mL. CIPN was assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Chemotherapy-Induced Peripheral Neuropathy 20-item scale (EORTC QLQ-CIPN20), with particular focus on grade 3-4 sensory neuropathy. Statistical analyses included receiver operating characteristic (ROC) curves and multivariate logistic regression to identify independent risk factors. The mean pre-treatment vitamin D level was 23.45 ± 8.3 ng/mL, with 39.3% (118/300) of patients classified as having vitamin D insufficiency. Patients with vitamin D insufficiency demonstrated significantly higher rates of grade 3-4 sensory CIPN compared to those with sufficient levels (32.2% vs. 5.5%, p < 0.001). Mean vitamin D levels were significantly lower in patients who developed severe CIPN (17.5 ± 4.9 ng/mL vs. 24.6 ± 8.4 ng/mL, p < 0.001). ROC analysis demonstrated vitamin D's predictive value for motor CIPN (AUC = 0.747, p = 0.038). Multivariate logistic regression analysis confirmed vitamin D insufficiency as an independent predictor of sensory CIPN (OR = 6.72, 95% CI: 3.09-14.61, p < 0.001), even after adjusting for age, body mass index, and treatment schedule. Vitamin D insufficiency is independently associated with an increased risk of severe paclitaxel-induced peripheral neuropathy in breast cancer patients. While causal inference cannot be drawn from this observational design, these findings provide a strong rationale for future randomized controlled trials to evaluate whether vitamin D supplementation could serve as a candidate preventive strategy to mitigate CIPN severity and optimize cancer therapy outcomes.
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