Risk Factors for Paclitaxel-Induced Peripheral Neuropathy in Patients With Breast Cancer Publisher Pubmed



Ghoreishi Z¹ ; Keshavarz S² ; Asghari Jafarabadi M³ ; Fathifar Z⁴ ; Goodman KA⁵ ; Esfahani A⁶
Source: BMC Cancer Published:2018

Abstract

Background: Paclitaxel induced peripheral neuropathy (PIPN) is a major debilitating side effect of paclitaxel in patients with breast cancer with no fully known mechanisms. The aim of the study was to find out the possible risk factors for PIPN. Methods: Eligible patients with node positive breast cancer undergoing chemotherapy with paclitaxel were assessed. They belonged to an initial randomized controlled trial in which the effectiveness of omega-3 fatty acids in preventing and reducing severity of PIPN was evaluated (protocol ID: NCT01049295). Reduced total neuropathy score (r-TNS) was used for measuring PIPN. All analyses were performed adjusting for intervention effect. The association between age, BMI, BSA, pathological grade, molecular biomarkers and PIPN was evaluated. Results: Fifty-seven patients with breast cancer were investigated. Age was significantly associated with risk of PIPN (RR:1.50, P value =.024). Body mass index and BSA had significant association with severity of PIPN (B:1.28, P =.025; and B: 3.88, P =.010 respectively). Also, BSA showed a significant association with the risk of PIPN (RR: 2.28, P =.035; B: 3.88, P =.035). Incidence and severity of PIPN were much more pronounced in progesterone receptor positive (PR+) patients (RR:1.88, P =.015 and B:1.54, P =.012). Multivariate analysis showed that age and the status of PR+ were independent risk factor for incidence and the status of PR+ was the only independent risk factor for severity of PIPN. Conclusion: Age, BSA and the status of PR+, should be considered as the risk factors for PIPN before commencement of chemotherapy with paclitaxel in patients with breast cancer. Older patients, those with greater BSA and PR+ patients may need closer follow up and more medical attention due to greater incidence and severity of PIPN. © 2018 The Author(s).