Effect of cilostazol on preventing paclitaxel‐induced neuropathy in patients with breast cancer: A randomized controlled trial

Author:

Haroun Esraa A.1ORCID,Mansour Noha O.1ORCID,Eltantawy Ahmed2ORCID,Shams Mohamed E. E.1ORCID

Affiliation:

1. Clinical Pharmacy and Pharmacy Practice Department, Faculty of Pharmacy Mansoura University Mansoura Egypt

2. Medical Oncology Unit, Oncology Center Mansoura University Mansoura Egypt

Abstract

AbstractStudy ObjectivePaclitaxel‐induced peripheral neuropathy is a significant clinical problem can markedly deteriorate patient's quality of life (QoL). Preclinical evidence exists about the preventive capacity of cilostazol against peripheral neuropathy. However, this hypothesis has not yet been clinically investigated. This proof‐of‐concept study evaluated the effect of cilostazol on the incidence of paclitaxel‐induced peripheral neuropathy in patients with non‐metastatic breast cancer.DesignThis is a parallel randomized placebo‐controlled trial.SettingThe Oncology Center at Mansoura University, Egypt.PatientsPatients with breast cancer scheduled to receive paclitaxel 175 mg/m2 biweekly.InterventionsPatients were randomized to either cilostazol group who received cilostazol tablets 100 mg BID, or to control group who received placebo instead.MeasurementsThe primary endpoint was the incidence of paclitaxel‐induced neuropathy evaluated through common terminology criteria for adverse event (NCI‐CTCAE) version 4. Secondary endpoints included assessment of the patient's QoL by the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group‐Neurotoxicity (FACT‐GOG‐NTx) subscale. Exploratory outcome measures included changes in serum levels of biomarkers namely nerve growth factor (NGF), and neurofilament light chain (NfL).Main ResultsThe incidence of grade 2 and 3 peripheral neuropathies were significantly lower in the cilostazol group (40%) compared to the control group (86.7%) (p < 0.001). The incidence of clinically significant worsening in neuropathy‐related QoL was higher in control group compared to the cilostazol group (p = 0.001). A higher percent increase from baseline in serum NGF was observed in the cilostazol group (p = 0.043). The circulating levels of NfL deemed comparable between the two arms at the end of the study (p = 0.593).ConclusionAdjunctive use of cilostazol is as a novel option that might reduce the incidence of paclitaxel‐induced peripheral neuropathy and improve the patients' QoL. Future larger clinical trials are warranted to confirm these findings.

Publisher

Wiley

Subject

Pharmacology (medical)

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