Cardiac effects of granisetron in a prospective crossover randomized dose comparison trial

Purpose

Cardiac side effects of granisetron have been studied mostly in adult patients that are using cardiotoxic chemotherapeutics. There is limited evidence in pediatric age group and no information in pediatric oncology patients with non-cardiotoxic chemotherapeutics.

Methods

In this prospective, crossover randomized study, the cardiac side effects of granisetron are compared in pediatric oncology patients who had carboplatin based chemotherapy. They were randomized to receive either 10 or 40 μg kg^?1 dose^?1 of granisetron before each cycle of chemotherapy. We drew blood for creatine phosphokinase (CPK), CPK-muscle band (MB) and Troponin-T before and 24?h after administering granisetron. Electrocardiography (ECG) tracings were taken at 0, 1, 2, 3, 6 and 24?h of granisetron. Twenty-four hours Holter ECG monitorisation was performed after each granisetron infusion.

Results

A total of 16 patients (median 8.7?years of age) were treated with weekly consecutive courses of carboplatin. There was bradycardia (p?=?0.000) in patients that had granisetron at 40 μg/kg and PR interval was shortened in patients that had granisetron at 10 μg/kg dose (p?=?0.021). At both doses of granisetron, QTc interval and dispersion were found to be similar. CPK, CK-MB and Troponin-T values were found to be normal before and 24?h after granisetron infusion.

Conclusions

As the first study that has studied cardiac side effects of granisetron in patients that are not using cardiotoxic chemotherapeutics, we conclude that granisetron at 40 μg kg^?1 dose^?1 causes bradycardia only. We have also demonstrated that granisetron does not cause any clinically cardiac side effects either at 10 or 40 μg kg^?1 dose^?1. However, our results should be supported by prospective randomized studies with larger samples of patient groups.