Key result
Prophylactic nebivolol shows no benefit over placebo for preserving LVEF in doxorubicin-treated breast cancer patients.
Why the study?
Anthracyclines are widely used to treat breast cancer but cause cardiotoxicity, prompting this study to evaluate prophylactic nebivolol for preventing anthracycline-induced cardiotoxicity.
Does prophylactic nebivolol prevent anthracycline-induced cardiotoxicity in breast cancer patients undergoing doxorubicin chemotherapy?
RCT (n=80)
Single-blind
Randomized
No
Does prophylactic nebivolol prevent anthracycline-induced cardiotoxicity in breast cancer patients undergoing doxorubicin chemotherapy?
Absolute Event Rate: 61.9% vs 61.8%
Prophylactic nebivolol did not show a statistically significant cardioprotective effect against anthracycline-induced cardiotoxicity in breast cancer patients at 6 months.
Nebivolol does not prevent doxorubicin-induced LVEF decline; does not support prophylactic use and challenges cardioprotection hypothesis.
Background: Anthracyclines are extensively used in the treatment of breast cancer. However, these therapeutic agents are responsible for chemotherapy-induced cardiotoxicity. Aim of this study was to assess the effect of use of prophylactic nebivolol for the prevention of anthracycline-induced cardiotoxicity in breast cancer patients.Methods: This was a prospective, randomized, single-blind, and placebo-controlled trial involving 80 participants with breast cancer, scheduled to undergo chemotherapy with doxorubicin. Patients were randomly divided into two groups: the nebivolol group (n=40) to receive nebivolol 5 mg daily and the placebo group (n=40) to receive placebo. All patients were evaluated with baseline Electrocardiogram (ECG) and echocardiography prior to treatment, and at the 6-month follow-up. Echocardiography included 2D echocardiography, colour doppler and tissue doppler imaging.Results: The study groups had comparable baseline echocardiographic variables. At the 6-month echocardiographic follow-up, there were no changes of statistical significance in any 2D echocardiographic variables in either group. However, there were minimal reductions of 0.4% in left ventricular ejection fraction in the nebivolol group (62.2±4.4% to 61.9±4.2%, p=0.75) and 1.6% in the placebo group (62.8±3.6% to 61.8±3.2%, p=0.18). Doppler examinations also did not reveal any statistically significant changes in variables such as peak A velocity, peak E velocity, E/A ratio, isovolumic relaxation time, and isovolemic contraction time in either group.Conclusions: Prophylactic use of nebivolol treatment may possess cardioprotective properties against anthracycline-induced cardiotoxicity in breast cancer patients although not statistically significant in this study.
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Rudrapogu et al. (2019) conducted an RCT in Breast cancer (n=80). Nebivolol vs. Placebo was evaluated on Left ventricular ejection fraction (LVEF) at 6 months. Prophylactic nebivolol 5 mg daily resulted in a non-significant 0.4% reduction in left ventricular ejection fraction compared to a 1.6% reduction with placebo in breast cancer patients receiving doxorubicin.
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