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Abstract

Background: According to the current guideline, statins should be provided to prevent anthracycline cardiotoxicity in high-risk cancer patients. This study aims to investigate the role of atorvastatin in preventing anthracycline-induced cardiac dysfunction among low-risk breast cancer patients. Methods: In this randomized, double-blinded, placebo-controlled trial, newly diagnosed breast cancer patients with low risk of cancer therapy-related cardiac dysfunction (CTRCD) were assigned to receive atorvastatin 40 mg or placebo. Echocardiography was performed before, at 3 and 6 months after the anthracycline treatment to determine changes in LVEF as a primary outcome. The secondary outcome included changes in global longitudinal strain (GLS), LV volume, high-sensitivity troponin T levels, the incidence of CTRCD and side effects from atorvastatin. Results:

A total of 40 patients were enrolled. The post-anthracycline LVEF was significantly reduced compared with the baseline in both groups. The post-anthracycline LVEF reduction was lower in the atorvastatin group, however, not statistically significant (4% in the placebo group vs 2% in the atorvastatin group; p = 0.32). LV Volume, GLS, and troponin T levels did not change after anthracycline in both groups. The incidence of CTRCD was similar in both groups (3 (14%) in placebo, 3 (15%) in atorvastatin; p value 0.89) Conclusions: In low-risk breast cancer patients, atorvastatin does not show significant benefit in lessening the reduction of LVEF at 6 months post-anthracycline treatment. There were no differences observed in GLS changes, troponin levels, or the incidence of CTRCD between the atorvastatin and placebo groups.

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Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.

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