Statins as preventive therapy for anthracycline cardiotoxicity: a meta-analysis of randomized controlled trials

Int J Cardiol. 2023 Nov 15:391:131219. doi: 10.1016/j.ijcard.2023.131219. Epub 2023 Jul 30.

Abstract

Background: Cardiotoxicity occurs in 5-20% of cancer patients who receive anthracyclines. The aim of this study was to pool all the randomized controlled trials (RCTs) investigating the cardio-protective role of statins in patients treated with anthracyclines.

Methods: PubMed and Scopus electronic databases were scanned for eligible studies up to May 3rd, 2023. A total of 5 RCTs with 808 patients were included. Efficacy endpoints were the rate of anthracycline-mediated cardiotoxicity, the incidence of hospitalization for heart failure (HF), left ventricular ejection fraction (LVEF) value after anthracycline treatment, and ∆LVEF calculated as the difference in LVEF before and after anthracycline therapy. Safety endpoints [i.e., the incidence of muscle pain and serious adverse events (SAE)] were also assessed.

Results: On pooled analysis, the statin-treated group had a lower incidence of cardiotoxicity compared to the placebo group [risk ratio (RR) 0.52, 95% confidence Interval (CI) 0.33-0.83, P = 0.01; I2 = 0%], as well as higher mean LVEF [Mean difference (MD) 1.88, 95% CI 0.66-3.1, P < 0.01; I2 = 57.3%)] and a more favorable ∆LVEF during follow-up (MD 2.38, 95% CI -0.03 - +4.79, P = 0.05; I2 = 99%), despite no significant difference in terms of hospitalization for HF and rate of adverse events. Of note, severe heterogeneity affected the analyses for both LVEF and ΔLVEF.

Conclusions: The current meta-analysis of all RCTs conducted so far shows an overall beneficial effect of statins on the risk of anthracyclines-induced cardiotoxicity and LVEF preservation. No difference was observed in the rate of HF hospitalization. More powered RCTs are needed to fully investigate the impact of statins on prognosis in patients receiving anthracyclines therapy.

Keywords: Anthracyclines; Cardio-oncology; Cardiotoxicity; Statin.

Publication types

  • Meta-Analysis

MeSH terms

  • Anthracyclines / adverse effects
  • Antibiotics, Antineoplastic / adverse effects
  • Cardiotoxicity / etiology
  • Cardiotoxicity / prevention & control
  • Heart Failure* / chemically induced
  • Heart Failure* / drug therapy
  • Heart Failure* / prevention & control
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / pharmacology
  • Randomized Controlled Trials as Topic
  • Stroke Volume

Substances

  • Anthracyclines
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Antibiotics, Antineoplastic