Prophylactic Statin Therapy for the Prevention of Anthracycline-Induced Cardiotoxicity in Patients with Breast Cancer: A Systematic Review and Meta-Analysis of Randomized Controlled Trials and Cohort Studies

Authors

  • Nadia Karimah Amalia Trainee of Hematology and Medical Oncology Division, Internal Medicine Department, Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  • Yenny Dian Andayani Division of Hematology and Medical Oncology, Internal Medicine Department, Universitas Sriwijaya, Palembang, Indonesia
  • Mediarty Division of Hematology and Medical Oncology, Internal Medicine Department, Universitas Sriwijaya, Palembang, Indonesia
  • Norman Djamaludin Division of Hematology and Medical Oncology, Internal Medicine Department, Universitas Sriwijaya, Palembang, Indonesia

DOI:

https://doi.org/10.37275/bsm.v10i7.1634

Keywords:

anthracyclines, breast cancer, cardiotoxicity, cardio-oncology, meta-analysis, statins

Abstract

Background. Anthracycline-based chemotherapy remains a cornerstone of curative-intent breast-cancer treatment but carries a dose-dependent risk of cancer therapy-related cardiac dysfunction (CTRCD). Statins exert pleiotropic anti-inflammatory, antioxidative, and endothelial-stabilizing effects that may attenuate myocardial injury; however, prior meta-analyses pooled breast-cancer and lymphoma populations, obscuring breast-cancer-specific signals.

Methods. A systematic review and random-effects meta-analysis was conducted per PRISMA 2020. PubMed, Cochrane, Scopus, and Web of Science were searched for randomized controlled trials (RCTs) and propensity-matched cohort studies enrolling adult breast-cancer patients receiving anthracycline-based chemotherapy with or without trastuzumab. Co-primary outcomes were CTRCD incidence and standardized change in left-ventricular ejection fraction (LVEF, Hedges' g). Risk of bias was assessed using RoB 2.0 and ROBINS-I. Sensitivity analyses included leave-one-out exclusion and restriction to breast-cancer-only RCTs.

Results. Ten studies (1,239 patients; six RCTs, four cohort studies) were included. The pooled risk ratio for CTRCD was 0.49 (95% CI 0.28–0.85; p = 0.011; I² = 0%). The pooled standardized mean difference for LVEF change was 0.38 (95% CI −0.06 to 0.81; I² = 81%), corresponding to approximately +2.1 LVEF percentage points. Sensitivity analyses restricted to breast-cancer-only RCTs strengthened the CTRCD effect (RR 0.36, 95% CI 0.16–0.82). HER2-positive subgroup analyses yielded a pooled RR of 0.28 (95% CI 0.10–0.80).

Conclusion. Prophylactic statin therapy is associated with a clinically meaningful and statistically significant reduction in CTRCD in breast-cancer patients receiving anthracyclines. The protective effect is particularly pronounced in HER2-positive patients. A cautious, risk-stratified use of statins as a cardioprotective adjunct is supported pending adequately powered, breast-cancer-specific randomized trials.

Authors

  • Nadia Karimah Amalia1*
  • Yenny Dian Andayani2
  • Mediarty2
  • Norman Djamaludin2
  1. 1Trainee of Hematology and Medical Oncology Division, Internal Medicine Department, Faculty of Medicine, Universitas Sriwijaya, Palembang, Indonesia
  2. 2Division of Hematology and Medical Oncology, Internal Medicine Department, Universitas Sriwijaya, Palembang, Indonesia

Corresponding author Nadia Karimah Amalia — nadrimalia@gmail.com

Article history

  1. Submitted
  2. Accepted
  3. Published

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Published

2026-06-01

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How to Cite

1.
Amalia NK, Andayani YD, Mediarty, Djamaludin N. Prophylactic Statin Therapy for the Prevention of Anthracycline-Induced Cardiotoxicity in Patients with Breast Cancer: A Systematic Review and Meta-Analysis of Randomized Controlled Trials and Cohort Studies. Bioscmed [Internet]. 2026 Jun. 1 [cited 2026 Aug. 6];10(7):2561-78. Available from: https://bioscmed.com/index.php/bsm/article/view/1634

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