European Heart Journal - Cardiovascular Pharmacotherapy · 2023 · 106 citations · 22 references
MedicineOncologyPharmacologyCancer PharmacologyCardio-oncologyChemotherapyAnthracycline CardiotoxicityCancer Therapy-related CardiotoxicityCardiac MedicationsCardiac PharmacotherapyCardiotoxicity ManagementCardiovascular DiseaseAcute Cardiac ToxicityAnthracycline-based ChemotherapyAnthracycline-induced CardiomyopathyAnthracycline-induced CardiotoxicityAnthracycline-induced Left Ventricular DysfunctionAnthracycline-related Heart FailureCardiotoxicityLeft Ventricular Ejection Fraction Decline
BACKGROUND AND AIMS: Anthracyclines can cause cancer therapy-related cardiac dysfunction (CTRCD). We aimed to assess whether statins prevent decline in left ventricular ejection fraction (LVEF) in anthracycline-treated patients at increased risk for CTRCD. METHODS: In this multicenter double-blinded, placebo-controlled trial, patients with cancer at increased risk of anthracycline-related CTRCD (per ASCO guidelines) were randomly assigned to atorvastatin 40 mg or placebo once-daily. Cardiovascular magnetic resonance (CMR) imaging was performed before and within 4 weeks after anthracyclines. Blood biomarkers were measured at every cycle. The primary outcome was post-anthracycline LVEF, adjusted for baseline. CTRCD was defined as a fall in LVEF by >10% to <53%. Secondary endpoints included left ventricular (LV) volumes, CTRCD, CMR tissue characterization, high sensitivity troponin I (hsTnI), and B-type natriuretic peptide (BNP). RESULTS: We randomized 112 patients (56.9 ± 13.6 years, 87 female, and 73 with breast cancer): 54 to atorvastatin and 58 to placebo. Post-anthracycline CMR was performed 22 (13-27) days from last anthracycline dose. Post-anthracycline LVEF did not differ between the atorvastatin and placebo groups (57.3 ± 5.8% and 55.9 ± 7.4%, respectively) when adjusted for baseline LVEF (P = 0.34). There were no significant between-group differences in post-anthracycline LV end-diastolic (P = 0.20) or end-systolic volume (P = 0.12), CMR myocardial edema and/or fibrosis (P = 0.06-0.47), or peak hsTnI (P ≥ 0.99) and BNP (P = 0.23). CTRCD incidence was similar (4% versus 4%, P ≥ 0.99). There was no difference in adverse events. CONCLUSIONS: In patients at increased risk of CTRCD, primary prevention with atorvastatin during anthracycline therapy did not ameliorate early LVEF decline, LV remodeling, CTRCD, change in serum cardiac biomarkers, or CMR myocardial tissue changes. TRIAL REGISTRATION: NCT03186404.
22
R: A Language and Environment for Statistical Computing
R Core Team · 2000 · 353K citations · Full text
Natural Sciences, Computer Science, Statistical Computing +10
Alexander R. Lyon, Teresa López‐Fernández, Liam S. Couch et al. · European Heart Journal · 2022 · 2.8K citations · Full text
Medicine, Hematology, Oncology +17
Early Detection of Anthracycline Cardiotoxicity and Improvement With Heart Failure Therapy
Daniela Cardinale, Alessandro Colombo, Giulia Bacchiani et al. · Circulation · 2015 · 1.7K citations
Medicine, Cardiology, Oncology +16
Edward H. Romond, Jong‐Hyeon Jeong, Priya Rastogi et al. · Journal of Clinical Oncology · 2012 · 519 citations · Full text
Medicine, Oncology, Pharmacology +17