Carvedilol for Prevention of Chemotherapy-Related Cardiotoxicity: The CECCY Trial
- PMID: 29540327
- DOI: 10.1016/j.jacc.2018.02.049
Carvedilol for Prevention of Chemotherapy-Related Cardiotoxicity: The CECCY Trial
Abstract
Background: Anthracycline (ANT) chemotherapy is associated with cardiotoxicity. Prevention with β-blockers remains controversial.
Objectives: This prospective, randomized, double-blind, placebo-controlled study sought to evaluate the role of carvedilol in preventing ANT cardiotoxicity.
Methods: The authors randomized 200 patients with HER2-negative breast cancer tumor status and normal left ventricular ejection fraction (LVEF) referred for ANT (240 mg/m2) to receive carvedilol or placebo until chemotherapy completion. The primary endpoint was prevention of a ≥10% reduction in LVEF at 6 months. Secondary outcomes were effects of carvedilol on troponin I, B-type natriuretic peptide, and diastolic dysfunction.
Results: Primary endpoint occurred in 14 patients (14.5%) in the carvedilol group and 13 patients (13.5%) in the placebo group (p = 1.0). No differences in changes of LVEF or B-type natriuretic peptide were noted between groups. A significant difference existed between groups in troponin I levels over time, with lower levels in the carvedilol group (p = 0.003). Additionally, a lower incidence of diastolic dysfunction was noted in the carvedilol group (p = 0.039). A nonsignificant trend toward a less-pronounced increase in LV end-diastolic diameter during the follow-up was noted in the carvedilol group (44.1 ± 3.64 mm to 45.2 ± 3.2 mm vs. 44.9 ± 3.6 mm to 46.4 ± 4.0 mm; p = 0.057).
Conclusions: In this largest clinical trial of β-blockers for prevention of cardiotoxicity under contemporary ANT dosage, the authors noted a 13.5% to 14.5% incidence of cardiotoxicity. In this scenario, carvedilol had no impact on the incidence of early onset of LVEF reduction. However, the use of carvedilol resulted in a significant reduction in troponin levels and diastolic dysfunction. (Carvedilol Effect in Preventing Chemotherapy-Induced Cardiotoxicity [CECCY]; NCT01724450).
Keywords: cardiomyopathy; chemotherapy; prevention; troponin; β-blockers.
Copyright © 2018 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Comment in
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Beta-Blockers for Primary Prevention of Anthracycline Cardiotoxicity: Not Quite Ready for Prime Time.J Am Coll Cardiol. 2018 May 22;71(20):2291-2292. doi: 10.1016/j.jacc.2018.03.461. J Am Coll Cardiol. 2018. PMID: 29773156 No abstract available.
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Can Carvedilol Prevent Chemotherapy-Related Cardiotoxicity?: A Dream to Be Balanced With Tolerability.J Am Coll Cardiol. 2018 Sep 4;72(10):1181-1182. doi: 10.1016/j.jacc.2018.05.071. J Am Coll Cardiol. 2018. PMID: 30165996 No abstract available.
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Reply: Can Carvedilol Prevent Chemotherapy-Related Cardiotoxicity?: A Dream to Be Balanced With Tolerability.J Am Coll Cardiol. 2018 Sep 4;72(10):1182-1183. doi: 10.1016/j.jacc.2018.07.003. J Am Coll Cardiol. 2018. PMID: 30165997 No abstract available.
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