Key result
Higher beta-blocker doses linked to ~5% greater LVEF recovery per 25 mg in anthracycline cardiotoxicity.
Why the study?
Neurohormonal blocking drugs are recommended for anthracycline-induced left ventricular dysfunction, but evidence supporting their benefit is limited.
Does a higher beta-blocker dose improve LVEF recovery in patients with anthracycline-induced left ventricular dysfunction?
Observational (n=104)
No
Does a higher beta-blocker dose improve LVEF recovery in patients with anthracycline-induced left ventricular dysfunction?
Answers are grounded in this paper and cite their sources.
Higher doses of beta-blockers and earlier detection of LVEF decline are independently associated with improved LVEF recovery in patients with anthracycline-induced cardiomyopathy.
Background Neurohormonal blocking drugs, like beta-blockers, angiotensin-converting enzyme inhibitors (ACEIs), and angiotensin receptor blockers (ARBs), are recommended for treating anthracycline-induced left ventricular dysfunction (AILVD). However, there is limited evidence supporting their benefit. Therefore, this study evaluated associations of neurohormonal blockers and other clinical factors with recovery of left ventricular ejection fraction (LVEF) in patients with AILVD. Methods This retrospective chart review assessed patients treated with at least one dose of anthracycline, then had ≥10% LVEF reduction or post-anthracycline LVEF value <50%, and then had a follow-up LVEF measurement ≥90 days later. The primary endpoint was LVEF recovery (highest follow-up LVEF−lowest LVEF post-anthracycline). Variables from univariable tests with P < .1 were incorporated in a multiple linear regression model for independent factors significantly associated with LVEF recovery ( P < .05). Results Out of 104 patients, 83% were female, 86% self-reported white race, 53% had breast cancer, median (IQR) age was 52 (22) years, and LVEF recovery was 14% (16%). The final multivariable model included 2 significant variables: beta-blocker dose after anthracycline exposure (every 25 mg increase in beta-blocker dose was associated with 5.0% increase in LVEF recovery; P = .0005) and the time between the start of the anthracycline and the lowest LVEF post-anthracycline (every 5-year increase in time was associated with 1.8% decrease in LVEF recovery; P = .0379). Conclusions In patients with AILVD, a higher beta-blocker dose and earlier detection of LVEF reduction post-anthracycline were significantly and independently associated with improved LVEF recovery. These findings need to be validated in a larger, independent cohort.
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Shugg et al. (2025) conducted an observational in Anthracycline-Induced Left Ventricular Dysfunction (n=104). Beta-blocker dose after anthracycline exposure vs. Lower beta-blocker dose was evaluated on LVEF recovery (highest follow-up LVEF - lowest LVEF post-anthracycline) (5.0% increase per 25 mg increase in beta-blocker dose, p=0.0005). In patients with anthracycline-induced left ventricular dysfunction, every 25 mg increase in beta-blocker dose was associated with a 5.0% increase in LVEF recovery (p=0.0005).
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