Key result
Sacubitril/valsartan improves LVEF by ~7% from baseline in anthracycline-induced cardiotoxicity.
Why the study?
The benefit of sacubitril/valsartan in ischemic heart failure is established, but whether it confers protective effects in anthracycline-induced cardiotoxicity remained unknown.
Does sacubitril/valsartan improve left ventricular ejection fraction and functional capacity in adult patients with anthracycline-induced cardiotoxicity?
Meta-Analysis (n=69)
Does sacubitril/valsartan improve left ventricular ejection fraction and functional capacity in adult patients with anthracycline-induced cardiotoxicity?
Mean Difference: 6.78 (95% CI 4.91–8.65)
p-value: p=<0.001
Sacubitril/valsartan may improve left ventricular ejection fraction, global longitudinal strain, and functional capacity in patients with anthracycline-induced cardiotoxicity.
Improves LVEF and GLS during chemotherapy but not CTRCD incidence; extends surrogate data while leaving clinical outcomes open for larger trials.
Background One of the adverse effects of anthracycline use is cardiotoxicity manifested as heart failure. The benefit of sacubitril/valsartan in patients with heart failure of ischemic origin has been demonstrated, but not due to toxicity. Our objective was to determine if there are protective effects of the use of sacubitril/valsartan in cardiotoxicity induced by anthracyclines. Methods A bibliographic search was carried out in PubMed, Cochrane Library, LILACS, Scopus, EBSCO and Google Scholar. A systematic review and meta-analysis was performed to assess mean differences (MD) with 95% confidence intervals following the PRISMA Statement. Results 558 published articles were found, of which three were submitted to analysis, with a total sample of 69 patients. With the use of sacubitril/valsartan there was an increase in the percentage of left ventricular ejection fraction (LVEF) [MD 6.78% (p < 0.001)], an increase in the percentage of global longitudinal strain of the left ventricle (LV-GLS) [MD 3.37 % (p < 0.001)], and decreased serum levels of NT-proBNP [MD −1003.64 pg/mL (p < 0.001)]; in addition, there was an increase in the distance traveled with the use of sacubitril/valsartan [MD 95.23 meters (p < 0.001)] compared to their baseline values, respectively. Conclusions This meta-analysis suggests that there is a benefit from the use of sacubitril/valsartan in patients with heart failure related to the use of anthracyclines on ventricular remodeling and functional capacity. This is the first meta-analysis to our knowledge evaluating this effect. Randomized double-blind placebo-controlled clinical trials are required to confirm these findings.
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Trejo et al. (2023) conducted a meta-analysis in Anthracycline-induced cardiotoxicity (n=69). Sacubitril/valsartan vs. Baseline values was evaluated on Percent change in Left Ventricular Ejection Fraction (LVEF) (MD 6.78%, 95% CI 4.91-8.65, p=<0.001). Sacubitril/valsartan significantly increased left ventricular ejection fraction by a mean difference of 6.78% compared to baseline in patients with anthracycline-induced cardiotoxicity.
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