In patients with hemodynamically stabilized acute heart failure with reduced ejection fraction (HFrEF), a combination therapy of sacubitril-valsartan therapy led to greater reductions in NT-proBNP concentration compared to enalapril therapy, according to new trial results presented at the American Heart Association 2018 Scientific Sessions.
The Comparison of Sacubitril–Valsartan versus Enalapril on Effect on NT-proBNP in Patients Stabilized from an Acute Heart Failure Episode (PIONEER-HF) included 881 randomized patients with HFrEF who were hospitalized for hemodynamically stable acute decompensated HF. Patients were randomized to either enalapril (n=441; target dose 10 mg twice daily) or sacubitril-valsartan (n=440; target dose, 97 mg sacubitril with 103 mg valsartan twice daily). The primary study outcome was time-averaged proportional change in NT-proBNP concentration from baseline at 4 weeks and 8 weeks. Safety outcomes included rates of worsening renal function, symptomatic hypotension, angioedema and hyperkalemia.
According to the study results, presented at the meeting by co-author Eric J. Velazquez, MD, of the Yale University School of Medicine, the time-averaged reduction in NT-proBNP concentration was significantly greater in the patients assigned to sacubitril-valsartan vs. enalapril. According to the manuscript, published simultaneously with the presentation in the New England Journal of Medicine, the ration of the geometric mean of the week 4 and week 8 values compared to baseline was 0.53 in the sacubitril-valsartan group vs. 0.75 in the enalapril group (ratio of change with sacubitril–valsartan vs. enalapril, 0.71; 95% CI, 0.63 to 0.81; P<0.001). In addition, sacubitril-valsartan was safe and well-tolerated; the rates of worsening renal function, hyperkalemia, symptomatic hypotension, and angioedema did not differ between study groups.