Finerenone attenuated the association between an initial eGFR decline ≥15% and worse clinical outcomes seen with placebo (P=0.50 for percent change in eGFR), supporting its continued use.
RCT
Double-blind
Parallel-Group
Yes
Does finerenone improve outcomes compared to placebo in patients with HFmrEF/HFpEF who experience an initial decline in eGFR?
An early decline in eGFR is anticipated with finerenone in HFmrEF/HFpEF and should not automatically lead to discontinuation of therapy.
BACKGROUND: An initial decline in estimated glomerular filtration rate (eGFR) often leads to reluctance to continue life-saving therapies in patients with heart failure (HF). OBJECTIVES: The goal of this study was to describe the association between initial decline in eGFR and subsequent clinical outcomes in patients randomized to placebo or finerenone. METHODS: In this prespecified analysis of FINEARTS-HF (Finerenone Trial to Investigate Efficacy and Safety Superior to Placebo in Patients with Heart Failure), we examined the association between initial decline in eGFR (≥15%) from randomization to 1 month and subsequent outcomes in patients assigned to finerenone or placebo. The primary outcome was the composite of total HF events and cardiovascular death. RESULTS: = 0.50 for percent change in eGFR), and safety, including hyperkalemia, was similar regardless of an early eGFR decline. CONCLUSIONS: Although an initial decline in eGFR was associated with worse outcomes in patients assigned to placebo, this relationship was not as strong in those treated with finerenone. An early decline in eGFR can be anticipated with finerenone and should not automatically lead to the discontinuation of this disease-modifying therapy (FINEARTS-HF Finerenone Trial to Investigate Efficacy and Safety Superior to Placebo in Patients with Heart Failure NCT04435626; A Multicenter, Randomized, Double-Bline, Parallel-Group, Placebo-Controlled Study to Evaluate the efficacy and safety of finerenone on morbidity and mortality in participants With Heart Failure NYHA II-IV and left ventricular ejection fraction ≥40% EudraCT 2020-000306-29).
Matsumoto et al. (Wed,) conducted a rct in Heart failure (NYHA II-IV) with left ventricular ejection fraction ≥40%. Finerenone vs. Placebo was evaluated on Composite of total HF events and cardiovascular death. Finerenone attenuated the association between an initial eGFR decline ≥15% and worse clinical outcomes seen with placebo (P=0.50 for percent change in eGFR), supporting its continued use.
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