Key result
Finerenone cuts major cardiovascular events ~22% vs. placebo in stage 4 CKD and T2D.
Why the study?
Patients with stage 4 CKD and type 2 diabetes have limited treatment options to reduce their persistent cardiovascular and kidney risk.
Does finerenone reduce cardiovascular and kidney events in participants with stage 4 CKD and type 2 diabetes?
RCT (n=890)
Double-blind
1:1
Yes
Does finerenone reduce cardiovascular and kidney events in participants with stage 4 CKD and type 2 diabetes?
Hazard Ratio: 0.78 (95% CI 0.57–1.07)
Absolute Event Rate: 17% vs 20%
In patients with stage 4 CKD and type 2 diabetes, finerenone demonstrated cardiovascular benefits and a safety profile consistent with earlier stages of CKD, though the kidney composite outcome effect was inconsistent over time.
May support finerenone for CV protection in stage 4 CKD with T2D; extends prior evidence to advanced kidney disease.
BACKGROUND: Patients with stage 4 CKD and type 2 diabetes have limited treatment options to reduce their persistent cardiovascular and kidney risk. In Finerenone in Chronic Kidney Disease and Type 2 Diabetes (FIDELITY), a prespecified pooled analysis of Finerenone in Reducing Kidney Failure and Disease Progression in Diabetic Kidney Disease (FIDELIO-DKD) and Finerenone in Reducing Cardiovascular Mortality and Morbidity in Diabetic Kidney Disease (FIGARO-DKD), finerenone improved heart-kidney outcomes in participants with CKD and type 2 diabetes. METHODS: This FIDELITY subgroup analysis investigated the effects of finerenone in participants with stage 4 CKD (eGFR <30 ml/min per 1.73 m 2 ). Efficacy outcomes included a cardiovascular composite (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure) and a kidney composite (kidney failure, sustained ≥57% decrease in eGFR from baseline, or kidney disease death). RESULTS: Of 13,023 participants, 890 (7%) had stage 4 CKD. The hazard ratio for risk of cardiovascular composite outcome with finerenone versus placebo was 0.78 (95% confidence interval, 0.57 to 1.07). The kidney composite outcome proportional hazards assumption was not met for the overall study period, with a protective effect only shown up to 2 years, after which the direction of association was inconsistent, and an observed loss of precision over time incurred on finerenone versus placebo risk differences. Nonetheless, albuminuria and rate of eGFR decline were consistently reduced with finerenone versus placebo. Adverse events were balanced between treatment arms. Hyperkalemia was the most common adverse event reported (stage 4 CKD: 26% and 13% for finerenone versus placebo, respectively); however, the incidence of hyperkalemia leading to permanent discontinuation was low (stage 4 CKD: 3% and 2% for finerenone versus placebo, respectively). CONCLUSIONS: The cardiovascular benefits and safety profile of finerenone in participants with stage 4 CKD were consistent with the overall FIDELITY population; this was also the case for albuminuria and the rate of eGFR decline. The effects on the composite kidney outcome were not consistent over time.
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Sarafidis et al. (2023) conducted an RCT in Stage 4 CKD and Type 2 Diabetes (n=890). Finerenone vs. Placebo was evaluated on Cardiovascular composite (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure) (HR 0.78, 95% CI 0.57 to 1.07). Finerenone reduced the risk of the cardiovascular composite outcome (HR 0.78) compared to placebo in patients with stage 4 CKD and type 2 diabetes, alongside consistent reductions in albuminuria.
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