Key result
Biodegradable polymer everolimus-eluting stents show a low 2.1% 1-year TLF rate in multivessel CAD.
Why the study?
Multivessel CAD poses challenges due to complexity and adverse outcomes, and real-world data on drug-eluting stents in Korean patients with multivessel disease are limited.
Observational (n=521)
Yes
Biodegradable polymer-coated everolimus-eluting stents demonstrated a low 1-year target lesion failure rate of 2.1% in real-world Korean patients with multivessel coronary artery disease.
Adds real-world evidence on these stents in multivessel disease; leaves open the role of identified predictors pending randomized trials.
BACKGROUND: Multivessel coronary artery disease (CAD) poses a significant challenge in interventional cardiology due to its complexity and association with adverse clinical outcomes. Real-world data on the clinical performance of drug-eluting stents in Korean patients with multivessel disease (MVD) are limited. This study aimed to evaluate the efficacy and safety of the biodegradable polymer-coated everolimus-eluting stents (SYNERGY™, Boston Scientific Corporation, Natick, MA, USA) in treating patients with MVD in real-world clinical setting. METHODS: This multicenter, prospective, observational registry involved 22 hospitals in the Republic of Korea. Eligible patients presented with ≥ 70% stenosis in at least two vessels and were amenable for receiving percutaneous coronary intervention (PCI). The primary endpoint was target lesion failure ([TLF], the composite of cardiac death; target vessel myocardial infarction [MI]; and target lesion revascularization [TLR]) at 1 year. RESULTS: Between August 2016 and September 2018, 542 patients were enrolled. The mean age of the patients was 66.2 ± 10.4 years, and most of them were male (73.7%). Diabetes mellitus (DM) was present in 40.8% of patients, while 68.2% had acute coronary syndrome (ACS). The 1-year TLF was in 2.1%, with incidences of cardiac death 0.9%, MI 0.3%, TLR 0.9%, and stent thrombosis 0.3%. Subgroup analysis revealed no significant differences in the primary endpoint between patients with or without ACS, and DM. In-stent restenosis (hazard ratio [HR], 11.20; 95% confidence interval [CI], 2.20-56.91) and total stent length (HR, 1.02; 95% CI, 1.01-1.03) were identified as independent predictors of TLF. CONCLUSION: The 1-year TLF rate observed in our cohort (2.1%) was comparable to or lower than rates previously reported in studies evaluating drug-eluting stents in patients undergoing multivessel PCI. These results suggest that the biodegradable polymer-coated everolimus-eluting stents provide favorable clinical outcomes for this patient population in real-world clinical practice.
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Kim et al. (2026) conducted an observational in Multivessel coronary artery disease (n=521). Biodegradable polymer-coated everolimus-eluting stent (SYNERGY) was evaluated on Target lesion failure (TLF) at 1 year. In patients with multivessel coronary artery disease, treatment with biodegradable polymer-coated everolimus-eluting stents resulted in a 1-year target lesion failure rate of 2.1%.
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