Key result
Three years after stenting all-comers with bifurcation lesions, target vessel failure was similar with sirolimus-eluting (HR 0.84) and everolimus-eluting stents (HR 0.79) versus zotarolimus-eluting stents.
Why the study?
Coronary bifurcation lesions are frequently treated in routine practice, but data regarding the performance of very thin-strut biodegradable polymer drug-eluting stents in this setting are scarce.
Do very thin-strut biodegradable polymer-coated sirolimus- or everolimus-eluting stents improve target vessel failure compared to thin-strut durable polymer-coated zotarolimus-eluting stents in all-comer patients with coronary bifurcation lesions?
RCT (n=1,236)
Patient- and assessor-blinded
Equally randomized
Yes
Do very thin-strut biodegradable polymer-coated sirolimus- or everolimus-eluting stents improve target vessel failure compared to thin-strut durable polymer-coated zotarolimus-eluting stents in all-comer patients with coronary bifurcation lesions?
Hazard Ratio: 0.84 (95% CI 0.56–1.27)
Absolute Event Rate: 10.3% vs 12.1%
p-value: p=0.40
In patients with coronary bifurcation lesions, very thin-strut biodegradable polymer-coated sirolimus- and everolimus-eluting stents showed similar 3-year clinical outcomes compared to thin-strut durable polymer-coated zotarolimus-eluting stents.
Supports use of very thin-strut BP-DES for bifurcation lesions; extends all-comers RCT data to this complex subgroup.
BACKGROUND: Treatment of a coronary bifurcation lesion is often required in routine clinical practice, but data on the performance of very thin-strut biodegradable polymer drug-eluting stents are scarce. METHODS: Comparison of biodegradable polymer and durable polymer drug-eluting stents in an all comers population (BIO-RESORT) is a prospective, multicenter randomized clinical trial that included 3514 all-comer patients, who were randomized to very thin-strut biodegradable polymer-coated sirolimus- or everolimus-eluting stents, versus thin-strut durable polymer-coated zotarolimus-eluting stents. The approach of bifurcation stenting was left at the operator's discretion, and provisional stenting was generally preferred. This prespecified analysis assessed 3-year clinical outcome of all patients in whom treatment involved at least one bifurcation with a side-branch diameter ≥1.5 mm. RESULTS: Of all BIO-RESORT trial participants, 1236 patients were treated in bifurcation lesions and analyzed. Single- and two-stent techniques were used in 85.8% and 14.2%, respectively. 'True' bifurcation lesions (main vessel and side-branch obstructed) were treated in 31.1%. Three-year follow-up was available in 1200/1236 (97.1%) patients. The main endpoint target vessel failure (composite of cardiac death, target vessel-related myocardial infarction, or target vessel revascularization) occurred in sirolimus-eluting stents in 42/412 (10.3%) and in zotarolimus-eluting stents in 49/409 (12.1%) patients (P-logrank = 0.40). In everolimus-eluting stents, target vessel failure occurred in 40/415 (9.8%) patients (vs. zotarolimus-eluting stents: P-logrank = 0.26). There was no between-stent difference in individual components of target vessel failure. Findings were consistent in patients with single-vessel treatment and patients treated with a single-stent technique. CONCLUSIONS: Three years after stenting all-comers with bifurcation lesions, clinical outcome was similar with the sirolimus-eluting and everolimus-eluting stents versus the zotarolimus-eluting stent.
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Buiten et al. (2020) conducted an RCT in Coronary bifurcation lesions (n=1,236). Sirolimus-eluting or everolimus-eluting stents vs. Zotarolimus-eluting stents was evaluated on Target vessel failure (composite of cardiac death, target vessel-related myocardial infarction, or target vessel revascularization) (HR 0.84, 95% CI 0.56-1.27, p=0.40). Three years after stenting all-comers with bifurcation lesions, target vessel failure was similar with sirolimus-eluting (HR 0.84) and everolimus-eluting stents (HR 0.79) versus zotarolimus-eluting stents.
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