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Six Versus 12 Months of Dual Antiplatelet Therapy After Implantation of Biodegradable Polymer Sirolimus-Eluting Stent: Randomized Substudy of the I-LOVE-IT 2 Trial. | LitMetric

Six Versus 12 Months of Dual Antiplatelet Therapy After Implantation of Biodegradable Polymer Sirolimus-Eluting Stent: Randomized Substudy of the I-LOVE-IT 2 Trial.

Circ Cardiovasc Interv

From the Department of Cardiology, General Hospital of Shenyang Military Region, Shenyang, China (Y.H., K.X., Q.J., J.L.); Catheterization Laboratory, Fu Wai Hospital, National Center for Cardiovascular Diseases, Beijing, China (B.X., C.G.); Department of Cardiology, Fu Wai Hospital, National Center for Cardiovascular Diseases, Beijing, China (Y.Y.); Department of Cardiology, Affiliated Tangdu Hospital of the Fourth Military Medical University, Xi'an, China (Q.Z.); Department of Cardiology, Fourth Affiliated Hospital of Haerbin Medical University, Haerbin, China (Xueqi Li); Department of Cardiology, Affiliated Changhai Hospital of the Second Military Medical University, Shanghai, China (Xianxian Zhao); Department of Cardiology, Affiliated Xijing Hospital of the Fourth Military Medical University, Xi'an, China (H.W.); Department of Cardiology, Jilin University First Hospital, Changchun, China (Xuezhong Zhao); Department of Cardiology, General Hospital of Jinan Military Region, Jinan, China (Xiaoyan Li); Department of Cardiology, Pingdu People's Hospital, Pingdu, China (P.Y.); Department of Cardiology, NO. 463 Hospital of PLA, Shenyang, China (H.Z.); Department of Cardiology, Xinxiang Central Hospital, Xinxiang, China (Z.W.); Department of Cardiology, NO. 252 Hospital of PLA, Baoding, China (X.C.); Department of Cardiology, Cangzhou Central Hospital, Cangzhou, China (J.Z.); Department of Cardiology, Shengjing Hospital, Shenyang, China (W.P.); and The Zena and Michael A. Wiener Cardiovascular Institute, Interventional Cardiovascular Research and Clinical Trials Center, Mount Sinai Medical Center, New York (G.D.D.).

Published: February 2016

Background: There are no reports on a large-scale randomized trial exploring optimal dual antiplatelet therapy (DAPT) duration after biodegradable polymer sirolimus-eluting stent implantation. We sought to report the outcomes of a randomized substudy of the prospective Evaluate Safety and Effectiveness of the Tivoli DES and the Firebird DES for Treatment of Coronary Revascularization (I-LOVE-IT 2) trial.

Methods And Results: In the prospective noninferiority randomized I-LOVE-IT 2 trial, 1829 patients allocated to the biodegradable polymer sirolimus-eluting stent group were also randomized to receive either 6-month (n=909) or 12-month DAPT (n=920). The primary end points of this noninferiority substudy were 12-month target lesion failure (composite of cardiac death, target vessel myocardial infarction or clinically indicated target lesion revascularization), and the major secondary end points were 12-month net adverse clinical and cerebral events (composite of all-cause death, all myocardial infarction, stroke, or major bleeding [Bleeding Academic Research Consortium type ≥3]). The 12-month target lesion failure in 6-month DAPT group was comparable with the 12-month DAPT group (6.8% versus 5.9%; difference and 95% confidence interval, 0.87% [-1.37% to 3.11%], P for noninferiority=0.0065). Further follow-up at 18 months showed that incidence of target lesion failure and net adverse clinical and cerebral events were similar between the 2 groups (7.5% versus 6.3%, log-rank P=0.32; 7.8% versus 7.3%, log-rank P=0.60; respectively), as well as their individual end point components.

Conclusions: This study indicated noninferiority in safety and efficacy of 6-month versus 12-month DAPT after implantation of a novel biodegradable polymer sirolimus-eluting stent.

Clinical Trial Registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01681381.

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Source
http://dx.doi.org/10.1161/CIRCINTERVENTIONS.115.003145DOI Listing

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