Literature DB >> 17174180

Comparison of zotarolimus-eluting and sirolimus-eluting stents in patients with native coronary artery disease: a randomized controlled trial.

David E Kandzari1, Martin B Leon, Jeffrey J Popma, Peter J Fitzgerald, Charles O'Shaughnessy, Michael W Ball, Mark Turco, Robert J Applegate, Paul A Gurbel, Mark G Midei, Sejal S Badre, Laura Mauri, Kweli P Thompson, LeRoy A LeNarz, Richard E Kuntz.   

Abstract

OBJECTIVES: This trial examined the relative clinical efficacy, angiographic outcomes, and safety of zotarolimus-eluting coronary stents (ZES) with a phosphorylcholine polymer versus sirolimus-eluting stents (SES).
BACKGROUND: Whether a cobalt-based alloy stent coated with the novel antiproliferative agent, zotarolimus, and a phosphorylcholine polymer may provide similar angiographic and clinical benefit compared with SES is undetermined.
METHODS: A prospective, multicenter, 3:1 randomized trial was conducted to evaluate the safety and efficacy of ZES (n = 323) relative to SES (n = 113) in 436 patients undergoing elective percutaneous revascularization of de novo native coronary lesions with reference vessel diameters between 2.5 mm and 3.5 mm and lesion length > or =14 mm and < or =27 mm. The primary end point was 8-month angiographic in-segment late lumen loss.
RESULTS: Angiographic in-segment late lumen loss was significantly higher among patients treated with ZES compared with SES (0.34 +/- 0.44 mm vs. 0.13 +/- 0.32 mm, respectively; p < 0.001). In-hospital major adverse cardiac events were significantly lower among patients treated with ZES (0.6% vs. 3.5%, p = 0.04). In-segment binary angiographic restenosis was also higher in the ZES cohort (11.7% vs. 4.3%, p = 0.04). Total (clinically and non-clinically driven) target lesion revascularization rates at 9 months were 9.8% and 3.5% for the ZES and SES groups, respectively (p = 0.04). However, neither clinically driven target lesion revascularization (6.3% zotarolimus vs. 3.5% sirolimus, p = 0.34) nor target vessel failure (12.0% zotarolimus vs. 11.5% sirolimus, p = 1.0) differed significantly.
CONCLUSIONS: Compared with SES, treatment with a phosphorylcholine polymer-based ZES is associated with significantly higher late lumen loss and binary restenosis at 8-month angiographic follow-up. (The Endeavor III CR; http://clinicaltrials.gov/ct/show/NCT00265668?order=1?).

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Year:  2006        PMID: 17174180     DOI: 10.1016/j.jacc.2006.08.035

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  52 in total

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2.  Revascularization treatment in patients with coronary artery disease.

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Authors:  Svea Petersen; Janine Hussner; Thomas Reske; Niels Grabow; Volkmar Senz; Robert Begunk; Daniela Arbeiter; Heyo K Kroemer; Klaus-Peter Schmitz; Henriette E Meyer zu Schwabedissen; Katrin Sternberg
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Authors:  Ashwin B Mehta; Praveen Chandra; Jamshed Dalal; Prabhakar Shetty; Devang Desai; K Chocklingam; Jayesh Prajapati; Pramod Kumar; Vilas Magarkar; Apurva Vasawada; B K Goyal; Viveka Kumar; V Suryaprakash Rao; Ramesh Babu; Pritesh Parikh; Upendra Kaul; Aruna Patil; Tushar Mhetre; Hrishikesh Rangnekar
Journal:  Indian Heart J       Date:  2013-09-23

5.  Zotarolimus-eluting stent utilization in small-vessel coronary artery disease (ZEUS).

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Review 9.  Small coronary vessel angioplasty: outcomes and technical considerations.

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10.  Optical coherence tomography evaluation of zotarolimus-eluting stents at 9-month follow-up: comparison with sirolimus-eluting stents.

Authors:  J-S Kim; I-K Jang; J-S Kim; T H Kim; M Takano; T Kume; N W Hur; Y-G Ko; D Choi; M-K Hong; Y Jang
Journal:  Heart       Date:  2009-06-16       Impact factor: 5.994

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