A Novel Paclitaxel-Eluting Stent With an Ultrathin Abluminal Biodegradable Polymer 9-Month Outcomes With the JACTAX HD Stent

被引:36
作者
Grube, Eberhard [1 ]
Schofer, Joachim [2 ]
Hauptmann, Karl E. [3 ]
Nickenig, Georg [4 ]
Curzen, Nicholas [5 ]
Allocco, Dominic J. [6 ]
Dawkins, Keith D. [6 ]
机构
[1] HELIOS Heart Ctr, Siegburg, Germany
[2] Cardiovasc Med Care Ctr, Hamburg, Germany
[3] Krankenhaus Barmherzigen Bruder, Trier, Germany
[4] Univ Klinikum Bonn, Med Klin & Poliklin 2, Bonn, Germany
[5] Southampton Univ Hosp, Southampton, Hants, England
[6] Boston Sci Corp, Natick, MA USA
关键词
CORONARY-ARTERY-DISEASE; OPTICAL COHERENCE TOMOGRAPHY; RANDOMIZED-TRIAL; FOLLOW-UP; NEOINTIMAL COVERAGE; LESIONS; IMPLANTATION; RESTENOSIS; THROMBOSIS; REDUCTION;
D O I
10.1016/j.jcin.2009.12.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The JACTAX HD trial ("JACTAX" Trial Drug Eluting Stent Trial) evaluated the safety and clinical performance of a novel JACTAX HD (Boston Scientific Corporation, Natick, Massachusetts) paclitaxel-eluting stent (PES) in de novo coronary lesions. Background The JACTAX HD (Boston Scientific) stent consists of a pre-crimped bare-metal Liberte (Boston Scientific) stent coated on its abluminal aspect with an ultrathin (<1 mu m) 1/1 mixture of biodegradable polylactide polymer and paclitaxel applied as discrete microdots (nominal totals of 9.2 mu g each of polymer and paclitaxel per 16-mm stent). Methods In this prospective, single-arm, multicenter, first-human-use study (n = 103), the primary end point of 9-month major adverse cardiac events (MACE) (cardiac death, myocardial infarction, ischemia-related target vessel revascularization) was compared with an objective performance criterion (OPC) of 17% (11% MACE based on TAXUS ATLAS [TAXUS Liberte-SR Stent for the Treatment of de Novo Coronary Artery Lesions) trial results plus a pre-specified noninferiority margin of 6%). Results The composite primary end point occurred in 7.8% of JACTAX HD patients with an upper 1-sided 95% confidence limit of 13.6%, thus meeting the pre-specified criteria for noninferiority. There was no death, Q-wave myocardial infarction, or stent thrombosis through 9 months. In-stent late loss was 0.33 +/- 0.45 mm, with an in-stent binary restenosis of 5.2% and net volume obstruction by intravascular ultrasound of 11.4 +/- 11.2%. Conclusions The JACTAX HD stent with an abluminal biodegradable polymer showed 9-month MACE, in-stent late loss, restenosis, and net volume obstruction comparable to that observed with the TAXUS Liberte (Boston Scientific) stent coated with a conformal durable polymer. Further studies are underway to better evaluate the potential of this new PES design, which might allow for more rapid endothelialization and improved vessel healing. ("JACTAX" Trial Drug Eluting Stent Trial; NCT00754728) (J Am Coll Cardiol Intv 2010;3:431-8) (C) 2010 by the American College of Cardiology Foundation
引用
收藏
页码:431 / 438
页数:8
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