Randomized Comparison of the Nobori Biolimus A9-Eluting Coronary Stent With the Taxus Liberte Paclitaxel-Eluting Coronary Stent in Patients With Stenosis in Native Coronary Arteries The NOBORI 1 Trial - Phase 2

被引:134
|
作者
Chevalier, Bernard [1 ,9 ]
Silber, Sigmund [2 ]
Park, Seung-Jung [3 ]
Garcia, Eulogio
Schuler, Gerhard [4 ]
Suryapranata, Harry [5 ]
Koolen, Jacques [6 ]
Hauptmann, Karl E. [7 ]
Wijns, William [8 ]
Morice, Marie-Claude [9 ]
Carrie, Didier [10 ]
van Es, Gerrit-Anne [11 ]
Nagai, Hirofumi [12 ]
Detiege, Danny [12 ]
Paunovic, Dragica [12 ]
Serruys, Patrick W. [13 ]
机构
[1] Inst Cardiovasc Paris Sud, Massy Quincy, France
[2] Kardiol Gemeinschaftspraxis & Praxisklin, Munich, Germany
[3] Asan Med Ctr, Dept Med, Seoul, South Korea
[4] Univ Leipzig, Ctr Heart, Leipzig, Germany
[5] Isala Clin, Zwolle, Netherlands
[6] Catharina Hosp, Dept Cardiol, Eindhoven, Netherlands
[7] Krankenhaus Barmherzigen Bruder, Trier, Germany
[8] Ctr Cardiovasc, Aalst, Belgium
[9] Inst Cardiovasc Paris Sud, F-91300 Massy, France
[10] CHU Rangueil, Dept Cardiol, F-31054 Toulouse, France
[11] Cardialysis, Rotterdam, Netherlands
[12] Terumo Europe, Leuven, Belgium
[13] Erasmus Univ, Thoraxctr, NL-3000 DR Rotterdam, Netherlands
关键词
drug eluting stent; angioplasty; Biolimus A9; paclitaxel; randomized trial; INTRAVASCULAR ULTRASOUND; DOUBLE-BLIND; END-POINTS; THROMBOSIS; IMPLANTATION; POLYMER; DISEASE; LESIONS; HUMANS; REVASCULARIZATION;
D O I
10.1161/CIRCINTERVENTIONS.108.823443
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - The newly developed Nobori coronary stent coated with a bioresorbable polymer, polylactic acid, and the antiproliferative agent Biolimus A9 has the potential to reduce restenosis by suppressing neointima formation. Methods and Results - We conducted a randomized (2:1), controlled trial comparing the Biolimus A9-eluting stent Nobori and the paclitaxel-eluting stent Taxus Liberte, in 243 patients (153 Nobori and 90 Taxus) at 29 centers in Europe, Asia, and Australia. Patients with previously untreated lesions in up to 2 native coronary arteries were considered for enrollment. The primary end point was in-stent late loss at 9 months, whereas secondary end points included other quantitative coronary angiography parameters, such as in-segment late loss and the rate of restenosis as well as key intravascular ultrasound parameters. Clinical secondary end points were stent thrombosis and composite of major adverse cardiac events comprising death, myocardial infarction, and target vessel revascularization. At 9 months, the in-stent late loss was significantly lower in the Nobori group compared with the Taxus group (0.11 +/- 0.30 mm versus 0.32 +/- 0.50 mm) reaching both the primary hypothesis of noninferiority of Nobori stent versus Taxus Liberte stent (P < 0.001) and the secondary hypothesis of superiority (P=0.001). This finding was confirmed by a significant reduction in binary restenosis from 6.2% in Taxus to 0.7% in Nobori (P=0.02) and neointimal volume obstruction, detected by intravascular ultrasound, from 5.5 +/- 7.2% in Taxus to 1.8 +/- 5.2% in Nobori (P=0.01). The major adverse cardiac events rate was 4.6% in the Nobori and 5.6% in the Taxus cohort of patients. The stent thrombosis rate was 0% in the Nobori arm and 4.4% in the Taxus arm. Conclusions - The NOBORI 1 clinical trial confirmed its primary hypothesis-noninferiority of the Nobori Biolimus A9-eluting stent versus the Taxus Liberte stent in reducing neointimal proliferation. Both stents showed a low major adverse cardiac events rate in the studied population. (Circ Cardiovasc Intervent. 2009;2:188-195.)
引用
收藏
页码:188 / U57
页数:12
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