Comparison of a novel biodegradable polymer sirolimus-eluting stent With a durable polymer everolimus-eluting stent results of the randomized BIOFLOW-II trial
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Windecker, Stephan
Department of Cardiology, Bern University Hospital, Bern, Switzerland
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Haude, Michael
Städtische Kliniken Neuss, Lukaskrankenhaus GmbH, Neuss, Germany
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Neumann, Franz-Josef
Universitäts-Herzzentrum Freiburg–Bad Krozingen, Bad Krozingen, Germany
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Stangl, karl
Charité-Campus Mitte, Berlin, Germany
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Witzenbichler, Bernhard
Charité Campus Benjamin Franklin, Berlin, Germany
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Slagboom, Ton
Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands
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Sabaté, Manel
Hospital Clínic, Thorax Institute, Barcelona, Spain - IDIBAPS, University of Barcelona, Barcelona, Spain
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Goicolea, Javier
Hospital Puerta de Hierro, Madrid, Spain
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Barragan, Paul
Polyclinique les Fleurs, Ollioules, France
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Cook, Stéphane
Hospital and University of Fribourg, Switzerland
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Piot, Christophe
University of Montpellier, Montpellier, France
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Richardt, Gert
Segeberger Kliniken, Bad Segeberg, Germany
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Merkely, Béla
Semmelweis University Heart and Vascular Center, Budapest, Hungary
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Schneider, Henrik
Universitätsklinikum Rostock, Rostock, Germany
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Bilger, Johannes
Klinikum Nürnberg Süd, Nürnberg, Germany
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Erne, Paul
Lucerne Canton Hospital, Lucerne, Switzerland
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Waksman, Ron
MedStar Health Research Institute, Washington, DC
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Zaugg, Serge
Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland
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Jüni, Peter
Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland
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Lefèvre, Thierry
ICPS, Massy, France
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Published in:
- Circulation: Cardiovascular Interventions. - 2015, vol. 8, no. 2, p. e001441
English
Background—Biodegradable polymers for release of antiproliferative drugs from drug-eluting stents aim to improve vascular healing. We assessed noninferiority of a novel ultrathin strut drug-eluting stent releasing sirolimus from a biodegradable polymer (Orsiro, O-SES) compared with the durable polymer Xience Prime everolimus-eluting stent (X-EES) in terms of the primary end point in-stent late lumen loss at 9 months.Methods and Results—A total of 452 patients were randomly assigned 2:1 to treatment with O-SES (298 patients, 332 lesions) or X-EES (154 patients, 173 lesions) in a multicenter, noninferiority trial. The primary end point was in-stent late loss at 9 months. O-SES was noninferior to X-EES for the primary end point (0.10±0.32 versus 0.11±0.29 mm; difference=0.00063 mm; 95% confidence interval, −0.06 to 0.07; Pnoninferiority<0.0001). Clinical outcome showed similar rates of target-lesion failure at 1 year (O-SES 6.5% versus X-EES 8.0%; hazard ratio=0.82; 95% confidence interval, 0.40–1.68; log-rank test: P=0.58) without cases of stent thrombosis. A subgroup of patients (n=55) underwent serial optical coherence tomography at 9 months, which demonstrated similar neointimal thickness among lesions allocated to O-SES and X-EES (0.10±0.04 mm versus 0.11±0.04 mm; −0.01 [−0.04, −0.01]; P=0.37). Another subgroup of patients (n=56) underwent serial intravascular ultrasound at baseline and 9 months indicating a potential difference in neointimal area at follow-up (O-SES, 0.16±0.33 mm² versus X-EES, 0.43±0.56 mm²; P=0.04).Conclusions—Compared with durable polymer X-EES, novel biodegradable polymer–based O-SES was found noninferior for the primary end point in-stent late lumen loss at 9 months. Clinical event rates were comparable without cases of stent thrombosis throughout 1 year of follow-up.Clinical Trial Registration—URL: http://www.clinicaltrials.gov. Unique identifier: NCT01356888.
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Faculty
- Faculté des sciences et de médecine
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Department
- Médecine 3ème année
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Language
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Classification
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Pathology, clinical medicine
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License
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License undefined
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Identifiers
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Persistent URL
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https://folia.unifr.ch/unifr/documents/304427
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