TY - JOUR
T1 - 1-Year Clinical Outcomes of All-Comer Patients Treated With the Dual-Therapy COMBO Stent
T2 - Primary Results of the COMBO Collaboration
AU - MASCOT
AU - REMEDEE Registry Investigators
AU - de Winter, Robbert J.
AU - Chandrasekhar, Jaya
AU - Kalkman, Deborah N.
AU - Aquino, Melissa B.
AU - Woudstra, Pier
AU - Beijk, Marcel A.
AU - Sartori, Samantha
AU - Baber, Usman
AU - Tijssen, Jan G.
AU - Koch, Karel T.
AU - Dangas, George D.
AU - Colombo, Antonio
AU - Mehran, Roxana
AU - Ong, Tiong Kiam
AU - Lee, Michael
AU - Iniguez, Andres
AU - Rowland, Stephen
AU - Ghodsi, Newsha
AU - Marx, Steven
AU - DiStefano, Douglas
AU - Weinberger, Jesse
AU - Wong, Shing Chiu
AU - Darrow, Bruce
AU - Kaufman, David
AU - Milstein, Mark
AU - Chandrasekhar, Jaya
AU - Snyder, Clayton
AU - Franklin-Bond, Theresa
AU - Cha, Jin Young
AU - Vandertie, Lynn
AU - Whittaker, Emma
AU - Allen, Kate
AU - Vogel, Birgit
AU - Farhan, Serdar
AU - Sorrentino, Sabato
AU - Ge, Zhen
AU - Carlier, Marc
AU - Pourbaix, Suzanne
AU - Borisov, Borislav
AU - Atzev, Borislav
AU - Vasilev, Dobrin
AU - Christou, Christos
AU - Pešl, Ladislav
AU - Coufal, Zdeněk
AU - Kala, Petr
AU - Jeřábek, Petr
AU - Hájek, Petr
AU - Schee, Alexander
AU - Ondrejcak, Roman
AU - Rozsíval, Vladimír
N1 - Publisher Copyright:
© 2018
PY - 2018/10/8
Y1 - 2018/10/8
N2 - Objectives: The aim of this study was to evaluate 1-year clinical safety and efficacy of the dual-therapy COMBO stent in a large, all-comers patient-level pooled cohort. Background: The COMBO stent (OrbusNeich Medical, Fort Lauderdale, Florida) is a novel stent with abluminal sirolimus elution from a biodegradable polymer and a luminal pro-healing anti-CD34+ antibody layer, which attracts circulating endothelial progenitor cells. These endothelial progenitor cells can quickly mature into normal endothelium, providing rapid endothelialization. Methods: The MASCOT (Multinational Abluminal Sirolimus Coated biO-engineered stenT) (N = 2,614, 61 global sites) and REMEDEE (Randomized study to Evaluate the safety and effectiveness of an abluMinal sirolimus coatED bio-Engineered StEnt Post Market Registry) (N = 1,000, 9 European sites) registries are 2 prospective, multicenter studies evaluating clinical outcomes after attempted COMBO stent placement in all-comer patients undergoing percutaneous coronary intervention. In this patient-level pooled analysis we analyzed 1-year target lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction, or clinically driven target lesion revascularization. Furthermore, we determined predictors of 1-year TLF. Results: A total of 3,614 patients (63.5 ± 11.2 years of age; 23.8% women) were included in this analysis. The prevalence of diabetes mellitus was 29.3%, and 54.3% patients presented with acute coronary syndrome. The primary endpoint of 1-year TLF occurred in 140 (3.9%) patients, with incidence of cardiac death in 1.6%, target vessel myocardial infarction in 1.2%, clinically driven target lesion revascularization in 2.2%, and definite stent thrombosis in 0.5% patients. Insulin-treated diabetes mellitus, chronic renal failure, and American College of Cardiology/American Heart Association lesion type B2/C were independent predictors of 1-year TLF. Conclusions: In this large patient-level pooled analysis of patients treated with the dual-therapy COMBO stent excellent results at 1-year were observed.
AB - Objectives: The aim of this study was to evaluate 1-year clinical safety and efficacy of the dual-therapy COMBO stent in a large, all-comers patient-level pooled cohort. Background: The COMBO stent (OrbusNeich Medical, Fort Lauderdale, Florida) is a novel stent with abluminal sirolimus elution from a biodegradable polymer and a luminal pro-healing anti-CD34+ antibody layer, which attracts circulating endothelial progenitor cells. These endothelial progenitor cells can quickly mature into normal endothelium, providing rapid endothelialization. Methods: The MASCOT (Multinational Abluminal Sirolimus Coated biO-engineered stenT) (N = 2,614, 61 global sites) and REMEDEE (Randomized study to Evaluate the safety and effectiveness of an abluMinal sirolimus coatED bio-Engineered StEnt Post Market Registry) (N = 1,000, 9 European sites) registries are 2 prospective, multicenter studies evaluating clinical outcomes after attempted COMBO stent placement in all-comer patients undergoing percutaneous coronary intervention. In this patient-level pooled analysis we analyzed 1-year target lesion failure (TLF), a composite of cardiac death, target vessel myocardial infarction, or clinically driven target lesion revascularization. Furthermore, we determined predictors of 1-year TLF. Results: A total of 3,614 patients (63.5 ± 11.2 years of age; 23.8% women) were included in this analysis. The prevalence of diabetes mellitus was 29.3%, and 54.3% patients presented with acute coronary syndrome. The primary endpoint of 1-year TLF occurred in 140 (3.9%) patients, with incidence of cardiac death in 1.6%, target vessel myocardial infarction in 1.2%, clinically driven target lesion revascularization in 2.2%, and definite stent thrombosis in 0.5% patients. Insulin-treated diabetes mellitus, chronic renal failure, and American College of Cardiology/American Heart Association lesion type B2/C were independent predictors of 1-year TLF. Conclusions: In this large patient-level pooled analysis of patients treated with the dual-therapy COMBO stent excellent results at 1-year were observed.
KW - drug-eluting stent(s)
KW - endothelial progenitor cell anti-CD34+ antibody
KW - percutaneous coronary intervention
KW - stent healing
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U2 - 10.1016/j.jcin.2018.04.038
DO - 10.1016/j.jcin.2018.04.038
M3 - Article
C2 - 30286855
AN - SCOPUS:85053759376
SN - 1936-8798
VL - 11
SP - 1969
EP - 1978
JO - JACC: Cardiovascular Interventions
JF - JACC: Cardiovascular Interventions
IS - 19
ER -