10-Year Outcomes From a Randomized Trial of Polymer-Free Versus Durable Polymer Drug-Eluting Coronary Stents.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
14 07 2020
Historique:
received: 23 03 2020
revised: 10 05 2020
accepted: 10 05 2020
entrez: 11 7 2020
pubmed: 11 7 2020
medline: 13 1 2021
Statut: ppublish

Résumé

Outcome data after extended long-term follow-up of patients with coronary artery disease treated with drug-eluting stents (DES) in randomized clinical trials are scant. Performance differences among devices may be expected to emerge over time depending on whether stenting is done with polymer-free or durable polymer DES. This study assessed the 10-year outcomes of patients enrolled in the ISAR-TEST-5 (Test Efficacy of Sirolimus- and Probucol-Eluting Versus Zotarolimus-Eluting Stents) trial. A total of 3,002 patients were randomized to treatment with either polymer-free sirolimus- and probucol-eluting stents (n = 2,002) or durable polymer zotarolimus-eluting stents (n = 1,000). The primary endpoint was the composite of cardiac death, target vessel-related myocardial infarction, or target lesion revascularization (a device-oriented composite endpoint [DOCE]). Additional endpoints of interest were the patient-oriented composite endpoint (POCE), including all-cause death, any myocardial infarction, or any revascularization; individual components of the composite endpoints; and definite or probable stent thrombosis. The median age of the patients at randomization was 67.8 years. At 10 years, 63.9% of patients were alive. The rates of DOCE and POCE were high in both groups with no difference in the incidence between polymer-free sirolimus- and probucol-eluting stents and durable polymer zotarolimus-eluting stents (DOCE: 43.8% vs. 43.0%, respectively; hazard ratio: 1.01; 95% confidence interval [CI]: 0.89 to 1.14; p = 0.90; POCE: 66.2% vs. 67.7%, respectively; hazard ratio: 0.94; 95% CI: 0.86 to 1.04; p = 0.22). The rates of the individual components of the composite endpoints were comparable in both groups. The incidence of definite/probable stent thrombosis over 10 years was low and comparable in both groups (1.6% vs. 1.9%; hazard ratio: 0.85; 95% CI: 0.46 to 1.54; p = 0.58). At 10 years, there were no measurable differences in outcomes between patients treated with polymer-free versus durable polymer DES. The incidence of stent thrombosis was low and comparable in both groups. High overall adverse clinical event rates were observed during extended follow-up. (Test Efficacy of Sirolimus- and Probucol-Eluting Versus Zotarolimus-Eluting Stents [ISAR-TEST-5]; NCT00598533).

Sections du résumé

BACKGROUND
Outcome data after extended long-term follow-up of patients with coronary artery disease treated with drug-eluting stents (DES) in randomized clinical trials are scant.
OBJECTIVES
Performance differences among devices may be expected to emerge over time depending on whether stenting is done with polymer-free or durable polymer DES. This study assessed the 10-year outcomes of patients enrolled in the ISAR-TEST-5 (Test Efficacy of Sirolimus- and Probucol-Eluting Versus Zotarolimus-Eluting Stents) trial.
METHODS
A total of 3,002 patients were randomized to treatment with either polymer-free sirolimus- and probucol-eluting stents (n = 2,002) or durable polymer zotarolimus-eluting stents (n = 1,000). The primary endpoint was the composite of cardiac death, target vessel-related myocardial infarction, or target lesion revascularization (a device-oriented composite endpoint [DOCE]). Additional endpoints of interest were the patient-oriented composite endpoint (POCE), including all-cause death, any myocardial infarction, or any revascularization; individual components of the composite endpoints; and definite or probable stent thrombosis.
RESULTS
The median age of the patients at randomization was 67.8 years. At 10 years, 63.9% of patients were alive. The rates of DOCE and POCE were high in both groups with no difference in the incidence between polymer-free sirolimus- and probucol-eluting stents and durable polymer zotarolimus-eluting stents (DOCE: 43.8% vs. 43.0%, respectively; hazard ratio: 1.01; 95% confidence interval [CI]: 0.89 to 1.14; p = 0.90; POCE: 66.2% vs. 67.7%, respectively; hazard ratio: 0.94; 95% CI: 0.86 to 1.04; p = 0.22). The rates of the individual components of the composite endpoints were comparable in both groups. The incidence of definite/probable stent thrombosis over 10 years was low and comparable in both groups (1.6% vs. 1.9%; hazard ratio: 0.85; 95% CI: 0.46 to 1.54; p = 0.58).
CONCLUSIONS
At 10 years, there were no measurable differences in outcomes between patients treated with polymer-free versus durable polymer DES. The incidence of stent thrombosis was low and comparable in both groups. High overall adverse clinical event rates were observed during extended follow-up. (Test Efficacy of Sirolimus- and Probucol-Eluting Versus Zotarolimus-Eluting Stents [ISAR-TEST-5]; NCT00598533).

Identifiants

pubmed: 32646563
pii: S0735-1097(20)35314-6
doi: 10.1016/j.jacc.2020.05.026
pii:
doi:

Substances chimiques

Polymers 0
zotarolimus H4GXR80IZE
Sirolimus W36ZG6FT64

Banques de données

ClinicalTrials.gov
['NCT00598533']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

146-158

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Sebastian Kufner (S)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany. Electronic address: Sebastian.Kufner@gmx.de.

Maximilian Ernst (M)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Salvatore Cassese (S)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Michael Joner (M)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany; German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.

Katharina Mayer (K)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Roisin Colleran (R)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Tobias Koppara (T)

Klinik und Poliklinik Innere Medizin I (Kardiologie, Angiologie und Pneumologie), Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Erion Xhepa (E)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Tobias Koch (T)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Jens Wiebe (J)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Tareq Ibrahim (T)

Klinik und Poliklinik Innere Medizin I (Kardiologie, Angiologie und Pneumologie), Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Massimiliano Fusaro (M)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.

Karl-Ludwig Laugwitz (KL)

German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany; Klinik und Poliklinik Innere Medizin I (Kardiologie, Angiologie und Pneumologie), Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

Heribert Schunkert (H)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany; German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.

Adnan Kastrati (A)

Deutsches Herzzentrum München, Technische Universität München, Munich, Germany; German Center for Cardiovascular Research, partner site Munich Heart Alliance, Munich, Germany.

Robert A Byrne (RA)

Dublin Cardiovascular Research Institute, Mater Private Hospital, Dublin, Ireland; School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons in Ireland, Dublin, Ireland.

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Classifications MeSH