New-generation drug-eluting stents for left main coronary artery disease according to the EXCEL trial enrollment criteria: Insights from the all-comers, international, multicenter DELTA-2 registry.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 01 10 2018
revised: 28 11 2018
accepted: 03 12 2018
pubmed: 1 1 2019
medline: 18 12 2019
entrez: 1 1 2019
Statut: ppublish

Résumé

Percutaneous coronary intervention (PCI) has been established as an alternative treatment option to coronary artery by-pass graft (CABG) surgery in patients with left main coronary artery disease (LMCAD). Whether the findings of randomized controlled trials are applicable to a real-world patient population is unclear. We compared the outcomes of PCI with new-generation DES in the all-comer, international, multicenter DELTA-2 registry retrospectively evaluating mid-term clinical outcomes with the historical CABG cohort enrolled in the DELTA-1 registry according to the EXCEL key inclusion or exclusion criteria. The primary endpoint was the composite of death, myocardial infarction, or stroke at the median time of follow-up time of 501 days. The consistency of the effect of DELTA-2 PCI versus DELTA-1 CABG according to the EXCEL enrollment criteria was tested using propensity score-adjusted Cox regression models. Out of 3986 patients enrolled in the DELTA-2 PCI registry, 2418 were EXCEL candidates and 1568 were not EXCEL candidates. The occurrence of the primary endpoint was higher among non-EXCEL candidates compared with EXCEL candidates (15.4% vs. 6.9%; hazard ratio 2.52; 95% confidence interval 2.00-3.16; p < 0.001). Among 901 patients enrolled in the historical DELTA-1 CABG cohort, 471 were EXCEL candidates and 430 were not EXCEL candidates. When comparing the DELTA-2 PCI with the DELTA-1 CABG cohort, the occurrence of the primary endpoint was lower in the PCI group compared with the historical CABG cohort among EXCEL candidates (6.9% vs. 10.7%; adjusted hazard ratio: 0.65; 95% confidence interval: 0.45-0.92), while no significant difference was observed among non-EXCEL candidates (15.4% vs. 12.5%; adjusted hazard ratio: 0.94; 95% confidence interval: 0.67-1.33) with evidence of statistical interaction (adjusted interaction p-value = 0.002). In a real-world population, PCI can be selected more favorably as an alternative to CABG in patients fulfilling the enrollment criteria of the EXCEL trial.

Sections du résumé

BACKGROUND
Percutaneous coronary intervention (PCI) has been established as an alternative treatment option to coronary artery by-pass graft (CABG) surgery in patients with left main coronary artery disease (LMCAD). Whether the findings of randomized controlled trials are applicable to a real-world patient population is unclear.
METHODS
We compared the outcomes of PCI with new-generation DES in the all-comer, international, multicenter DELTA-2 registry retrospectively evaluating mid-term clinical outcomes with the historical CABG cohort enrolled in the DELTA-1 registry according to the EXCEL key inclusion or exclusion criteria. The primary endpoint was the composite of death, myocardial infarction, or stroke at the median time of follow-up time of 501 days. The consistency of the effect of DELTA-2 PCI versus DELTA-1 CABG according to the EXCEL enrollment criteria was tested using propensity score-adjusted Cox regression models.
RESULTS
Out of 3986 patients enrolled in the DELTA-2 PCI registry, 2418 were EXCEL candidates and 1568 were not EXCEL candidates. The occurrence of the primary endpoint was higher among non-EXCEL candidates compared with EXCEL candidates (15.4% vs. 6.9%; hazard ratio 2.52; 95% confidence interval 2.00-3.16; p < 0.001). Among 901 patients enrolled in the historical DELTA-1 CABG cohort, 471 were EXCEL candidates and 430 were not EXCEL candidates. When comparing the DELTA-2 PCI with the DELTA-1 CABG cohort, the occurrence of the primary endpoint was lower in the PCI group compared with the historical CABG cohort among EXCEL candidates (6.9% vs. 10.7%; adjusted hazard ratio: 0.65; 95% confidence interval: 0.45-0.92), while no significant difference was observed among non-EXCEL candidates (15.4% vs. 12.5%; adjusted hazard ratio: 0.94; 95% confidence interval: 0.67-1.33) with evidence of statistical interaction (adjusted interaction p-value = 0.002).
CONCLUSIONS
In a real-world population, PCI can be selected more favorably as an alternative to CABG in patients fulfilling the enrollment criteria of the EXCEL trial.

Identifiants

pubmed: 30595357
pii: S0167-5273(18)35846-7
doi: 10.1016/j.ijcard.2018.12.003
pii:
doi:

Types de publication

Journal Article Multicenter Study Observational Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

30-37

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2018 Elsevier B.V. All rights reserved.

Auteurs

Akihito Tanaka (A)

Interventional Cardiology Unit, San Raffaele Scientific Institute, Milan, Italy.

Gennaro Giustino (G)

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.

Ieva Briede (I)

Pauls Stradins Clinical University Hospital, University of Latvia, Riga, Latvia.

Fadi J Sawaya (FJ)

Hopital privé Jacques Cartier, Ramsay Générale de Santé, Massy, France.

Joost Daemen (J)

Erasmus Medical Center, Thoraxcenter, Rotterdam, the Netherlands.

Hiroyoshi Kawamoto (H)

Interventional Cardiology Unit, New Tokyo Hospital, Chiba, Japan.

Emanuele Meliga (E)

Department of Cardiology, Mauriziano Hospital, Turin, Italy.

Fabrizio D'Ascenzo (F)

Department of Internal Medicine, Division of Cardiology, University of Turin, Città della Salute e della Scienza, Turin, Italy.

Enrico Cerrato (E)

San Luigi Gonzaga University Hospital, Orbassano and Infermi Hospital, Rivoli, Turin, Italy.

Giulio G Stefanini (GG)

Department of Biomedical Sciences, Humanitas University, Rozzano, Milan, Italy.

Davide Capodanno (D)

C.A.S.T., P.O. Gaspare Rodolico, Azienda-Ospedaliero Universitaria "Policlinico-Vittorio Emanuele", Catania, Italy.

Andrea Mangiameli (A)

Clinique Pasteur, Toulouse, France.

Christian Templin (C)

University Hospital of Zurich, Zurich, Switzerland.

Andrejs Erglis (A)

Pauls Stradins Clinical University Hospital, University of Latvia, Riga, Latvia.

Marie Claude Morice (MC)

Hopital privé Jacques Cartier, Ramsay Générale de Santé, Massy, France.

Roxana Mehran (R)

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.

Nicolas M Van Mieghem (NM)

Erasmus Medical Center, Thoraxcenter, Rotterdam, the Netherlands.

Sunao Nakamura (S)

Interventional Cardiology Unit, New Tokyo Hospital, Chiba, Japan.

Mauro De Benedictis (M)

Department of Cardiology, Mauriziano Hospital, Turin, Italy.

Marco Pavani (M)

Department of Internal Medicine, Division of Cardiology, University of Turin, Città della Salute e della Scienza, Turin, Italy.

Ferdinando Varbella (F)

San Luigi Gonzaga University Hospital, Orbassano and Infermi Hospital, Rivoli, Turin, Italy.

Marco Pisaniello (M)

Department of Biomedical Sciences, Humanitas University, Rozzano, Milan, Italy.

Samin K Sharma (SK)

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.

Corrado Tamburino (C)

C.A.S.T., P.O. Gaspare Rodolico, Azienda-Ospedaliero Universitaria "Policlinico-Vittorio Emanuele", Catania, Italy.

Didier Tchetche (D)

Clinique Pasteur, Toulouse, France.

Antonio Colombo (A)

Interventional Cardiology Unit, San Raffaele Scientific Institute, Milan, Italy.

Alaide Chieffo (A)

Interventional Cardiology Unit, San Raffaele Scientific Institute, Milan, Italy. Electronic address: chieffo.alaide@hsr.it.

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