Percutaneous coronary angioplasty versus coronary artery bypass grafting in the treatment of unprotected left main stenosis: updated 5-year outcomes from the randomised, non-inferiority NOBLE trial.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
18 01 2020
Historique:
received: 23 09 2019
revised: 11 11 2019
accepted: 12 11 2019
pubmed: 28 12 2019
medline: 6 2 2020
entrez: 28 12 2019
Statut: ppublish

Résumé

Percutaneous coronary intervention (PCI) is increasingly used in revascularisation of patients with left main coronary artery disease in place of the standard treatment, coronary artery bypass grafting (CABG). The NOBLE trial aimed to evaluate whether PCI was non-inferior to CABG in the treatment of left main coronary artery disease and reported outcomes after a median follow-up of 3·1 years. We now report updated 5-year outcomes of the trial. The prospective, randomised, open-label, non-inferiority NOBLE trial was done at 36 hospitals in nine northern European countries. Patients with left main coronary artery disease requiring revascularisation were enrolled and randomly assigned (1:1) to receive PCI or CABG. The primary endpoint was major adverse cardiac or cerebrovascular events (MACCE), a composite of all-cause mortality, non-procedural myocardial infarction, repeat revascularisation, and stroke. Non-inferiority of PCI to CABG was defined as the upper limit of the 95% CI of the hazard ratio (HR) not exceeding 1·35 after 275 MACCE had occurred. Secondary endpoints included all-cause mortality, non-procedural myocardial infarction, and repeat revascularisation. Outcomes were analysed in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT01496651. Between Dec 9, 2008, and Jan 21, 2015, 1201 patients were enrolled and allocated to PCI (n=598) or CABG (n=603), with 17 subsequently lost to early follow-up. 592 patients in each group were included in this analysis. At a median of 4·9 years of follow-up, the predefined number of events was reached for adequate power to assess the primary endpoint. Kaplan-Meier 5-year estimates of MACCE were 28% (165 events) for PCI and 19% (110 events) for CABG (HR 1·58 [95% CI 1·24-2·01]); the HR exceeded the limit for non-inferiority of PCI compared to CABG. CABG was found to be superior to PCI for the primary composite endpoint (p=0·0002). All-cause mortality was estimated in 9% after PCI versus 9% after CABG (HR 1·08 [95% CI 0·74-1·59]; p=0·68); non-procedural myocardial infarction was estimated in 8% after PCI versus 3% after CABG (HR 2·99 [95% CI 1·66-5·39]; p=0·0002); and repeat revascularisation was estimated in 17% after PCI versus 10% after CABG (HR 1·73 [95% CI 1·25-2·40]; p=0·0009). In revascularisation of left main coronary artery disease, PCI was associated with an inferior clinical outcome at 5 years compared with CABG. Mortality was similar after the two procedures but patients treated with PCI had higher rates of non-procedural myocardial infarction and repeat revascularisation. Biosensors.

Sections du résumé

BACKGROUND
Percutaneous coronary intervention (PCI) is increasingly used in revascularisation of patients with left main coronary artery disease in place of the standard treatment, coronary artery bypass grafting (CABG). The NOBLE trial aimed to evaluate whether PCI was non-inferior to CABG in the treatment of left main coronary artery disease and reported outcomes after a median follow-up of 3·1 years. We now report updated 5-year outcomes of the trial.
METHODS
The prospective, randomised, open-label, non-inferiority NOBLE trial was done at 36 hospitals in nine northern European countries. Patients with left main coronary artery disease requiring revascularisation were enrolled and randomly assigned (1:1) to receive PCI or CABG. The primary endpoint was major adverse cardiac or cerebrovascular events (MACCE), a composite of all-cause mortality, non-procedural myocardial infarction, repeat revascularisation, and stroke. Non-inferiority of PCI to CABG was defined as the upper limit of the 95% CI of the hazard ratio (HR) not exceeding 1·35 after 275 MACCE had occurred. Secondary endpoints included all-cause mortality, non-procedural myocardial infarction, and repeat revascularisation. Outcomes were analysed in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT01496651.
FINDINGS
Between Dec 9, 2008, and Jan 21, 2015, 1201 patients were enrolled and allocated to PCI (n=598) or CABG (n=603), with 17 subsequently lost to early follow-up. 592 patients in each group were included in this analysis. At a median of 4·9 years of follow-up, the predefined number of events was reached for adequate power to assess the primary endpoint. Kaplan-Meier 5-year estimates of MACCE were 28% (165 events) for PCI and 19% (110 events) for CABG (HR 1·58 [95% CI 1·24-2·01]); the HR exceeded the limit for non-inferiority of PCI compared to CABG. CABG was found to be superior to PCI for the primary composite endpoint (p=0·0002). All-cause mortality was estimated in 9% after PCI versus 9% after CABG (HR 1·08 [95% CI 0·74-1·59]; p=0·68); non-procedural myocardial infarction was estimated in 8% after PCI versus 3% after CABG (HR 2·99 [95% CI 1·66-5·39]; p=0·0002); and repeat revascularisation was estimated in 17% after PCI versus 10% after CABG (HR 1·73 [95% CI 1·25-2·40]; p=0·0009).
INTERPRETATION
In revascularisation of left main coronary artery disease, PCI was associated with an inferior clinical outcome at 5 years compared with CABG. Mortality was similar after the two procedures but patients treated with PCI had higher rates of non-procedural myocardial infarction and repeat revascularisation.
FUNDING
Biosensors.

Identifiants

pubmed: 31879028
pii: S0140-6736(19)32972-1
doi: 10.1016/S0140-6736(19)32972-1
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT01496651']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

191-199

Investigateurs

Niels R Holm (NR)
Timo Mäkikallio (T)
Mitchell Lindsay (M)
Mark S Spence (MS)
Andrejs Erglis (A)
Ian B A Menown (IBA)
Thor Trovik (T)
Markku Eskola (M)
Hannu Romppanen (H)
Tholmas Kellerth (T)
Lisette O Jensen (LO)
Gintaras Kalinauskas (G)
Rikard B A Linder (RBA)
Markku Pentikainen (M)
Anders Hervold (A)
Adrian Banning (A)
Azfar Zaman (A)
James Cotton (J)
Erlend Eriksen (E)
Sulev Margus (S)
Lone J H Mogensen (LJH)
Per H Nielsen (PH)
Matti Niemelä (M)
Kari Kervinen (K)
Jens F Lassen (JF)
Keith Oldroyd (K)
Geoff Berg (G)
Simon J Walsh (SJ)
Colm G Hanratty (CG)
Indulis Kumsars (I)
Peteris Stradins (P)
Terje K Steigen (TK)
Ole Fröbert (O)
Alastair Nj Graham (AN)
Petter C Endresen (PC)
Matthias Corbascio (M)
Olli Kajander (O)
Uday Trivedi (U)
Juha Hartikainen (J)
Ves Anttila (V)
David Hildick-Smith (D)
Leif Thuesen (L)
Evald H Christiansen (EH)

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Niels R Holm (NR)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Timo Mäkikallio (T)

Department of Cardiology, Oulu University Hospital, Oulu, Finland.

M Mitchell Lindsay (MM)

Department of Cardiology, Golden Jubilee National Hospital, Clydebank, UK.

Mark S Spence (MS)

Belfast Heart Centre, Belfast Trust, Belfast, UK.

Andrejs Erglis (A)

Latvia Centre of Cardiology, Paul Stradins Clinical Hospital, Riga, Latvia.

Ian B A Menown (IBA)

Craigavon Cardiac Centre, Craigavon, UK.

Thor Trovik (T)

Department of Cardiology, University Hospital of North Norway, Tromsø, Norway.

Thomas Kellerth (T)

Department of Cardiology, Faculty of Health, Örebro University, Örebro, Sweden.

Gintaras Kalinauskas (G)

Vilnius University, Clinic of Cardiac and Vascular Diseases, Vilnius, Lithuania.

Lone Juul Hune Mogensen (LJH)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Per H Nielsen (PH)

Department of Cardiac Surgery, Aarhus University Hospital, Aarhus, Denmark.

Matti Niemelä (M)

Department of Cardiology, Oulu University Hospital, Oulu, Finland.

Jens F Lassen (JF)

Department of Cardiology, Odense University Hospital, Odense, Denmark.

Keith Oldroyd (K)

Department of Cardiology, Golden Jubilee National Hospital, Clydebank, UK.

Geoffrey Berg (G)

Department of Cardiac Surgery, Golden Jubilee National Hospital, Clydebank, UK.

Peteris Stradins (P)

Latvia Centre of Cardiology, Paul Stradins Clinical Hospital, Riga, Latvia.

Simon J Walsh (SJ)

Belfast Heart Centre, Belfast Trust, Belfast, UK.

Alastair N J Graham (ANJ)

Belfast Heart Centre, Belfast Trust, Belfast, UK.

Petter C Endresen (PC)

Department of Cardiovascular Surgery, University Hospital of North Norway, Tromsø, Norway.

Ole Fröbert (O)

Department of Cardiology, Faculty of Health, Örebro University, Örebro, Sweden.

Uday Trivedi (U)

Sussex Cardiac Centre, Brighton and Sussex University Hospital, Brighton, UK.

Vesa Anttila (V)

Department of Cardiac Surgery, Oulu University Hospital, Oulu, Finland.

David Hildick-Smith (D)

Sussex Cardiac Centre, Brighton and Sussex University Hospital, Brighton, UK.

Leif Thuesen (L)

Department of Cardiology, Aalborg University Hospital, Aalborg, Denmark.

Evald H Christiansen (EH)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark. Electronic address: evald.christiansen@dadlnet.dk.

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