TY - JOUR
T1 - Percutaneous coronary angioplasty versus coronary artery bypass grafting in treatment of unprotected left main stenosis (NOBLE)
T2 - a prospective, randomised, open-label, non-inferiority trial
AU - for the NOBLE study investigators
AU - Mäkikallio, Timo
AU - Holm, Niels R.
AU - Lindsay, Mitchell
AU - Spence, Mark S.
AU - Erglis, Andrejs
AU - Menown, Ian B.A.
AU - Trovik, Thor
AU - Eskola, Markku
AU - Romppanen, Hannu
AU - Kellerth, Thomas
AU - Ravkilde, Jan
AU - Jensen, Lisette O.
AU - Kalinauskas, Gintaras
AU - Linder, Rikard B.A.
AU - Pentikainen, Markku
AU - Hervold, Anders
AU - Banning, Adrian
AU - Zaman, Azfar
AU - Cotton, Jamen
AU - Eriksen, Erlend
AU - Margus, Sulev
AU - Sørensen, Henrik T.
AU - Nielsen, Per H.
AU - Niemelä, Matti
AU - Kervinen, Kari
AU - Lassen, Jens F.
AU - Maeng, Michael
AU - Oldroyd, Keith
AU - Berg, Geoff
AU - Walsh, Simon J.
AU - Hanratty, Colm G.
AU - Kumsars, Indulis
AU - Stradins, Peteris
AU - Steigen, Terje K.
AU - Fröbert, Ole
AU - Graham, Alastair N.J.
AU - Endresen, Petter C.
AU - Corbascio, Matthias
AU - Kajander, Olli
AU - Trivedi, Uday
AU - Hartikainen, Juha
AU - Anttila, Vesa
AU - Hildick-Smith, David
AU - Thuesen, Leif
AU - Christiansen, Evald H.
N1 - Funding Information:
TM has received grants from Biosensors to the institution during the conduct of the study. NRH received institutional research grants from Biosensors, Abbott, Cordis, Medtronic, Biotronik, Reva Medical, Elixir, and Boston Scientific, and received speaker fees from Boston Scientific, ST Jude Medical, and Terumo. ML received grants from Biosensors during the conduct of the study. MS received personal fees from Edwards Lifesciences, Medtronic, and Boston Scientific, outside the submitted work. AE received personal fees from Biosensors, outside the submitted work. IBAM received grants from Bisosensors during the conduct of the study and other grants from Biosensors and Boston Scientific, outside the submitted work. JR reports grants from Biosensors to his institution, outside the submitted work. LOJ reports grants from Biosensors, Terumo, St Jude Medical, and Biotronik to her institution, and personal fees from Biotronik, outside the submitted work. RBAL reports grants from Biosensors to his institution, outside the submitted work. MP reports grants from Biosensors, during the conduct of the study. AB reports personal fees from Abbott Vascular, Medtronic, and Boston Scientific, outside the submitted work and is partially funded by the NIHR Oxford Biomedical Research Centre. JC reports non-financial support from Biosensors, during the conduct of the study and other from Travel Support Medtronic, outside the submitted work. MN and KK report grants from Biosensors to their institution, during the conduct of the study. JFL reports grants from Boston Scientific, St Jude Medical, Biosensors, Biotronik, and Terumo, outside the submitted work. MM reports grants from Boston Scientific, BioSensors International, and Volcano, outside the submitted work. KO reports grants from Biosensors, during the conduct of the study and personal fees from Biosensors, outside the submitted work. GB reports personal fees from Vascutek Ltd, outside the submitted work. IK reports grants from Biosensors to his institution and personal fees from AstraZeneca, outside the submitted work. JH reports grants from Biosensors to his institution, during the conduct of the study. DH-S reports other support from BioSensors, during the conduct of the study. EHC reports grants from Biosensors to his institution. TT, ME, HR, GK, AH, AZ, EE, SM, HTS, PHN, SJW, CGH, PS, ANJG, PCE, MC, TKS, OK, UT, VA, OF, LT, and TK declare no competing interests.
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2016/12/3
Y1 - 2016/12/3
N2 - Background Coronary artery bypass grafting (CABG) is the standard treatment for revascularisation in patients with left main coronary artery disease, but use of percutaneous coronary intervention (PCI) for this indication is increasing. We aimed to compare PCI and CABG for treatment of left main coronary artery disease. Methods In this prospective, randomised, open-label, non-inferiority trial, patients with left main coronary artery disease were enrolled in 36 centres in northern Europe and randomised 1:1 to treatment with PCI or CABG. Eligible patients had stable angina pectoris, unstable angina pectoris, or non-ST-elevation myocardial infarction. Exclusion criteria were ST-elevation myocardial infarction within 24 h, being considered too high risk for CABG or PCI, or expected survival of less than 1 year. The primary endpoint was major adverse cardiac or cerebrovascular events (MACCE), a composite of all-cause mortality, non-procedural myocardial infarction, any repeat coronary revascularisation, and stroke. Non-inferiority of PCI to CABG required the lower end of the 95% CI not to exceed a hazard ratio (HR) of 1·35 after up to 5 years of follow-up. The intention-to-treat principle was used in the analysis if not specified otherwise. This trial is registered with ClinicalTrials.gov identifier, number NCT01496651. Findings Between Dec 9, 2008, and Jan 21, 2015, 1201 patients were randomly assigned, 598 to PCI and 603 to CABG, and 592 in each group entered analysis by intention to treat. Kaplan-Meier 5 year estimates of MACCE were 29% for PCI (121 events) and 19% for CABG (81 events), HR 1·48 (95% CI 1·11–1·96), exceeding the limit for non-inferiority, and CABG was significantly better than PCI (p=0·0066). As-treated estimates were 28% versus 19% (1·55, 1·18–2·04, p=0·0015). Comparing PCI with CABG, 5 year estimates were 12% versus 9% (1·07, 0·67–1·72, p=0·77) for all-cause mortality, 7% versus 2% (2·88, 1·40–5·90, p=0·0040) for non-procedural myocardial infarction, 16% versus 10% (1·50, 1·04–2·17, p=0·032) for any revascularisation, and 5% versus 2% (2·25, 0·93–5·48, p=0·073) for stroke. Interpretation The findings of this study suggest that CABG might be better than PCI for treatment of left main stem coronary artery disease. Funding Biosensors, Aarhus University Hospital, and participating sites.
AB - Background Coronary artery bypass grafting (CABG) is the standard treatment for revascularisation in patients with left main coronary artery disease, but use of percutaneous coronary intervention (PCI) for this indication is increasing. We aimed to compare PCI and CABG for treatment of left main coronary artery disease. Methods In this prospective, randomised, open-label, non-inferiority trial, patients with left main coronary artery disease were enrolled in 36 centres in northern Europe and randomised 1:1 to treatment with PCI or CABG. Eligible patients had stable angina pectoris, unstable angina pectoris, or non-ST-elevation myocardial infarction. Exclusion criteria were ST-elevation myocardial infarction within 24 h, being considered too high risk for CABG or PCI, or expected survival of less than 1 year. The primary endpoint was major adverse cardiac or cerebrovascular events (MACCE), a composite of all-cause mortality, non-procedural myocardial infarction, any repeat coronary revascularisation, and stroke. Non-inferiority of PCI to CABG required the lower end of the 95% CI not to exceed a hazard ratio (HR) of 1·35 after up to 5 years of follow-up. The intention-to-treat principle was used in the analysis if not specified otherwise. This trial is registered with ClinicalTrials.gov identifier, number NCT01496651. Findings Between Dec 9, 2008, and Jan 21, 2015, 1201 patients were randomly assigned, 598 to PCI and 603 to CABG, and 592 in each group entered analysis by intention to treat. Kaplan-Meier 5 year estimates of MACCE were 29% for PCI (121 events) and 19% for CABG (81 events), HR 1·48 (95% CI 1·11–1·96), exceeding the limit for non-inferiority, and CABG was significantly better than PCI (p=0·0066). As-treated estimates were 28% versus 19% (1·55, 1·18–2·04, p=0·0015). Comparing PCI with CABG, 5 year estimates were 12% versus 9% (1·07, 0·67–1·72, p=0·77) for all-cause mortality, 7% versus 2% (2·88, 1·40–5·90, p=0·0040) for non-procedural myocardial infarction, 16% versus 10% (1·50, 1·04–2·17, p=0·032) for any revascularisation, and 5% versus 2% (2·25, 0·93–5·48, p=0·073) for stroke. Interpretation The findings of this study suggest that CABG might be better than PCI for treatment of left main stem coronary artery disease. Funding Biosensors, Aarhus University Hospital, and participating sites.
UR - http://www.scopus.com/inward/record.url?scp=85003691664&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(16)32052-9
DO - 10.1016/S0140-6736(16)32052-9
M3 - Article
C2 - 27810312
AN - SCOPUS:85003691664
SN - 0140-6736
VL - 388
SP - 2743
EP - 2752
JO - The Lancet
JF - The Lancet
IS - 10061
ER -