Wilkoff BL, Filippatos G, Leclercq C, Gold MR, Hersi AS, Kusano K, Mullens W, Felker GM, Kantipudi C, El-Chami MF, Essebag V, Pierre B, Philippon F, Perez-Gil F, Chung ES, Sotomonte J, Tung S, Singh B, Bozorgnia B, Goel S, Ebert HH, Varma N, Quan KJ, Salerno F, Gerritse B, van Wel J, Schaber DE, Fagan DH, and Birnie D
Background: Continuous automatic optimisation of cardiac resynchronisation therapy (CRT), stimulating only the left ventricle to fuse with intrinsic right bundle conduction (synchronised left ventricular stimulation), might offer better outcomes than conventional CRT in patients with heart failure, left bundle branch block, and normal atrioventricular conduction. This study aimed to compare clinical outcomes of adaptive CRT versus conventional CRT in patients with heart failure with intact atrioventricular conduction and left bundle branch block., Methods: This global, prospective, randomised controlled trial was done in 227 hospitals in 27 countries across Asia, Australia, Europe, and North America. Eligible patients were aged 18 years or older with class 2-4 heart failure, an ejection fraction of 35% or less, left bundle branch block with QRS duration of 140 ms or more (male patients) or 130 ms or more (female patients), and a baseline PR interval 200 ms or less. Patients were randomly assigned (1:1) via block permutation to adaptive CRT (an algorithm providing synchronised left ventricular stimulation) or conventional biventricular CRT using a device programmer. All patients received device programming but were masked until procedures were completed. Site staff were not masked to group assignment. The primary outcome was a composite of all-cause death or intervention for heart failure decompensation and was assessed in the intention-to-treat population. Safety events were collected and reported in the intention-to-treat population. This study is registered with ClinicalTrials.gov, NCT02205359, and is closed to accrual., Findings: Between Aug 5, 2014, and Jan 31, 2019, of 3797 patients enrolled, 3617 (95·3%) were randomly assigned (1810 to adaptive CRT and 1807 to conventional CRT). The futility boundary was crossed at the third interim analysis on June 23, 2022, when the decision was made to stop the trial early. 1568 (43·4%) of 3617 patients were female and 2049 (56·6%) were male. Median follow-up was 59·0 months (IQR 45-72). A primary outcome event occurred in 430 of 1810 patients (Kaplan-Meier occurrence rate 23·5% [95% CI 21·3-25·5] at 60 months) in the adaptive CRT group and in 470 of 1807 patients (25·7% [23·5-27·8] at 60 months) in the conventional CRT group (hazard ratio 0·89, 95% CI 0·78-1·01; p=0·077). System-related adverse events were reported in 452 (25·0%) of 1810 patients in the adaptive CRT group and 440 (24·3%) of 1807 patients in the conventional CRT group., Interpretation: Compared with conventional CRT, adaptive CRT did not significantly reduce the incidence of all-cause death or intervention for heart failure decompensation in the included population of patients with heart failure, left bundle branch block, and intact AV conduction. Death and heart failure decompensation rates were low with both CRT therapies, suggesting a greater response to CRT occurred in this population than in patients in previous trials., Funding: Medtronic., Competing Interests: Declaration of interests BLW reports participating in physician advisory committees of Medtronic, Abbott, Boston Scientific, Biotronik, and Philips, and receiving honoraria from Medtronic, Abbott, Boston Scientific, Biotronik, Philips, and Cook. GF reports receiving lecture fees, participating in committees of trials sponsored by Bayer, Boehringer Ingelheim, Novartis, Servier, Vifor, Impulse Dynamics, and Medtronic, and receiving research grants from the European Union. CL reports participating in a Medtronic advisory board and receiving honoraria from Medtronic, Biotronik, LivaNova, Boston Scientific, and Abbott. MRG reports being a consultant for Medtronic and Boston Scientific and receiving honoraria from Medtronic, Boston Scientific, and EBR Systems. KK reports receiving speaker's honoraria and research grants from Medtronic Japan and Biotronik Japan. GMF reports receiving research grants from the National Heart, Lung, and Blood Institute, American Heart Association, Amgen, Bayer, Bristol Myers Squibb, Merck, Cytokinetics, and CSL-Behring, acting as a consultant for Novartis, Amgen, Bristol Myers Squibb, Cytokinetics, Cardionomic, Boehringer-Ingelheim, American Regent, Abbott, AstraZeneca, Regeneron, Reprieve, Myovant, Sequana, Windtree Therapuetics, Rocket Pharma, and Whiteswell, and serving on clinical endpoint committees or data safety monitoring boards for Amgen, Merck, Medtronic, EBR Systems, V-Wave, and LivaNova. MFE-C reports consultancy work for Medtronic and Boston Scientific. VE reports receiving support from a Clinical Research Scholar Award from the Fonds de recherche du Québec-Santé (FRQS) and honoraria from Abbott, Boston Scientific, and Medtronic. BP reports consultancy work for Abbott, Biotronik, Boston Scientific, and Microport, and receiving honoraria from Medtronic. FP reports receiving research grants from Medtronic, Boston Scientific, and Abbott. ESC reports consultancy work for Medtronic, Abbott, Intershunt, and Cardionomic, and serving on data safety monitoring boards and clinical events committees for LivaNova, EBR, and Abbott. BB reports consultancy work for Medtronic, Boston Scientific, and Pfizer. HHE reports receiving research grants from Medtronic. NV reports consultancy work for Medtronic, Abbott, Biotronik, Boston Scientific, EP Solutions, Implicity, and Pacemate. JvW, BG, DES, and DHF report being employees of Medtronic. DB reports being a mid-career investigator (supported by the Heart and Stroke Foundation of Ontario and the University of Ottawa Chair in Electrophysiology Research) and receiving research funding from Medtronic, Boston Scientific, Boehringer Ingelheim, Bayer, Biotronik, Pfizer, and Bristol Myers Squibb. All other authors declare no competing interests., (Copyright © 2023 Elsevier Ltd. All rights reserved.)