First-in-human study demonstrates reduction of hard-to-reach ventricular tachycardias

(Press-News.org) Berlin, Germany – 8 April 2024:  A new technology using ultralow temperature cryoablation (ULTC) has eliminated clinical ventricular tachycardia (VT) in 94% of patients. The late-breaking science is presented at EHRA 2024, a scientific congress of the European Society of Cardiology (ESC).1 

VT is a leading cause of sudden death in patients with heart failure and a reduced ejection fraction.2 Approximately 30% of patients with ischaemic and non-ischaemic cardiomyopathies develop ventricular arrhythmias including VT.3 Typical therapies to prevent VT include antiarrhythmic medication, such as amiodarone, and an implantable cardioverter-defibrillator (ICD).4 

Principal investigator Dr. Atul Verma of McGill University Health Centre, Montreal, Canada said: “Amiodarone suppresses VT but cannot eliminate it. In addition, the drug is associated with multiple serious side effects, which can lead to discontinuation in approximately 30-40% of patients.5 ICDs can successfully terminate VT with pacing or shocks, but the shocks are painful and are associated with increased mortality in the long-term. Ablation is an important option to eliminate VT but there have been no significant advancements in this therapy since the development of radiofrequency 15 to 20 years ago.” 

Cryocure-VT was a first-in-human clinical trial evaluating the safety and efficacy of ULTC for the treatment of recurrent monomorphic VTs in patients with ischaemic and non-ischaemic cardiomyopathies. ULTC is a new energy source which produces very deep lesions in ventricular tissue and penetrates scar – essential qualities for successful VT ablation. Current technologies, like radiofrequency, achieve limited tissue depth and cannot penetrate scar tissue.  

“The novelty of this trial is the design of the catheter, which can deliver ULTC (down to -180 C) and produce lesions of different tissue depth depending on the duration of the freeze,” said Dr. Verma. “By estimating tissue depth, either from preprocedural or intraprocedural imaging, the operator can choose which depth is required to treat the VT and deliver the required duration of ULTC. This was the first study to investigate whether the technology could work in patients.” 

Cryocure-VT was a single arm study conducted at nine centres in Belgium, Canada, Czechia, France, Germany, and the Netherlands. The study included 64 patients with a history of VT, an indication for ablation, a history of ischaemic or non-ischaemic cardiomyopathy, and an ICD already implanted or planned for implantation immediately after ablation. The mean age of participants was 67 years and three (4.7%) were women. All patients underwent the ablation procedure using the ULTC catheter and the operator’s choice of electroanatomical mapping system. 

The primary endpoints were acute non-inducibility of clinical VTs at the end of the procedure, freedom from major adverse events at 30 days, freedom from any sustained VT (>30 seconds) at six months, and freedom from ICD intervention at six months. 

The primary acute effectiveness endpoint of non-inducibility of clinical VTs post-procedure occurred in 94% (n=51/54) of patients in whom post-ablation induction was attempted. All VTs were eliminated in 85% (n=46/54) of patients. There were no protocol-defined major adverse events at 30 days. There were four serious adverse events (6%), including one asymptomatic ventricular pseudoaneurysm, one small pericardial effusion which resolved without intervention, one small pericardial effusion which was drained, and one case of haemodynamic instability requiring extracorporeal membrane oxygenation (ECMO) support. One patient died of heart failure 26 weeks after the procedure. 

At six months, 38 patients (60%; n=38/63) remained free of any sustained VT, and 51 patients (81%; n=51/63) remained free of ICD shocks.6 There were no significant differences between ischaemic and non-ischaemic cardiomyopathy patients. 

Dr. Verma said: “ULTC ablation of monomorphic VT was effective and relatively safe in patients with ischaemic and non-ischaemic cardiomyopathies. The success rates for this novel procedure were at least as good, if not better, than prior VT radiofrequency ablation trials. The complication rates were consistent with other VT ablation trials. This technology is promising and may be an important advance for VT ablation by allowing the targeting of deeper mid-myocardial, and even epicardial, substrates. More studies, including randomised trials using this device in patients with monomorphic VT, are needed.” 

 

ENDS 

 

Authors: ESC Press Office  
Tel: +33 (0)489 872 075 

Email: press@escardio.org 

Follow us on X @ESCardioNews  

 

Notes to editor 

Funding: Adagio Medical, California, US developed the technology and funded the trial. 

Disclosures: Dr. Verma has been involved in the development of the catheter and has been an adviser to Adagio Medical. 

 

References and notes 

1The Cryocure-VT trial will be presented during the session ‘Late-Breaking Science: ablation’ which takes place on 8 April 2024 at 13:15 CEST in Room 1. 

2Packer M. What causes sudden death in patients with chronic heart failure and a reduced ejection fraction? Eur Heart J. 2020;41(18):1757-1763. 

3Tan NY, Roger VL, Killian JM, et al. Ventricular arrhythmias among patients with advanced heart failure: A population-based study. J Am Heart Assoc. 2022;11(1):e023377. 

4McDonagh TA, Metra M, Adamo M, et al. 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur Heart J. 2021;42(36):3599-3726. 

5Park HS, Kim YN. Adverse effects of long-term amiodarone therapy. Korean J Intern Med. 2014;29(5): 571-573. 

6One patient withdrew consent for follow-up. 

 

About the European Heart Rhythm Association 

The European Heart Rhythm Association (EHRA) is a branch of the European Society of Cardiology (ESC). Its aim is to improve patients’ quality of life and reduce sudden cardiac death by limiting the impact of heart rhythm disturbances.  

 

About the EHRA Congress     #EHRA2024 

EHRA 2024 is the annual congress of the European Heart Rhythm Association (EHRA) of the European Society of Cardiology (ESC). 

 

About the European Society of Cardiology  

The European Society of Cardiology brings together health care professionals from more than 150 countries, working to advance cardiovascular medicine and help people lead longer, healthier lives. 

 

Information for journalists about registration for EHRA 2024 

EHRA 2024 will be held 7 to 9 April at the CityCube Berlin, Germany, and online. Explore the scientific programme. 

Free registration applies to accredited press. 

Credentials: A valid press card or appropriate letter of assignment with proof of three recent published articles. Read the ESC media and embargo policy. 

The ESC Press Office will verify the documents and confirm by email that your press accreditation is valid. 

The ESC Press Office decision is final regarding all press registration requests. 

END