Phase I/II Trial of Electrophysiology-Guided Noninvasive Cardiac Radioablation for Ventricular Tachycardia

被引:283
作者
Robinson, Clifford G. [1 ]
Samson, Pamela P. [1 ]
Moore, Kaitlin M. S. [2 ]
Hugo, Geoffrey D. [1 ]
Knutson, Nels [1 ]
Mutic, Sasa [1 ]
Goddu, S. Murty [1 ]
Lang, Adam [3 ]
Cooper, Daniel H. [2 ]
Faddis, Mitchell [2 ]
Noheria, Amit [2 ]
Smith, Timothy W. [2 ]
Woodard, Pamela K. [4 ]
Gropler, Robert J. [4 ]
Hallahan, Dennis E. [1 ]
Rudy, Yoram [5 ,6 ,7 ,8 ,9 ]
Cuculich, Phillip S. [2 ]
机构
[1] Washington Univ, Dept Radiat Oncol, St Louis, MO USA
[2] Washington Univ, Dept Internal Med, Cardiovasc Div, St Louis, MO USA
[3] Washington Univ, Dept Pathol, St Louis, MO 63130 USA
[4] Washington Univ, Mallinckrodt Inst Radiol, St Louis, MO USA
[5] Washington Univ, Dept Biomed Engn, St Louis, MO USA
[6] Washington Univ, Dept Cell Biol & Physiol, St Louis, MO USA
[7] Washington Univ, Dept Med, St Louis, MO USA
[8] Washington Univ, Dept Radiol, St Louis, MO USA
[9] Washington Univ, Dept Pediat, St Louis, MO 63130 USA
基金
美国国家卫生研究院;
关键词
noninvasive; stereotactic radiotherapy; ventricular tachycardia; STRUCTURAL HEART-DISEASE; BODY RADIATION-THERAPY; CATHETER ABLATION; SUBSTRATE; MORTALITY;
D O I
10.1161/CIRCULATIONAHA.118.038261
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Case studies have suggested the efficacy of catheter-free, electrophysiology-guided noninvasive cardiac radioablation for ventricular tachycardia (VT) using stereotactic body radiation therapy, although prospective data are lacking. Methods: We conducted a prospective phase I/II trial of noninvasive cardiac radioablation in adults with treatment-refractory episodes of VT or cardiomyopathy related to premature ventricular contractions (PVCs). Arrhythmogenic scar regions were targeted by combining noninvasive anatomic and electric cardiac imaging with a standard stereotactic body radiation therapy workflow followed by delivery of a single fraction of 25 Gy to the target. The primary safety end point was treatment-related serious adverse events in the first 90 days. The primary efficacy end point was any reduction in VT episodes (tracked by indwelling implantable cardioverter defibrillators) or any reduction in PVC burden (as measured by a 24-hour Holter monitor) comparing the 6 months before and after treatment (with a 6-week blanking window after treatment). Health-related quality of life was assessed using the Short Form-36 questionnaire. Results: Nineteen patients were enrolled (17 for VT, 2 for PVC cardiomyopathy). Median noninvasive ablation time was 15.3 minutes (range, 5.4-32.3). In the first 90 days, 2/19 patients (10.5%) developed a treatment-related serious adverse event. The median number of VT episodes was reduced from 119 (range, 4-292) to 3 (range, 0-31; P<0.001). Reduction was observed for both implantable cardioverter defibrillator shocks and antitachycardia pacing. VT episodes or PVC burden were reduced in 17/18 evaluable patients (94%). The frequency of VT episodes or PVC burden was reduced by 75% in 89% of patients. Overall survival was 89% at 6 months and 72% at 12 months. Use of dual antiarrhythmic medications decreased from 59% to 12% (P=0.008). Quality of life improved in 5 of 9 Short Form-36 domains at 6 months. Conclusions: Noninvasive electrophysiology-guided cardiac radioablation is associated with markedly reduced ventricular arrhythmia burden with modest short-term risks, reduction in antiarrhythmic drug use, and improvement in quality of life. Clinical Trial Registration: URL: https://www.clinicaltrials.gov/. Unique identifier: NCT02919618.
引用
收藏
页码:313 / 321
页数:9
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