Department of Radiation Oncology (C.G.R., P.P.S., G.D.H., N.K., S.M., S.M.G., D.E.H.), Washington University, St Louis, MO.
Department of Internal Medicine, Cardiovascular Division (K.M.S.M., D.H.C., M.F., A.N., T.W.S., P.S.C.), Washington University, St Louis, MO.
Circulation. 2019 Jan 15;139(3):313-321. doi: 10.1161/CIRCULATIONAHA.118.038261.
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.
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.
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.
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.
URL: https://www.clinicaltrials.gov/ . Unique identifier: NCT02919618.
病例研究表明,使用立体定向体部放射治疗(Stereotactic Body Radiation Therapy,SBRT)对室性心动过速(Ventricular Tachycardia,VT)进行无导管、基于电生理引导的非侵入性心脏放射消融术具有疗效,尽管缺乏前瞻性数据。
我们对 19 名患有难治性 VT 发作或与室性早搏(Premature Ventricular Contractions,PVCs)相关的心肌病的成年患者进行了一项前瞻性 I/II 期非侵入性心脏放射消融术的试验。心律失常性瘢痕区域通过将无创解剖和电心脏成像与标准 SBRT 工作流程相结合来靶向,然后对目标区域给予单次 25Gy 的剂量。主要安全性终点为治疗后 90 天内的治疗相关严重不良事件。主要疗效终点为治疗前后(治疗后 6 周空白期)任何 VT 发作次数的减少(通过植入式心律转复除颤器进行监测)或任何 PVC 负担的减少(通过 24 小时动态心电图监测仪测量)。使用健康相关的 36 项简表(Short Form-36,SF-36)评估健康相关的生活质量。
19 名患者入选(17 名 VT,2 名 PVC 心肌病)。中位无创消融时间为 15.3 分钟(范围:5.4-32.3)。在治疗后 90 天内,2/19 名患者(10.5%)发生了与治疗相关的严重不良事件。VT 发作次数从 119 次(范围:4-292 次)减少至 3 次(范围:0-31 次;P<0.001)。植入式心律转复除颤器电击和抗心动过速起搏均观察到减少。18 名可评估患者中有 17 名(94%)VT 发作或 PVC 负担减少。89%的患者中有 75%减少了 VT 发作或 PVC 负担。6 个月时总生存率为 89%,12 个月时为 72%。使用双抗心律失常药物的频率从 59%降至 12%(P=0.008)。在 6 个月时,SF-36 量表的 5 个领域中有 5 个的生活质量得到改善。
无导管电生理引导的心脏放射消融术与 VT 负荷明显降低、抗心律失常药物使用减少和生活质量改善相关,但其短期风险适中。
网址:https://www.clinicaltrials.gov/ 。独特标识符:NCT02919618。