Miszczyk Marcin, Sajdok Mateusz, Bednarek Jacek, Latusek Tomasz, Wojakowski Wojciech, Tomasik Bartłomiej, Wita Krystian, Jadczyk Tomasz, Kurzelowski Radosław, Drzewiecka Anna, Cybulska Magdalena, Gardas Rafał, Jarosiński Grzegorz, Dolla Łukasz, Grządziel Aleksandra, Zub Kamil, Bekman Adam, Kaminiów Konrad, Kozub Anna, Gołba Krzysztof S, Blamek Sławomir
III(rd) Radiotherapy and Chemotherapy Department, Maria Skłodowska-Curie National Research Institute of Oncology, Gliwice branch, Wybrzeże Armii Krajowej 15 44-102, Gliwice, Poland.
Department of Electrocardiology, Upper-Silesian Heart Center, 7th Medical University of Silesia Hospital, Ziołowa 45/47 40-635, Katowice, Poland.
Radiother Oncol. 2023 Nov;188:109857. doi: 10.1016/j.radonc.2023.109857. Epub 2023 Aug 18.
Despite its increasing popularity, there are limited prospective data on stereotactic arrhythmia radioablation (STAR). In this trial, we assessed the safety and efficacy of STAR in patients with ventricular tachycardia (VT), focusing on early treatment-related grade ≥ 3 adverse events (AE).
This prospective trial was designed for adults with VT recurrence following catheter ablation (CA) despite adequate pharmacotherapy, or contraindications to CA. A single dose of 25 Gy was delivered to the arrhythmia substrate defined on electro-anatomic mapping and cardiac-gated CT. The primary endpoint was safety, defined as two or fewer treatment-related grade ≥ 3 AEs during the first three months in 11 patients. Additional endpoints included treatment efficacy, clinical and biological markers of cardiac injury, and quality of life.
Eleven patients with a median age of 67 years, structural heart disease, and a clinically significant recurrence of VT despite adequate pharmacotherapy and 1-4 previous CAs were enrolled between 2020/09 and 2022/10. Following the treatment, one patient developed a possibly treatment-related grade ≥ 3 AE, a grade 4 heart failure exacerbation at 87 days, which resolved after conservative treatment. There was a total 84.3% reduction in VT burden in 10 evaluable patients; however, VT recurrence was eventually observed in eight, and three patients required additional CAs. Three deaths due to unrelated causes were recorded.
STAR appears to be safe and efficient. It is a promising treatment for selected patients; however, long-term outcomes remain to be evaluated, and controlled trials comparing STAR with standards of care are missing.
尽管立体定向心律失常射频消融术(STAR)越来越受欢迎,但关于该技术的前瞻性数据有限。在本试验中,我们评估了STAR治疗室性心动过速(VT)患者的安全性和有效性,重点关注早期与治疗相关的≥3级不良事件(AE)。
本前瞻性试验针对尽管进行了充分药物治疗但仍有VT复发或存在导管消融(CA)禁忌证的成年患者。对通过电解剖标测和心脏门控CT确定的心律失常基质给予单次25 Gy剂量的照射。主要终点是安全性,定义为11例患者在最初三个月内与治疗相关的≥3级AE不超过2例。其他终点包括治疗效果、心脏损伤的临床和生物学标志物以及生活质量。
2020年9月至2022年10月期间,纳入了11例患者,中位年龄67岁,患有结构性心脏病,尽管进行了充分药物治疗且既往有1 - 4次CA,但仍有临床上显著的VT复发。治疗后,1例患者出现了可能与治疗相关的≥3级AE,即87天时4级心力衰竭加重,经保守治疗后缓解。10例可评估患者的VT负荷总体降低了84.3%;然而,最终有8例患者出现VT复发,3例患者需要再次进行CA。记录到3例因无关原因死亡。
STAR似乎是安全有效的。对于选定的患者来说,它是一种有前景的治疗方法;然而,长期结果仍有待评估,且缺乏将STAR与标准治疗进行比较的对照试验。