Cardiac Substructure Radiation Dose and Associations With Tachyarrhythmia and Bradyarrhythmia After Lung Cancer Radiotherapy

IF 12 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Jacc: Cardiooncology Pub Date : 2024-08-01 DOI:10.1016/j.jaccao.2024.07.005
Katelyn M. Atkins MD, PhD , Samuel C. Zhang MD , Christopher Kehayias PhD , Christian Guthier PhD , John He BA , Jordan O. Gasho BS , Mina Bakhtiar MD , Katrina D. Silos BA , David E. Kozono MD, PhD , Paul C. Zei MD , Anju Nohria MD , Andriana P. Nikolova MD, PhD , Raymond H. Mak MD
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引用次数: 0

Abstract

Background

Arrhythmias are common following radiotherapy for non–small cell lung cancer.

Objectives

The aim of this study was to analyze the association of distinct arrhythmia classes with cardiac substructure radiotherapy dose.

Methods

A retrospective analysis was conducted of 748 patients with locally advanced non–small cell lung cancer treated with radiotherapy. Cardiac substructure dose parameters were calculated. Receiver-operating characteristic curve analyses for predictors of Common Terminology Criteria for Adverse Events grade ≥3 atrial fibrillation (AF), atrial flutter, non-AF and non–atrial flutter supraventricular tachyarrhythmia (SVT), bradyarrhythmia, and ventricular tachyarrhythmia (VT) or asystole were calculated. Fine-Gray regression models were performed (with noncardiac death as a competing risk).

Results

Of 748 patients, 128 (17.1%) experienced at least 1 grade ≥3 arrhythmia, with a median time to first arrhythmia of 2.0 years (Q1-Q3: 0.9-4.2 years). The 2-year cumulative incidences of each arrhythmia group were 8.0% for AF, 2.7% for atrial flutter, 1.8% for other SVT, 1.4% for bradyarrhythmia, and 1.1% for VT or asystole. Adjusting for baseline cardiovascular risk, pulmonary vein (PV) volume receiving 5 Gy was associated with AF (subdistribution HR [sHR]: 1.04/mL; 95% CI: 1.01-1.08; P = 0.016), left circumflex coronary artery volume receiving 35 Gy with atrial flutter (sHR: 1.10/mL; 95% CI: 1.01-1.19; P = 0.028), PV volume receiving 55 Gy with SVT (sHR: 1.03 per 1%; 95% CI: 1.02-1.05; P < 0.001), right coronary artery volume receiving 25 Gy with bradyarrhythmia (sHR: 1.14/mL; 95% CI: 1.00-1.30; P = 0.042), and left main coronary artery volume receiving 5 Gy with VT or asystole (sHR: 2.45/mL; 95% CI: 1.21-4.97; P = 0.013).

Conclusions

This study revealed pathophysiologically distinct arrhythmia classes associated with radiotherapy dose to discrete cardiac substructures, including PV dose with AF and SVT, left circumflex coronary artery dose with atrial flutter, right coronary artery dose with bradyarrhythmia, and left main coronary artery dose with VT or asystole, guiding potential risk mitigation approaches.

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肺癌放疗后心脏结构的辐射剂量及其与快速性心律失常和缓慢性心律失常的关系
背景 非小细胞肺癌放疗后常见心律失常。计算了心脏亚结构剂量参数。计算了不良事件通用术语标准≥3级心房颤动(AF)、心房扑动、非AF和非心房扑动室上性心动过速(SVT)、缓慢性心律失常、室性心动过速(VT)或间歇的预测因素的受体工作特征曲线分析。结果 748 例患者中,128 例(17.1%)至少出现过 1 次≥3 级心律失常,首次心律失常的中位时间为 2.0 年(Q1-Q3:0.9-4.2 年)。每组心律失常的 2 年累计发病率分别为:房颤 8.0%、心房扑动 2.7%、其他 SVT 1.8%、缓慢性心律失常 1.4%、VT 或心搏过速 1.1%。调整基线心血管风险后,肺静脉(PV)容积接受 5 Gy 与房颤相关(亚分布 HR [sHR]:1.04/mL;95% CI:1.01-1.08;P = 0.016),左侧冠状动脉周容积接受 35 Gy 与心房扑动相关(sHR:1.10/mL;95% CI:1.01-1.19;P = 0.028)、接受 55 Gy 的 PV 容量伴 SVT(sHR:1.03/1%;95% CI:1.02-1.05;P <;0.001)、接受 25 Gy 的右冠状动脉容量伴缓慢性心律失常(sHR:1.14/mL;95% CI:1.00-1.30;P = 0.042),左冠状动脉主干容积接受 5 Gy 后出现 VT 或心搏骤停(sHR:2.45/mL;95% CI:1.21-4.97;P = 0.013)。结论这项研究揭示了病理生理学上不同的心律失常等级与心脏离散亚结构的放疗剂量相关,包括房颤和室上性心动过速的外周血管剂量、心房扑动的左冠状动脉环流剂量、缓慢性心律失常的右冠状动脉剂量以及VT或心搏过速的左主冠状动脉剂量,为潜在的风险缓解方法提供了指导。
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来源期刊
CiteScore
12.50
自引率
6.30%
发文量
106
期刊介绍: JACC: CardioOncology is a specialized journal that belongs to the esteemed Journal of the American College of Cardiology (JACC) family. Its purpose is to enhance cardiovascular care for cancer patients by publishing high-quality, innovative scientific research and sharing evidence-based knowledge. The journal aims to revolutionize the field of cardio-oncology and actively involve and educate professionals in both cardiovascular and oncology fields. It covers a wide range of topics including pre-clinical, translational, and clinical research, as well as best practices in cardio-oncology. Key areas of focus include understanding disease mechanisms, utilizing in vitro and in vivo models, exploring novel and traditional therapeutics (across Phase I-IV trials), studying epidemiology, employing precision medicine, and investigating primary and secondary prevention. Amyloidosis, cardiovascular risk factors, heart failure, and vascular disease are some examples of the disease states that are of particular interest to the journal. However, it welcomes research on other relevant conditions as well.
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