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恩曲替尼诱发的Brugada综合征导致一名ROS1融合阳性肺腺癌患者发生室性心动过速。

Entrectinib-Induced Brugada Syndrome Leading to Ventricular Tachycardia in A Patient with ROS1 Fusion-Positive Lung Adenocarcinoma.

作者信息

Ishiguro Nobuo, Mori Takeshi, Kaneshiro Makito, Hasegawa Shin, Tanaka Akimitsu, Ando Miyuki, Kato Kazuo

机构信息

Department of Cardiology, Nagoya Tokushukai General Hospital, Nagoya, Japan.

出版信息

Eur J Case Rep Intern Med. 2025 Apr 2;12(5):005232. doi: 10.12890/2025_005232. eCollection 2025.

Abstract

UNLABELLED

A 65-year-old male presented to the emergency room after experiencing syncope while driving, causing a self-inflicted accident. He had previously been diagnosed with stage IV A (cTXN2M1a) lung adenocarcinoma with C-ROS oncogene 1 (ROS1) fusion gene, wherein entrectinib (a multikinase inhibitor of ROS1, 600 mg orally once daily) was initiated as the first-line chemotherapy 12 days prior. He presented with haemodynamically unstable conditions without fever (blood pressure 89/42 mmHg; heart rate, 180/min). The 12-lead electrocardiogram revealed ventricular tachycardia (VT) with a left bundle branch block and right axis deviation. Synchronised electrical cardioversion terminated the sustained VT, and the post-electrocardiogram exhibited coved-type ST-segment elevation in V1 to V3. An emergency coronary angiography showed no abnormal findings. Coved-type ST-segment elevation in V1 to V3 persisted for two days following cessation of entrectinib; however, electrocardiogram findings gradually normalised, with no recurrence of clinical VT. Catheter ablation for VT was initially planned; however, the consultant pulmonologist considered that entrectinib could induce Brugada syndrome (BrS), resulting in sustained VT. Therefore, the plan was suspended and entrectinib was discontinued. Electrophysiological examination with programmed electrical and pilsicainide infusion for risk stratification failed to induce clinical VT, and the patient was considered at low risk for VT recurrence following entrectinib discontinuation. Accordingly, we opted for close observation. At the one-year follow-up, no ventricular arrhythmias were noted. The relationship between entrectinib and drug-induced BrS remains unclear, with few reported cases. Continuous or frequent electrocardiogram monitoring during hospitalisation post entrectinib initiation may help detect entrectinib-induced BrS.

LEARNING POINTS

The relationship between entrectinib and drug-induced Brugada syndrome remains unclear, and reports of entrectinib-induced Brugada syndrome are rare.We performed risk stratification using electrophysiological examinations in a case of entrectinib-induced Brugada syndrome in a patient with ROS1 fusion-positive lung adenocarcinoma.Our results suggest that continuous electrocardiogram monitoring or frequent electrocardiogram recording at least once a day several days following entrectinib initiation may help detect entrectinib-induced Brugada syndrome irrespective of being in or out of hospital.

摘要

未标注

一名65岁男性在驾车时晕厥,导致自伤事故后被送往急诊室。他之前被诊断为IV A期(cTXN2M1a)肺腺癌伴C-ROS原癌基因1(ROS1)融合基因,12天前开始使用恩曲替尼(一种ROS1多激酶抑制剂,每日口服一次,600mg)作为一线化疗。他出现血流动力学不稳定情况,无发热(血压89/42mmHg;心率180次/分钟)。12导联心电图显示室性心动过速(VT)伴左束支传导阻滞和右轴偏移。同步电复律终止了持续性VT,复律后的心电图显示V1至V3导联呈穹窿型ST段抬高。急诊冠状动脉造影未发现异常。停用恩曲替尼后,V1至V3导联的穹窿型ST段抬高持续了两天;然而,心电图结果逐渐恢复正常,临床VT未复发。最初计划对VT进行导管消融;然而,呼吸内科会诊医生认为恩曲替尼可能诱发Brugada综合征(BrS),导致持续性VT。因此,该计划被暂停,恩曲替尼被停用。通过程序性电刺激和静脉注射吡西卡尼进行风险分层的电生理检查未能诱发临床VT,该患者在停用恩曲替尼后被认为VT复发风险较低。因此,我们选择密切观察。在一年的随访中,未发现室性心律失常。恩曲替尼与药物性BrS之间的关系仍不清楚,报告的病例很少。在开始使用恩曲替尼后的住院期间持续或频繁进行心电图监测可能有助于检测恩曲替尼诱发的BrS。

学习要点

恩曲替尼与药物性Brugada综合征之间的关系仍不清楚,关于恩曲替尼诱发Brugada综合征的报告很少。我们对一名ROS1融合阳性肺腺癌患者因恩曲替尼诱发Brugada综合征的病例进行了电生理检查以进行风险分层。我们的结果表明,在开始使用恩曲替尼后的几天内,无论住院与否,持续进行心电图监测或每天至少进行一次频繁的心电图记录可能有助于检测恩曲替尼诱发的Brugada综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aa0/12061223/1e421de799a0/5232_Fig1.jpg

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