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本文引用的文献

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2
Defining cardiovascular toxicities of cancer therapies: an International Cardio-Oncology Society (IC-OS) consensus statement.定义癌症治疗的心血管毒性:国际心脏肿瘤学会(IC-OS)共识声明。
Eur Heart J. 2022 Jan 31;43(4):280-299. doi: 10.1093/eurheartj/ehab674.
3
Clinical Approach to Cardiovascular Toxicity of Oral Antineoplastic Agents: JACC State-of-the-Art Review.口服抗肿瘤药物心血管毒性的临床处理方法:美国心脏病学会的现状评估。
J Am Coll Cardiol. 2021 Jun 1;77(21):2693-2716. doi: 10.1016/j.jacc.2021.04.009.
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Development and validation of a tool to assess the risk of QT drug-drug interactions in clinical practice.开发和验证一种工具,以评估临床实践中 QT 药物相互作用的风险。
BMC Med Inform Decis Mak. 2020 Jul 23;20(1):171. doi: 10.1186/s12911-020-01181-3.
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接受口服靶向抗肿瘤药物治疗的患者的QTc延长风险:一项基于社区肿瘤学的真实世界分析。

QTc prolongation risk among patients receiving oral targeted antineoplastic medications: A real-world community-based oncology analysis.

作者信息

Reeves David J, Russell Molly, Rao Vijay U

机构信息

Department of Pharmacy Practice, College of Pharmacy and Health Sciences Butler University, Indianapolis, IN, United States.

Franciscan Physician Network, Franciscan Health, Indianapolis, IN, United States.

出版信息

Front Oncol. 2023 Mar 10;13:1098333. doi: 10.3389/fonc.2023.1098333. eCollection 2023.

DOI:10.3389/fonc.2023.1098333
PMID:36969042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10036778/
Abstract

INTRODUCTION

Thirty oral targeted antineoplastic agents are associated with prolongation of the QT interval. However, limited data exists regarding QTc prolongation and associated risk factors in the ambulatory oncology setting.

METHODS

This retrospective study was completed to describe QTc prolongation incidence among patients receiving oral targeted tyrosine kinase inhibitors (TKI) and identify potential risk factors in the ambulatory community-based oncology clinic.

RESULTS

Of the 341 patients identified as receiving oral TKI, 49 with a baseline and follow-up ECG were included. The incidence of QTc prolongation (QTc > 470 ms in males, QTc > 480 ms in females, or >20 ms increase in QTc from baseline) was 24%. Three patients developed significant QTc prolongation (QTc >500 ms or >60 ms increase in QTc from baseline). No patients discontinued therapy primarily due to QTc prolongation or experienced symptomatic torsades de pointes. Analysis of risk factors demonstrated that patients with QTc prolongation were more likely to receive concomitant therapy with a loop diuretic (41% vs 11%, respectively, p=0.029).

DISCUSSION

The frequency of QTc prolongation may be higher in the real-world setting than that observed in clinical trials; however, continuation of therapy may be possible. Patients receiving concomitant loop diuretics should be monitored more closely for QTc prolongation and electrolyte abnormalities.

摘要

引言

三十种口服靶向抗肿瘤药物与QT间期延长有关。然而,关于门诊肿瘤患者中QTc延长及其相关危险因素的数据有限。

方法

本回顾性研究旨在描述接受口服靶向酪氨酸激酶抑制剂(TKI)的患者中QTc延长的发生率,并确定基于社区的门诊肿瘤诊所中的潜在危险因素。

结果

在341名确定接受口服TKI的患者中,49名有基线和随访心电图的患者被纳入研究。QTc延长的发生率(男性QTc>470毫秒,女性QTc>480毫秒,或QTc较基线增加>20毫秒)为24%。三名患者出现显著的QTc延长(QTc>500毫秒或QTc较基线增加>60毫秒)。没有患者主要因QTc延长而停药,也没有患者出现有症状的尖端扭转型室速。危险因素分析表明,QTc延长的患者更有可能同时接受袢利尿剂治疗(分别为41%和11%,p=0.029)。

讨论

在现实环境中,QTc延长的频率可能高于临床试验中观察到的频率;然而,治疗仍可能继续。接受袢利尿剂联合治疗的患者应更密切地监测QTc延长和电解质异常情况。