比较接受布氏酪氨酸激酶抑制剂治疗的患者冠心病的发病率和相关风险因素

IF 4.3 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
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引用次数: 0

摘要

治疗领域ASCVD/特殊人群中的心血管疾病背景布鲁顿酪氨酸激酶抑制剂(BTKi)会增加心脏毒性的风险,包括心房颤动和高血压。方法这是一项回顾性单中心研究,研究对象为2014-2024年服用伊布替尼、阿卡布替尼或扎努布替尼的血液恶性肿瘤患者。研究纳入了符合以下标准的患者:年龄 65 岁、使用 BTKi 28 天、患有 CAD。我们测量了人口统计学特征以及CAD特征,包括诊断方式、阻塞性疾病与非阻塞性疾病、血管再通方法(如有)和药物治疗。分类变量通过卡方检验进行分析,显著性水平为 0.05。平均年龄为 76 岁,19% 为女性。在所选的 BTKi 患者中,CAD 的总体患病率为 7-15%,在患病率(P=0.24)和发病率(P=0.69)方面没有统计学差异。在伊布替尼的亚组分析中,高脂血症与新发 CAD 相关(p=0.04)。只有80%的患者接受了他汀类药物治疗,不同BTKi之间没有显著差异(p=0.59)。与服用阿卡布替尼的患者相比,服用伊布替尼的患者服用阿司匹林的比例较低(32% vs 63%; p=0.02)。在有指征的情况下,既往诊断出患有冠状动脉粥样硬化可能不会限制 BTKi 的使用。由于样本量较小,还需要进一步的研究来证实我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COMPARING THE INCIDENCE AND RISK FACTORS ASSOCIATED WITH CORONARY ARTERY DISEASE IN PATIENTS RECEIVING BRUTON'S TYROSINE KINASE INHIBITORS

Therapeutic Area

ASCVD/CVD in Special Populations

Background

Bruton's tyrosine kinase inhibitors (BTKi) have increased risk of cardiotoxicity including atrial fibrillation and hypertension. However, little data exists on the incidence and risk factors associated with coronary artery disease (CAD) for patients on BTKi.

Methods

This was a retrospective single-center study of patients with hematologic malignancies from 2014-2024 on ibrutinib, acalabrutinib, or zanubrutinib. Patients meeting the following criteria were included: age >65 years, BTKi usage >28 days, and CAD. We measured demographics as well as characteristics of CAD including diagnosis modality, obstructive vs non-obstructive disease, revascularization approach (if any), and medical treatment. Categorical variables were analyzed via chi-squared tests at a significance level of 0.05.

Results

Of 534 screened patients, 69 met inclusion criteria. Average age was 76, and 19% were female. Overall prevalence of CAD ranged from 7-15% among the selected BTKi's, with no statistical difference in the prevalence (p=0.24) or incidence of CAD (p=0.69). In sub-group analysis of ibrutinib, hyperlipidemia was associated with new-onset CAD (p=0.04). Only 80% of patients were receiving a statin, with no significant difference between the different BTKi's (p=0.59). Patients on ibrutinib were less likely to be on aspirin compared to those on acalabrutinib (32% vs 63%; p=0.02).

Conclusions

Patients with CAD and hematologic malignancies receiving BTKi's appear to tolerate these therapies without excess coronary disease. A prior diagnosis of CAD may not limit BTKi use when indicated. Due to the small sample size, further research is needed to confirm our findings.
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来源期刊
American journal of preventive cardiology
American journal of preventive cardiology Cardiology and Cardiovascular Medicine
CiteScore
6.60
自引率
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审稿时长
76 days
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