Igawa Yusuke, Hamano Hirofumi, Esumi Satoru, Takeda Tatsuaki, Kajizono Makoto, Kikuoka Ryo, Kimura Ikuya, Zamami Yoshito
Department of Clinical Pharmacology and Pharmacy, Okayama University, Okayama, Japan.
Department of Pharmacy, Okayama University Hospital, Okayama, Japan.
Front Pharmacol. 2024 Dec 2;15:1472008. doi: 10.3389/fphar.2024.1472008. eCollection 2024.
Advances in the early detection and treatment of cancer have significantly improved the prognosis of patients with cancer. Tyrosine kinase inhibitors (TKIs) are effective targeted treatments for various malignancies that act by inhibiting kinase activity. Although these drugs share a common mechanism of action, they differ in their targeted kinases, pharmacokinetics, and side effects. TKIs can cause cardiovascular side effects, which adversely affect the prognosis of cancer survivors. This study aimed to assess the risk of cardiac toxicity associated with TKIs using the World Health Organization Global Database, VigiBase.
We conducted a cross-sectional analysis of data from VigiBase, a comprehensive global database of suspected drug reactions. The dataset included reports up to December 2022. We identified patients treated with Food and Drug Administration-approved TKIs and analyzed their age and sex data. The primary outcome was cardiovascular impairment, defined by 21 preferred terms in the Medical Dictionary for Regulatory Activities Terminology version 25.1. Disproportionality analysis using the reported odds ratio was performed to detect adverse cardiovascular signals. Statistical analyses were conducted using R 3.3.2, with a P-value <0.05 considered significant.
Of the 32, 520, 983 reports in VigiBase, 23, 181, 539 were eligible for the analysis. Significant cardiovascular signals were identified for 17 TKIs, including erlotinib, gefitinib, and imatinib. Stratified analyses revealed potential sex- and age-related differences in the risk of adverse events. Heatmaps indicated significant signals for drugs such as lapatinib in males and gefitinib in younger patients.
Our findings indicate that some TKIs, particularly those classified as VEGFR, BCR-ABL, and BTK, pose similar risks of cardiotoxicity, while others, including EGFR, HER2, and ALK TKIs, exhibit varied risk profiles. These results underscore the importance of individualized risk assessment and management of TKI-treated patients. In conclusion, this study provides valuable insights into the cardiotoxic risk of TKIs, which is essential for developing tailored treatment plans.
癌症早期检测和治疗方面的进展显著改善了癌症患者的预后。酪氨酸激酶抑制剂(TKIs)是通过抑制激酶活性对各种恶性肿瘤有效的靶向治疗药物。尽管这些药物具有共同的作用机制,但它们在靶向激酶、药代动力学和副作用方面存在差异。TKIs可引起心血管副作用,这对癌症幸存者的预后产生不利影响。本研究旨在使用世界卫生组织全球数据库VigiBase评估与TKIs相关的心脏毒性风险。
我们对VigiBase(一个全面的全球疑似药物不良反应数据库)的数据进行了横断面分析。数据集包括截至2022年12月的报告。我们确定了接受美国食品药品监督管理局批准的TKIs治疗的患者,并分析了他们的年龄和性别数据。主要结局是心血管损害,由《监管活动医学词典术语》第25.1版中的21个首选术语定义。使用报告比值比进行不成比例分析以检测不良心血管信号。使用R 3.3.2进行统计分析,P值<0.05被认为具有统计学意义。
在VigiBase的32520983份报告中,23181539份符合分析条件。确定了17种TKIs存在显著的心血管信号,包括厄洛替尼、吉非替尼和伊马替尼。分层分析揭示了不良事件风险中潜在的性别和年龄相关差异。热图显示拉帕替尼等药物在男性中以及吉非替尼在年轻患者中存在显著信号。
我们的研究结果表明,一些TKIs,特别是那些归类为VEGFR、BCR-ABL和BTK的药物,具有相似的心脏毒性风险,而其他药物,包括EGFR、HER2和ALK TKIs,则表现出不同的风险特征。这些结果强调了对接受TKIs治疗的患者进行个体化风险评估和管理的重要性。总之,本研究为TKIs的心脏毒性风险提供了有价值的见解,这对于制定个性化治疗方案至关重要。