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. 2024 Nov 19:12:100624.
doi: 10.1016/j.apjon.2024.100624. eCollection 2025 Dec.

Frequency of ischemic cardiac events in patients receiving long-term multikinase inhibitor: A report of three cases

Affiliations

Frequency of ischemic cardiac events in patients receiving long-term multikinase inhibitor: A report of three cases

Nao Muraoka et al. Asia Pac J Oncol Nurs. .

Abstract

Objective: To investigate the incidence and characteristics of ischemic cardiac events, specifically major adverse cardiac events (MACE), in patients undergoing long-term treatment with multikinase inhibitors (MKIs) such as lenvatinib and sorafenib.

Methods: A single-center retrospective analysis was conducted on 41 patients treated with lenvatinib or sorafenib for more than one year at our institution from 2015 to 2022. Patient records were reviewed to collect data on demographics, cancer type, cardiovascular risk factors, MKI treatment duration, and MACE incidence. MACE events, defined as acute heart failure, fatal arrhythmia, acute myocardial infarction, and coronary revascularization, were analyzed to determine potential correlations with MKI therapy.

Results: Among the 41 patients, three (7.3%) developed MACE, presenting as acute heart failure, fatal arrhythmia, and acute myocardial infarction, all associated with significant coronary artery stenosis. Notably, none of these patients had a prior history of cardiovascular disease. Despite variations in clinical presentation, all cases suggested a link between long-term MKI administration and accelerated coronary atherosclerosis. Factors involved in atherosclerosis were significantly older and tended to be more hypertensive in the non-MACE group.

Conclusions: Long-term MKI therapy may increase the risk of severe ischemic cardiac events, likely due to accelerated atherosclerosis. Clinicians and oncology nurses should monitor patients closely for early signs of angina, especially in an outpatient setting, to prevent acute cardiac events. Further large-scale studies are warranted to establish a clearer causal relationship between MKI therapy and cardiovascular risks.

Keywords: Atherosclerosis; Cardio-oncology nursing; Cardiotoxicity management; Cardiovascular assessment; MACE; Multikinase inhibitor.

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Conflict of interest statement

Dr. Kenmotsu received research funding from Ono Pharmaceutical Co, Ltd., Novartis Pharma K.K., Eli Lilly K.K, AstraZeneca K.K., Loxo Oncology, and speakers bureau from Amgen inc., AstraZeneca K.K., Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Chugai Pharmaceutical Co, Ltd., Daiichi-Sankyo Co., Ltd., Eli Lilly K.K, Kyowa Hakko Kirin Co., Ltd., Merck, MSD, Novartis Pharma K.K., Ono Pharmaceutical Co, Ltd., Pfizer, Taiho Pharma, Takeda Pharmaceutical Co., Ltd.

Figures

Fig. 1
Fig. 1
Coronary angiography in Case 1. a: Right coronary artery segment 1, 90%; and segment 2, 100% (collaterals from the left coronary artery). b: Left coronary artery segment 5, 75%; segment 6, 99%; high lateral branch, 99%; segment 11, 99%. c: Intravascular ultrasound image in the right coronary artery.
Fig. 2
Fig. 2
a: Coronary angiography in Case 2 are as follows: segment 5–6, 99%; segment 11, 99%; and segment 13, 90%. b: Intravascular ultrasound image in segment 5–6.
Fig. 3
Fig. 3
a: Coronary angiography in Case 3 are as follows: segment 5, 90%; segment 6, 75%; and segment 11, 25%. b: Coronary computed tomography.

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