Key result
Long-term multikinase inhibitor therapy linked to ~7% incidence of MACE in cancer patients.
Why the study?
To investigate the incidence and characteristics of ischemic cardiac events, specifically MACE, in patients undergoing long-term multikinase inhibitor treatment such as lenvatinib and sorafenib.
Does long-term multikinase inhibitor therapy increase the risk of major adverse cardiac events in patients with cancer?
Cohort (n=41)
No
Does long-term multikinase inhibitor therapy increase the risk of major adverse cardiac events in patients with cancer?
This study highlights the potential for accelerated coronary atherosclerosis and severe ischemic events in cancer patients undergoing long-term multikinase inhibitor therapy.
May warrant closer cardiac surveillance with prolonged multikinase inhibitors; leaves open causal confirmation in prospective trials.
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.
No takes yet. Share an insight, caveat, or question.
Muraoka et al. (2024) conducted a cohort in Cancer (thyroid, thymic, hepatocellular carcinoma) (n=41). Multikinase inhibitors (lenvatinib or sorafenib) was evaluated on Major adverse cardiac events (MACE), defined as acute heart failure, fatal arrhythmia, acute myocardial infarction, and coronary revascularization. Long-term multikinase inhibitor therapy was associated with a 7.3% incidence of major adverse cardiac events in patients with cancer treated for over one year.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: