Key result
Tyrosine kinase inhibitors are associated with class-specific cardiovascular toxicities including hypertension, AF, and LV dysfunction.
Why the study?
The expanding use of tyrosine kinase inhibitors for hematologic and solid malignancies has revealed a spectrum of cardiovascular toxicities varying across drug classes and agents.
What are the class- and agent-specific cardiovascular toxicities associated with tyrosine kinase inhibitors?
What are the class- and agent-specific cardiovascular toxicities associated with tyrosine kinase inhibitors?
Understanding the specific cardiovascular risks of different tyrosine kinase inhibitors is critical for effective monitoring and management of cardio-oncology patients.
Supports class-specific cardio-oncology surveillance; leaves open precise incidence estimates from prospective trials.
Tyrosine kinase inhibitors (TKIs) have transformed the treatment of a broad range of hematologic and solid malignancies. However, their expanding use has revealed a spectrum of cardiovascular (CV) toxicities, varying in frequency and severity across drug classes and individual agent. This review summarized the CV adverse effects associated with major classes of small-molecule TKIs including Bruton tyrosine kinase (BTK) inhibitors, vascular endothelial growth factor (VEGF) inhibitors, BCR-ABL inhibitors, epidermal growth factor receptor (EGFR) inhibitors, BRAF/MEK inhibitors, and anaplastic lymphoma kinase (ALK) inhibitors. It also highlights strategies for cardiac surveillance in accordance with the latest cardio-oncology guidelines. BTK inhibitors are associated with atrial fibrillation, hypertension, and bleeding, with hypertension representing a class effect. Newer agents show lower incidence rates of atrial fibrillation. VEGF TKIs are linked to hypertension, left ventricular (LV) dysfunction, and arterial thromboembolic events. BCR-ABL TKIs demonstrate more agent-specific toxicities, including pulmonary arterial hypertension with dasatinib, arterial thromboembolic events, and corrected QT interval (QTc) prolongation with nilotinib and ponatinib. Ponatinib shows dose-dependent toxicity. Imatinib and bosutinib have the most favorable CV safety profiles. Osimertinib, a third-generation EGFR inhibitor, is associated with LV dysfunction. BRAF and MEK inhibitors, especially when used in combination, are associated with hypertension, LV dysfunction, and QTc prolongation. Lorlatinib, an ALK inhibitor, exhibits a distinct cardiometabolic profile, including hyperlipidemia, hypertension, and weight gain. Understanding the class and agent-specific CV risks of TKIs is critical for monitoring and managing CV toxicities effectively. Individualized surveillance and early intervention, guided by the current guideline recommendations, are essential to minimizing CV complications, maintaining continuity of TKI therapies, and improving patient outcomes.
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Haoyi Zheng (2025) conducted a review in Hematologic and solid malignancies. Tyrosine kinase inhibitors (TKIs) was evaluated on Cardiovascular toxicities. Tyrosine kinase inhibitors are associated with a spectrum of class- and agent-specific cardiovascular toxicities, including hypertension, atrial fibrillation, and left ventricular dysfunction.
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