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Chemotherapy-induced Vascular Toxicity - Real-time In vivo Imaging of Vessel Impairment
Published on: January 7, 2015
Cardiovascular Complications of Targeted Therapies for Chronic Myeloid Leukemia
Rongras Damrongwatanasuk1, Michael G Fradley2
1Cardio-Oncology Program, Division of Cardiovascular Medicine, University of South Florida and H. Lee Moffitt Cancer Center & Research Institute, 2 Tampa General Circle, Tampa, FL, 33606, USA.
Opinion Statement:
The development of tyrosine kinase inhibitors (TKIs) dramatically changed the treatment landscape for many different cancers including chronic myeloid leukemia (CML). With the introduction of imatinib, the first TKI developed and approved to effectively treat CML, patient survival has increased dramatically and, in some cases, this fatal cancer can be managed as a chronic disease. Since the approval of imatinib in 2002, four additional TKIs have been developed to treat this disease including the second-generation TKIs nilotinib, dasatinib, and bosutinib and the third-generation TKI ponatinib. Despite their significant impact on the progression of CML, there is increasing recognition of cardiovascular toxicities which can limit their long-term use and impact patient morbidity and mortality. The majority of the cardiotoxicities are associated with the second- and third-generation TKIs, the most concerning of which are vascular events including myocardial infarction, stroke and peripheral arterial disease. In addition, QT prolongation, pleural effusions, and both systemic and pulmonary hypertension are also observed. It is essential for both cardiologists and oncologists to possess knowledge of these issues in order to develop appropriate monitoring and risk mitigation strategies to prevent these toxicities and avoid premature cessation of the drug.
Insights
Tyrosine kinase inhibitors (TKIs) have improved chronic myeloid leukemia (CML) treatment, but newer TKIs carry cardiovascular risks. Awareness and monitoring are crucial for managing these side effects and ensuring continued therapy.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Tyrosine kinase inhibitors (TKIs) have revolutionized chronic myeloid leukemia (CML) treatment, significantly improving patient survival.
- Imatinib, the first TKI, transformed CML management, allowing it to be treated as a chronic condition.
- Subsequent generations of TKIs (nilotinib, dasatinib, bosutinib, ponatinib) offer further treatment options.
Purpose of the Study:
- To highlight the emerging cardiovascular toxicities associated with second- and third-generation TKIs used in CML treatment.
- To emphasize the importance of understanding and managing these cardiotoxicities to prevent adverse patient outcomes.
- To underscore the need for collaboration between cardiologists and oncologists in patient care.
Main Methods:
- Review of clinical data and literature concerning TKI-associated cardiotoxicity in CML patients.
- Analysis of reported cardiovascular events linked to specific TKIs.
- Identification of key cardiotoxicities and risk factors.
Main Results:
- Second- and third-generation TKIs are frequently associated with cardiovascular adverse events.
- Major concerns include vascular events (myocardial infarction, stroke, peripheral arterial disease), QT prolongation, pleural effusions, and hypertension.
- These toxicities can limit long-term TKI use and affect patient morbidity and mortality.
Conclusions:
- Cardiovascular toxicities are a significant consideration in patients receiving advanced TKIs for CML.
- Proactive monitoring and risk mitigation strategies are essential for managing these side effects.
- Multidisciplinary collaboration between oncology and cardiology is vital for optimizing patient care and treatment adherence.
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