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Cardiovascular Toxicity of Targeted Therapies for Cancer: An Overview of Systematic Reviews
Marina T Van Leeuwen1, Steven Luu1, Howard Gurney2
1Centre for Big Data Research in Health, University of New South Wales, Sydney, New South Wales, Australia.
Background:
Several targeted therapies for cancer have been associated with cardiovascular toxicity. The evidence for this association has not been synthesized systematically nor has the quality of evidence been considered. We synthesized systematic review evidence of cardiovascular toxicity of individual targeted agents.
Methods:
We searched MEDLINE, Embase, and the Cochrane Database of Systematic Reviews for systematic reviews with meta-analyses of cardiovascular outcomes for individual agents published to May 2020. We selected reviews according to prespecified eligibility criteria (International Prospective Register of Systematic Reviews CRD42017080014). We classified evidence of cardiovascular toxicity as sufficient, probable, possible, or indeterminate for specific cardiovascular outcomes based on statistical significance, study quality, and size.
Results:
From 113 systematic reviews, we found at least probable systematic review evidence of cardiovascular toxicity for 18 agents, including high- and all-grade hypertension for bevacizumab, ramucirumab, axitinib, cediranib, pazopanib, sorafenib, sunitinib, vandetanib, aflibercept, abiraterone, and enzalutamide, and all-grade hypertension for nintedanib; high- and all-grade arterial thromboembolism (includes cardiac and/or cerebral events) for bevacizumab and abiraterone, high-grade arterial thromboembolism for trastuzumab, and all-grade arterial thromboembolism for sorafenib and tamoxifen; high- and all-grade venous thromboembolism (VTE) for lenalidomide and thalidomide, high-grade VTE for cetuximab and panitumumab, and all-grade VTE for bevacizumab; high- and all-grade left ventricular ejection fraction decline or congestive heart failure for bevacizumab and trastuzumab, and all-grade left ventricular ejection fraction decline/congestive heart failure for pazopanib and sunitinib; and all-grade corrected QT interval prolongation for vandetanib.
Conclusions:
Our review provides an accessible summary of the cardiovascular toxicity of targeted therapy to assist clinicians and patients when managing cardiovascular health.
Insights
Targeted cancer therapies can cause cardiovascular toxicity. This review synthesizes evidence on the cardiovascular risks of 18 targeted agents, aiding clinical management.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Targeted cancer therapies are increasingly used.
- Cardiovascular toxicity is a known concern with these agents.
- Systematic evidence synthesis and quality assessment are lacking.
Purpose of the Study:
- To systematically review and synthesize evidence on the cardiovascular toxicity of targeted cancer therapies.
- To assess the quality of evidence for these associations.
Main Methods:
- Searched MEDLINE, Embase, and Cochrane Database for systematic reviews with meta-analyses of cardiovascular outcomes.
- Included reviews published up to May 2020.
- Classified evidence of toxicity (sufficient, probable, possible, indeterminate) based on statistical significance, study quality, and size.
Main Results:
- Identified probable evidence of cardiovascular toxicity for 18 targeted agents.
- Common toxicities include hypertension, arterial and venous thromboembolism, and left ventricular ejection fraction decline.
- Specific agents like bevacizumab, abiraterone, and trastuzumab showed significant cardiovascular risks.
Conclusions:
- Provides a synthesized summary of cardiovascular toxicity associated with targeted therapies.
- Aims to assist clinicians and patients in managing cardiovascular health during treatment.
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