Table 1.
Commonly prescribed anticancer agents with summary of respective cardiotoxicity profiles
Class | Commonly Prescribed Agents | Trade Name | Incidence of Cardiotoxicitya (%) (Incidence of Left Ventricular Dysfuntion -%) | Reversibility |
---|---|---|---|---|
Anthracyclines | Doxorubicin Epirubicin | Adriamycin Ellence | Dose dependent; up to 26b | + |
HER-2 targeted therapies | ||||
A. Monoclonal Antibodies | Trastuzumab | Herceptin | 4.5c (up to 30% with asymptomatic cardiomyopathy) | +++ |
B. TKIs | Lapatinib | Tykerb | 1.5–2.2g | Uncertain |
VSP inhibitors | ||||
A. Monoclonal Antibodies | Bevacizumab | Avastin | 2.2h | Uncertain |
B. TKIs | Sorafenib Sunitinib |
Nexavar Sutent |
2.1d 4.1e |
+++ |
Other Tyrosine Kinase Inhibitors (TKIs) | Imatinib | Gleevec | 1.7f | Uncertain |
Abbreviations: HER2, human epidermal growth factor receptor 2; TKI, tyrosine kinase inhibitor; VSP, vascular endothelial growth factor signaling pathway.
Note: Definitions of cardiotoxicity used by sources vary, limiting direct comparisons of incidence between agents. Reversibility indicates the percentage of patients who have cardiomyopathy reversibility after cessation of drug treatment and/or initiation of cardioprotective medications. “+” denotes least likely to reverse and “++++” most reversible. We additionally suggest changing the class grades as follow: anthracyclines “+”, Her-2 receptor targeted therapies “+++” and TKIs under VSP inhibitors (see below for clarification of table 1) “+++”.
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