Key result
This review explores the relationship between anthracycline use and cardiotoxicity in breast cancer, as well as available treatment options based on recent Phase III trials.
Why the study?
What are the available treatment options for managing cardiotoxicity in anthracycline-treated breast cancer patients?
What are the available treatment options for managing cardiotoxicity in anthracycline-treated breast cancer patients?
This review summarizes the evidence for managing cumulative dose-dependent cardiotoxicity in breast cancer patients treated with anthracyclines and trastuzumab.
May guide cardiac surveillance during anthracycline therapy in breast cancer; leaves open optimal sequencing with trastuzumab.
Anthracyclines are among the most active chemotherapeutic agents in cancer treatment. Although infrequent, cumulative dose-dependent cardiotoxicity is nevertheless a significant side effect of this therapy resulting in reduced cardiac reserve or even frank cardiac failure. Although used in several types of malignancy, anthracyclines are most commonly used in breast cancer treatment. Importantly, recent advances have also seen the increasing use of another cardiotoxic agent, the monoclonal antibody trastuzumab, both in the metastatic as well as in the adjuvant breast cancer setting. This review discusses the relationship of cardiotoxicity and anthracycline use, particularly in the breast cancer setting, and explores available treatment options for the anthracycline-treated patients based on evidence from recent Phase III trials.
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Ng et al. (2007) conducted a review in Breast cancer with anthracycline-induced cardiotoxicity. Anthracyclines and cardiotoxicity treatments was evaluated. This review explores the relationship between anthracycline use and cardiotoxicity in breast cancer, as well as available treatment options based on recent Phase III trials.
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