Featured
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Review Article |
Breast cancer therapy-associated cardiovascular disease
Use of radiotherapy or chemotherapy generally increases the survival of women with breast cancer; however, the use of radiotherapy, chemotherapy agents, such as the anthracycline doxorubicin, or anti-HER2 agents, such as trastuzumab, confer an increased risk of adverse cardiovascular events in these patients. In this Review, the authors describe the incidence and management of treatment-induced cardiac disease in women with breast cancer, and highlight strategies that might be used to minimize this risk.
- Timothy M. Zagar
- , Daniela M. Cardinale
- & Lawrence B. Marks
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News & Views |
Risk of heart disease after radiotherapy—cause for concern
Radiotherapy is known to cause heart disease. A recent analysis challenges several long-held tenets, indicating that radiation-induced cardiotoxicity might occur at lower doses, and earlier, than generally believed. We must be mindful of this toxicity and limit cardiac radiation dose as much as possible.
- Timothy M. Zagar
- & Lawrence B. Marks
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Review Article |
Thrombosis and cancer
Venous thromboembolism (VTE) is a potentially life-threatening condition that can be associated with significant morbidity and is linked to cancer by numerous pathophysiological mechanisms. Here, the risk factors, mechanisms, prevention, and optimal treatment of VTE in patients with cancer are discussed.
- Annie Young
- , Oliver Chapman
- & Ajay K. Kakkar
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News & Views |
ADT for prostate cancer: true love or heartbreak?
The addition of hormonal therapy to radiation therapy improves survival in men with unfavorable risk prostate cancer. Yet, men with prostate cancer have higher rates of non-cancer death than the general population and most will die from causes other than their index malignancy. Co-morbid cardiovascular disease is strongly associated with cause of death and this raises the possibility that prostate cancer or its treatment increases cardiovascular disease risk and possibly mortality.
- Jason A. Efstathiou
- , William U. Shipley
- & Matthew R. Smith