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- Bone metastasis
Coping and support (2)
- Palliative care: Symptom relief during illness
- Support groups: Make connections, get help
- Genetic testing for breast cancer: Psychological and social impact
- Breast cancer chemoprevention: Medicines that reduce breast cancer risk
- Breast cancer prevention: How to reduce your risk
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- Breast exam
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Breast cancer chemoprevention: Medicines that reduce breast cancer risk
Aromatase inhibitors are commonly used to treat breast cancer that's hormone-receptor positive in postmenopausal women. These drugs aren't widely used for breast cancer chemoprevention, but they may be an option for some women. Aromatase inhibitors are the subject of much ongoing research.
How they work
Aromatase inhibitors are a class of medicines that reduce the amount of estrogen in your body, depriving breast cancer cells of the fuel they need to grow and thrive. Three aromatase inhibitors are currently used in the treatment of postmenopausal women with breast cancer: anastrozole (Arimidex), exemestane (Aromasin) and letrozole (Femara). These medications are used after breast cancer surgery to prevent breast cancer from returning (recurring) in postmenopausal women with estrogen- or progesterone-responsive tumors.
Who it's for
Aromatase inhibitors have been studied and shown to be effective in postmenopausal women to treat breast cancer and to prevent breast cancer recurrence. Aromatase inhibitors are not intended for preventing breast cancer recurrence in women who still have menstrual cycles.
Aromatase inhibitors are being studied to see if they may reduce the risk of breast cancer in high-risk women, such as those with a family history of breast cancer or a history of precancerous breast lesions. Studies have shown promise in these high-risk women. Based on these results, some women and their doctors may choose to use aromatase inhibitors to reduce the risk of breast cancer, though these drugs aren't approved for this use.
Common side effects
Common side effects of aromatase inhibitors include:
- Hot flashes
- Vaginal dryness
- Joint and muscle pain
Aromatase inhibitors raise the risk of:
- Broken bones (fractures)
Because aromatase inhibitors are a newer class of medications, not much is yet known about long-term health risks, such as heart disease. As more results from research studies become available, doctors will have a better idea of the long-term health implications for these drugs and their effectiveness in breast cancer chemoprevention.
Other areas of research
Aspirin and other pain relievers
Several studies have looked into whether common over-the-counter painkillers, such as aspirin, ibuprofen (Advil, Motrin, others) and naproxen sodium (Aleve), may reduce the risk of breast cancer.
Study results are mixed. Some research has found that women who had breast cancer and who regularly take these pain relievers have a slightly decreased risk of breast cancer recurrence. But other studies haven't shown a significant association between breast cancer risk and these pain relievers.
It remains unknown whether aspirin and other pain relievers help protect against breast cancer, and if so, exactly how they do so. Because some pain relievers, such as celecoxib (Celebrex) and naproxen sodium (Aleve), may increase the risk of heart attack and stroke, talk with your doctor to weigh the potential benefits versus the risks of taking these medications in your situation.
Studies are examining whether vitamin D may have some role in preventing breast cancer and breast cancer recurrence. Preliminary research has shown that vitamin D may have anticancer properties. Early studies in breast cancer survivors linked lower than normal vitamin D levels to an increased risk of cancer recurrence. More studies are needed to understand the action and potential benefits of vitamin D.
(2 of 2)
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- American Society of Clinical Oncology clinical practice guideline update on the use of pharmacologic interventions including tamoxifen, raloxifene and aromatase inhibition for breast cancer risk reduction. American Society of Clinical Oncology. http://jco.ascopubs.org/cgi/content/full/27/19/3235. Accessed Dec. 28, 2010.
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