Treatment After Surgery
Treatment after surgery for breast cancer can include radiation therapy, chemotherapy, and/or hormone therapy.
Radiation Therapy
Radiation therapy, also known as radiotherapy, uses high-energy x-rays to kill cancer cells or keep them from growing. Often patients who have had breast-conservation therapy such as partial mastectomy (lumpectomy, excision, or quadrantectomy) will be treated with a combination of surgery and radiation therapy for five to six weeks to keep the cancer from returning.
The 2 types of radiation therapy are external radiation therapy, which is delivered outside the body by a machine that sends radiation to the cancer site, and internal radiation therapy, which involves placing a radioactive substance in a needle, seed, wire, or catheter directly into or near the tumor or cancer site. The type and stage of the cancer will determine the way your radiation therapy will be delivered.
Chemotherapy
Chemotherapy includes either systemic or regional chemotherapy. Patients treated with systemic chemotherapy are given an oral or injected medication that attacks cancer cells throughout the body. Regional chemotherapy is delivered directly to the spine, an organ, or body cavity to attack the cancer cells in that area. In both cases, chemotherapy kills cancer cells or stops them from dividing. Like radiation therapy, the type and stage of the cancer will determine how chemotherapy will be delivered.
Hormone Therapy
To be clear, hormone replacement therapy (HRT) and hormone therapy for breast cancer are different. Whereas HRT is used to replace hormones in postmenopausal women, hormone therapy for breast cancer is used to reduce or remove hormones such as estrogen to stop them from making certain cancer cells grow. Estrogen will send signals to hormone receptors to encourage this growth. With less estrogen in the body, hormone receptors receive fewer growth signals and cancer growth can be slowed or stopped. Most estrogen is produced by the ovaries before menopause; however, after menopause, most of the estrogen is made from another hormone known as androgen. Aromatase inhibitors inhibit the aromatase enzyme from turning androgen into estrogen, which lowers the amount of estrogen produced outside of the ovaries. With less estrogen in the bloodstream, there will be less estrogen to reach the estrogen receptors—a process that can slow or stop the growth of cancer cells.
Your doctor can determine whether the cancer cells in your breast have places (receptors) where hormones can attach. Receptor-positive, or hormone-dependent, breast cancer refers to cancer cells that are affected by hormones, and receptor-negative breast cancer refers to cancer cells that are not affected by hormones. If you have receptor-positive breast cancer, your doctor will prescribe treatment to reduce or block hormone production in your body.
Some patients with early stage breast cancer or breast cancer that has spread to other body areas (metastatic breast cancer) are often treated with a combination of hormone therapy and tamoxifen. An oral medication, tamoxifen binds to the estrogen receptors on tumors to reduce the risk of breast cancer in patients at high risk for breast cancer or who have noninvasive (ductal carcinoma in situ) or invasive receptor-positive breast cancer. Tamoxifen therapy can be given for up to five years in women before or after menopause. Women with advanced (metastatic) cancer can continue taking tamoxifen as long as it's working.
Because hormone therapy with tamoxifen or estrogens can increase the risk of endometrial cancer and other serious adverse events, women treated with this approach should immediately report vaginal bleeding that is not related to menstruation and have a pelvic examination each year to check for cancer.
Femara® (letrozole) 2.5 mg tablets are approved for the adjuvant (following surgery) treatment of postmenopausal women with hormone receptor-positive early stage breast cancer.
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Indication Important Safety Information Femara is only indicated in postmenopausal women. You should not take Femara if you are premenopausal. Your doctor should discuss the need for adequate birth control if you have the potential to become pregnant, if you are not sure of your postmenopausal status, or if you recently became postmenopausal. You should not take Femara if you are pregnant as it may cause harm to an unborn child. You should also discuss with your doctor what to do if you are nursing a child. The use of Femara may cause decreases in the density of your bones, increases in bone fractures and osteoporosis. Monitoring of the density of your bones may be required. Some patients taking Femara had an increase in cholesterol. Your doctor may require the monitoring of cholesterol in your blood. Some women reported fatigue, dizziness and drowsiness with Femara. Until you know how it affects you, use caution before driving or operating machinery. Some women had moderate, temporary decreases in white blood cell counts. The medical significance of this is not known. The most serious side effects seen with Femara are bone effects (fractures, decreased bone density and osteoporosis) and increases in cholesterol. Other common side effects seen with Femara include joint pain, nausea, weight decrease, vaginal irritiation, and pain in the extremitites. Other important less commonly reported side effects include blood clots, other cancers, stroke, heart attack and endometrial cancer. Femara is a once-daily, convenient prescription tablet. Your doctor may tell you to take Femara every other day if you have severe liver disease. Always take your medicine exactly as prescribed by your doctor. For full prescribing information, please click here. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call |

