Treatment After Surgery

Treatment After Surgery

Treatment after surgery for breast cancer can include radiation therapy, chemotherapy, and/or hormone therapy.

Adjuvant Systemic 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 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 tablets) is approved for the adjuvant (following surgery) treatment of postmenopausal women with hormone receptor-positive  early stage breast cancer. The benefits of Femara in clinical trials are based on 24 months of treatment. Further follow-up will be needed to determine long-term results, safety and efficacy.


Learn more about Femara patient programs Learn more about Femara patient programs

*The Femara Cares Program™ Prescription Discount Card allows you to pay only $10 for your Femara prescriptions, if you are eligible. Novartis Pharmaceuticals Corporation will pay the rest, up to a maximum of $800 in any 12-month period, toward your Femara prescriptions. This card is subject to change or termination at any time.

Not all patients will receive a total of $800 per year off their prescriptions. Total value of card determined by applicable patient co-pay or out-of-pocket cost.

The Femara Cares Program™ Prescription Discount Card is not valid for prescriptions for which payment may be made in whole or in part under federal or state healthcare programs, including but not limited to, Medicare or Medicaid, or for residents in MA. Limitations apply.

 

Indication
Femara® (letrozole tablets) is approved for the adjuvant (following surgery) treatment of postmenopausal women with hormone receptor-positive early stage breast cancer. The benefits of Femara in clinical trials are based on 24 months of treatment. Further follow-up will be needed to determine long-term results, safety and efficacy.

Femara is also approved for the extended adjuvant treatment of early stage breast cancer in postmenopausal women who are within three months of completion of five years of tamoxifen therapy. The benefits of Femara in clinical trials are based on 24 months of treatment. Further follow-up will be needed to determine long-term results, including side effects.

In addition, Femara is approved for the treatment of postmenopausal women with estrogen receptor-positive or estrogen receptor-unknown breast cancer that has spread to another part of the body (metastatic cancer). Femara is also indicated for the treatment of advanced breast cancer in postmenopausal women with disease progression following antiestrogen therapy.

Important Safety Information

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. Femara is only indicated in postmenopausal women. Talk to your doctor if you're allergic to Femara or any of its ingredients. You should not take Femara if you are pregnant as it may cause harm to an unborn child. Some women reported fatigue and dizziness with Femara. Until you know how it affects you, use caution before driving or operating machinery. Some patients taking Femara had an increase in cholesterol. Additional follow-up is needed to determine the risk of bone fracture associated with long-term use of Femara.

In the adjuvant setting, commonly reported side effects are generally mild to moderate. The most common side effects seen with Femara include hot flashes, joint pain, night sweats, weight gain, nausea, tiredness, other heart-related events, and bone fractures. Other less commonly reported side effects include vaginal bleeding, blood clots, other cancers, osteoporosis, stroke, heart attack, and endometrial cancer.

In the extended adjuvant setting, commonly reported side effects are generally mild to moderate. Commonly reported side effects for Femara include hot flashes, fatigue, joint pain, headache, increase in sweating, swelling due to fluid retention, increase in cholesterol, dizziness, constipation, nausea, heart-related problems, muscle pain, osteoporosis, arthritis, and bone fracture.

In the metastatic cancer setting, commonly reported side effects are generally mild to moderate and may include bone pain, hot flashes, back pain, nausea, joint pain, shortness of breath, tiredness, coughing, constipation, limb pain, chest pain, and headache.

Femara is a once-daily convenient prescription tablet.

For additional safety information, please see the prescribing information.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call
1-800-FDA-1088.