Herceptin (Trastuzumab) for Breast Cancer Treatment
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Herceptin (Trastuzumab) and Breast Cancer: Patients and Caregivers
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Herceptin (Trastuzumab) and Metastatic Breast Cancer

About Herceptin & Metastatic Breast Cancer | What is Herceptin?

Herceptin® (Trastuzumab) is a treatment for women with breast cancer whose tumors have too much HER2 protein. This type of cancer is known as "HER2-positive", "HER2+", or "HER2 overexpressing". HER2+ tumors tend to grow and spread more quickly than tumors that are not HER2+. This is why it is so important to find out your cancer's HER2 status.

Herceptin has over a decade of clinical experience in over 420,000 people with HER2+ metastatic breast cancer.

  • Clinical experience with Herceptin began in the metastatic setting in 1995

Herceptin is the only FDA-approved biologic therapy for HER2 protein-overexpressing metastatic breast cancer. Herceptin in combination with paclitaxel is indicated for treatment of HER2-overexpressing metastatic breast cancer. Herceptin as a single agent is indicated for treatment of HER2-overexpressing breast cancer in patients who have received one or more chemotherapy regimens for metastatic disease.

Herceptin is not chemotherapy or hormonal therapy. Herceptin is a type of targeted cancer therapy known as a monoclonal antibody (sometimes called targeted biologic therapy). Antibodies are part of the body's normal defense against bacteria, viruses, and abnormal cells, such as cancer cells.

  • Monoclonal antibodies are produced in a laboratory by making multiple copies of a single cell. Monoclonal antibodies are designed to recognize a specific protein on certain cells and signal the body's immune system to destroy the cell.
  • Monoclonal antibodies are generally a more targeted therapy than chemotherapy.

To receive Herceptin, your tumor must be tested and be HER2+. Talk to your doctor to ensure if Herceptin is right for you.

What important safety information should I know about Herceptin?

Herceptin treatment can result in heart problems, including those without symptoms (reduced heart function) and those with symptoms (congestive heart failure). The risk and seriousness of these heart problems were highest in people who received both Herceptin and a certain type of chemotherapy (anthracycline). Your doctor will stop or strongly consider stopping Herceptin if you have a significant drop in your heart function.

You should be monitored for decreased heart function before your first dose of Herceptin, and frequently during the time you are receiving Herceptin and after your last dose of Herceptin. If you must permanently or temporarily stop Herceptin due to heart problems, you should be monitored more frequently.

Some patients have had serious infusion reactions and lung problems; fatal infusion reactions have been reported. In most cases, these reactions occurred during or within 24 hours of receiving Herceptin. Your Herceptin infusion should be temporarily stopped if you have shortness of breath or very low blood pressure. Your doctor will monitor you until these symptoms go away. If you have a severe allergic reaction, swelling, lung problems, inflammation of the lung, or severe shortness of breath, your doctor may need to completely stop your Herceptin treatment.

Worsening of low white blood cell counts associated with chemotherapy has also occurred.

Herceptin can cause low amniotic fluid levels and harm to the fetus when taken by a pregnant woman.

The most common side effects associated with Herceptin were fever, nausea, vomiting, infusion reactions, diarrhea, infections, increased cough, headache, fatigue, shortness of breath, rash, low white and red blood cells, and muscle pain.

Because everyone is different, it is not possible to predict what side effects any one person will have. If you have questions or concerns about side effects, talk to your doctor.

Please see full prescribing information for Boxed WARNINGS and additional important safety information.

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