Class: Biological Therapy
Generic Name: Pertuzumab
Trade Name: Perjeta™
How is this drug used? Perjeta is used for the treatment of HER2-positive, metastatic breast cancer. It is given in combination with Herceptin® (trastuzumab) and Taxotere® (docetaxel), and is intended for people who have not previously been treated with chemotherapy or HER2-targeted therapy for metastatic breast cancer.
What is the mechanism of action? Perjeta targets a protein that is involved in the growth of some breast cancers: the human epidermal growth factor receptor 2 (HER2).
How is Perjeta given (administered)? Perjeta is given as an intravenous (into a vein) infusion.
How are patients monitored? Patients will usually have scheduled meetings with their healthcare provider while they are being treated with Perjeta. Typically, blood will be drawn to check levels of blood cells and to monitor functions of some organ systems. Patients may also undergo physical examinations, scans or other measures to assess side effects and response to therapy.
What are the most common side effects of treatment with Perjeta when Perjeta is used in combination with Herceptin and Taxotere?
What are some of the other, potentially serious side effects of Perjeta?
This is not a complete list of side effects. Some patients may experience other side effects that are not listed here. Patients may wish to discuss with their physician the other less common side effects of this drug, some of which may be serious.
Some side effects may require medical attention. Other side effects do not require medical attention and may go away during treatment. Patients should check with their physician about any side effects that continue or are bothersome.
What can patients do to help alleviate or prevent discomfort and side effects?
Are there any special precautions patients should be aware of before starting treatment?
When should patients notify their physician?
Tell your doctor if you experience any side effects that bother you or don’t go away. Also tell your doctor if you become pregnant during treatment.
What is a package insert?
A package insert is required by the FDA and contains a summary of the essential scientific information needed for the safe and effective use of the drug for healthcare providers and consumers. A package insert typically includes information regarding specific indications, administration schedules, dosing, side effects, contraindications, results from some clinical trials, chemical structure, pharmacokinetics and metabolism of the specific drug. By carefully reviewing the package insert, you will get the most complete and current information about how to safely use this drug. If you do not have the package insert for the drug you are using, your pharmacist or physician may be able to provide you with a copy.
Copyright © 2012 CancerConnect Last updated 06/12.
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