Class: Supportive Care
Generic Name: Denosumab
Trade Name: Xgeva®
How is this drug used? Xgeva is FDA approved for the prevention of skeletal-related events (such as fractures) in patients with bone metastases from solid (not blood-related) cancers. Xgeva is not approved for use in patients with multiple myeloma.
What is the mechanism of action? Xgeva targets a protein known as the RANK ligand. This protein regulates the activity of osteoclasts (cells that break down bone).
How is Xgeva given (administered)? Xgeva is given as a subcutaneous (under-the-skin) injection every four weeks.
How are patients monitored? Patients will usually have scheduled meetings with their healthcare provider while they are being treated with Xgeva. Patients may undergo blood tests, physical examinations, scans or other measures to assess side effects and response to therapy.
What are the common (occur in 30% or more of patients) side effects of treatment with Xgeva?
What are the less common (occur in 10% to 29% of patients) side effects of treatment with Xgeva?
Osteonecrosis of the Jaw
Some bone drugs, including Xgeva, have been linked with a condition known as osteonecrosis of the jaw (ONJ; death of bone in the jaw). In clinical trials, 2.2% of patients receiving Xgeva developed ONJ. Patients should receive an oral examination and appropriate preventive dentistry prior to starting treatment with Xgeva. During treatment with Xgeva, patients should practice proper oral hygiene, receive routine dental care, and avoid invasive dental procedures.
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 unusual symptoms. Notify your healthcare provider immediately if you experience symptoms of hypocalcemia (low calcium levels), such as muscle stiffness, twitching, spasms, or cramps; symptoms of ONJ, such as pain, numbness, swelling, or slow healing of the jaw, mouth, or teeth; or if you become pregnant or begin nursing.
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 © 2011 CancerConnect Last updated 02/11.
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