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    Less Frequent Dosing with Herceptin ® As Effective and More Convenient for Breast Cancer

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    According to results recently published in the Journal of Clinical Oncology, Herceptin ® (trastuzumab) given every 3 weeks appear just as effective as the standard weekly dosing in the treatment of advanced breast cancer. 1

    Breast cancer is responsible for approximately 40,000 deaths annually in the United States alone. Metastatic breast cancer refers to cancer that has spread from the breast to several and/or distant sites in the body, often invading vital organs. Although cure rates for breast cancer that is localized and has not spread from its site of origin are high, cure rates with standard treatment for metastatic breast cancer remain dismal. Treatment for metastatic breast cancer is typically not administered with curative intent, but rather to improve quality of life and/or improve the duration of survival. Taxanes (Taxotere ® or paclitaxel) are among the most active chemotherapy agents used for the treatment of breast cancer.

    A type of breast cancer, referred to as human epithelial receptor 2 (HER2)-positive breast cancer, is characterized by the overexpression of HER2 proteins on the surface of the cancer cells. HER2-positive breast cancer is stimulated to grow through biological mechanisms and tends to be aggressive in nature. Herceptin ® (trastuzumab) is a monoclonal antibody that is specifically targeted against HER2-positive cancers and is approved for the treatment of HER2-positive breast cancer. Monoclonal antibodies are proteins that can be synthesized through laboratory processes to recognize and bind to very specific parts of a cell. This binding action stimulates the immune system to fight the cancer and is also implicated in the direct killing of the cancer cell to which it is bound. Herceptin ®, which is often administered with chemotherapy, but can be used alone, is typically given every week.

    Researchers from Canada recently conducted a clinical trial to evaluate the effectiveness of Herceptin ® given every 3 weeks in the treatment of metastatic breast cancer. This trial involved 32 women with HER2-positive breast cancer; 78% of whom had received prior chemotherapy. Patients were treated with Herceptin ® plus paclitaxel (Taxol ®), a commonly used chemotherapy agent in the treatment of breast cancer. Standard dosing for Taxol ® is once every 3 weeks, so researchers administered both Herceptin ® and Taxol ® just once every 3 weeks. Anti-cancer responses were achieved in nearly 60% of patients, and 22% of patients achieved disease stabilization. This dosing schedule was well tolerated.

    The researchers concluded that Herceptin ® given every 3 weeks appears just as effective as every week in the treatment of metastatic HER2-positive breast cancer. A future clinical trial directly comparing schedules of Herceptin ® given once every 3 weeks to once every week may provide confirmatory evidence that less frequent dosing produces just as effective results. A schedule of once every 3 weeks compared to weekly administration would mean improved quality of life for patients by eliminating two-thirds of the office visits for receiving Herceptin ®, as well as an estimated savings of $10,000.00 per year for every patient in medical costs. 2 Patients with HER2- positive breast cancer may wish to speak with their physician about the risks and benefits of receiving treatment once every 3 weeks with their physician, or the participation in a clinical trial further evaluating this scheduling issue. Two sources of information regarding ongoing clinical trials include the National Cancer Institute ( cancer.gov) and www.cancerconsultants.com. Personalized clinical trial searches on behalf of patients are also performed by cancerconsultants.com.

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