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    Taxotere ®-Based Regimen Active as Initial Therapy in Advanced Breast Cancer

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    According to a recent article published in the journal Cancer, the chemotherapy combination consisting of Taxotere ® (docetaxel), Xeloda ® (capecitabine) and Ellence ® (epirubicin) appears very active as initial therapy in patients with advanced breast cancer.

    Breast cancer is diagnosed in approximately 250,000 women annually in the United States. Although cure rates are high in patients with early-stage breast cancer, once the cancer has spread from its site of origin, cure rates are significantly reduced. Physicians are evaluating novel therapeutic approaches in order to improve survival in patients with advanced breast cancer, including new chemotherapy combinations. Patients with stage III breast cancer typically have one of 3 scenarios: 1) a primary cancer that measures less than 5cm (2 inches) in size and causes axillary lymph nodes to be attached to each other or other structures 2) a primary cancer that is greater than 5cm (2 inches) in size and involves axillary lymph nodes or 3) a primary cancer that is attached to the chest wall or skin. Stage III breast cancers are curable with current multi-modality treatment consisting of surgery, chemotherapy, radiation therapy and hormonal therapy. Patients with stage IV breast cancer have cancer that has spread to one or more distant sites in the body from the affected breast. Physicians often treat patients with stage IV breast cancer to prolong duration of survival and/or improve the quality of life.

    Researchers from Italy recently conducted a clinical trial to evaluate a novel chemotherapy combination consisting of Taxotere ®, Xeloda ® and Ellence ® in patients with previously untreated stage III or stage IV breast cancer. Taxotere ® has demonstrated promising results in patients with breast cancer that has recurred following previous therapies and is presently being evaluated in clinical trials for various cancers. In this trial, 33 patients had stage III breast cancer and received this chemotherapy combination prior to surgery and 34 patients had stage IV breast cancer. Following treatment with Taxotere ®/Xeloda ®/Ellence ®, all patients with stage III breast cancer achieved an anti-cancer response, with 10 patients achieving a complete disappearance of cancer. The anti-cancer response rate was 67% for patients with stage IV cancer, with 12% of those patients achieving a complete disappearance of cancer. Disease stabilization occurred in another 24% of patients with stage IV. The most common severe side effect was low blood cell levels accompanied by a fever (febrile neutropenia) which occurred in 16% of patients.

    These researchers concluded that the chemotherapy combination Taxotere ®/Xeloda ®/Ellence ® appears to be very active as initial treatment of advanced breast cancer. Longer follow-up and clinical trials directly comparing various chemotherapy combinations is necessary to determine survival benefits. A large clinical trial is ongoing to compare Taxotere ®/Xeloda ®/Ellence ® to Taxotere ®/Ellence ® in patients with untreated advanced breast cancer. Patients with advanced breast cancer may wish to speak with their physician regarding the risks and benefits of this chemotherapy combination or the participation in a clinical trial evaluating other novel therapeutic approaches. Two sources of information regarding ongoing clinical trials include the National Cancer Institute ( cancer.gov) and www.eCancerTrials.com. eCancerTrials.com also provides personalized clinical trial searches on behalf of patients.

    Reference: Venturini M, Durando A, Garrone O, et al. Capecitabine in combination with docetaxel and epirubicin in patients with previously untreated, advanced breast carcinoma. Cancer. 2003;97:1174-1180.

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