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    Responses in Sequential Hormone Therapies for Breast Cancer

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    According to results presented at the 25th annual San Antonio breast cancer symposium, patients with hormone-positive breast cancer appear to respond to sequential hormone therapy, even if they don?t respond to their initial type of hormone therapy.

    Hormone-positive breast cancer is stimulated to grow when exposed to estrogen and/or progesterone, female hormones that circulate in the body. Hormone therapy reduces or prevents the production of estrogen and/or progesterone in the body or reduces the growth stimulatory effects these hormones impart on the cell. At present, different types of hormone therapy are available to patients with hormone-positive breast cancer. Several clinical trials are ongoing to directly compare the different types of hormone therapy in various stages of breast cancer. However, many of these types of hormone therapies are new in the clinical setting. Thus, the optimal sequencing of hormone therapies has not yet been established, and may be different for each individual based on disease characteristics.

    Researchers from England conducted a clinical study to determine whether 122 patients with advanced breast cancer who had already been treated with initial hormonal therapy consisting of either Nolvadex ® (tamoxifen) or Faslodex ® (fulvestrant) benefited from subsequent hormone therapy. In this follow-up study, patients were given questionnaires regarding their subsequent hormone therapies and responses. In this study, clinical benefit is defined as anti-cancer responses or disease stabilization for a minimum of approximately 6 months.

    Of the patients who achieved a clinical benefit from initial hormone therapy with Faslodex ®, 57% achieved a clinical benefit from subsequent hormone therapy with aromatase inhibitors, Nolvadex ®, or megestrol acetate. Of the patients who achieved a clinical benefit from initial therapy with Nolvadex ®, 61% achieved a clinical benefit from subsequent therapy including aromatase inhibitors, megestrol acetate, and medroxyprogesterone acetate.

    Of the patients who did not respond to initial therapy with Faslodex ®, approximately 43% still achieved a clinical benefit from subsequent hormone therapy consisting of either aromatase inhibitors, Nolvadex ®, megestrol acetate, or medroxyprogesterone acetate. Of the patients who did not respond to initial therapy with Nolvadex ®, 57% achieved a clinical benefit from subsequent hormone therapy consisting of aromatase inhibitors and megestrol acetate.

    The Swiss Group for Clinical Cancer Research also conducted a clinical trial to evaluate the effectiveness of Faslodex ® in women with advanced breast cancer who had stopped responding to or had never responded to both Nolvadex ® and an aromatase inhibitor. Treatment with Faslodex ® resulted in a clinical benefit in 34% of these women.

    These results indicate that patients with breast cancer can be successfully treated with sequential hormone therapies, even if they did not respond to their prior hormone therapy. Patients who have stopped responding to hormone therapy may wish to speak with their physician about the risks and benefits of treatment with subsequent hormone therapy or the participation in a clinical trial further evaluating hormone therapy or 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: Carlson, R. Oncology Times. 2003;Special Edition reporting on the 25th annual San Antonio breast cancer symposium: 10-11.

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