To print: Select File and then Print from your browser's menu --------------------------------------------------------------------------------------- Title: Femara Effective In Postmenopausal Women With Advanced Breast Cancer URL: http://www.pslgroup.com/dg/58552.htm Doctor's Guide February 5, 1998
EAST HANOVER, NJ -- February 5, 1998 -- Clinical data published in this month's Journal of Clinical Oncology show Novartis Pharmaceuticals Corp.'s Femara(TM) (letrozole tablets, USP) 2.5 mg once-a-day therapy to be an effective treatment of advanced breast cancer in postmenopausal women with disease progression following antiestrogen therapy. The study was an international double-blind trial of 551 advanced breast cancer patients. These patients were randomised to one of three treatment arms: 0.5 mg Femara, 2.5 mg Femara or 160 mg of megestrol acetate (MA). The study showed that 2.5 mg Femara once daily to be effective and generally well-tolerated in postmenopausal women with disease progression following antiestrogen therapy (for example, tamoxifen). "In the advanced disease setting when antiestrogen therapy fails, it is vital to have additional treatment options," said David Parkinson, MD, vice president of clinical research at Novartis Pharmaceuticals. "These data demonstrate that Femara may be an effective option to help shrink tumours or slow the progression of the disease in postmenopausal women for whom antiestrogen therapy has failed." In the study, an objective (complete or partial) response to treatment was demonstrated in approximately 24% of those receiving Femara 2.5 mg and in approximately 16% of those receiving megestrol acetate. The study also showed that the median duration of response had not been reached with Femara 2.5 mg; the median duration of response for megestrol acetate had been reached at 18 months. This trial showed that Femara was generally well tolerated. The most common adverse effects with 2.5 mg Femara were musculoskeletal pain, nausea, headache, arthralgia (joint pain), fatigue, vomiting, and dyspnea (breathing difficulty). Typically in treating breast cancer, hormone therapies such as antiestrogens and aromatase inhibitors may be used to block actions of hormones, such as estrogen, that stimulate the growth of hormone-dependent cancer cells. Antiestrogens, such as tamoxifen, block estrogen from stimulating cancer cells by binding to estrogen receptors in the cancer cells. Rather than blocking estrogen from reaching the estrogen receptor sites in cancer cells, aromatase inhibitors reduce the amount of estrogen circulating in the body. As an aromatase inhibitor Femara binds to the enzyme aromatase and inhibits it from converting a precursor hormone -- androstenedione -- to estrogen in tissues, such as fat, liver and muscle. Women whose disease cannot be controlled by antiestrogen therapy may be switched to other hormone therapies, including aromatase inhibitors. In postmenopausal women, the aromatase pathway is the primary source of estrogen production. According to a recent report, nearly 120,000 U.S. women are living with advanced breast cancer. Of these women, the majority are postmenopausal (over the age of 50). More information on: Novartis Pharmaceuticals Corp. --------------------------------------------------------------------------------------------- Copyright © 1999 P\S\L Consulting Group Inc. All rights reserved. Republication or redistribution of P\S\L content is expressly prohibited without the prior written consent of P\S\L. P\S\L shall not be liable for any errors, omissions or delays in this content or any other content on its sites, newsletters or other publications, nor for any decisions or actions taken in reliance on such content. --------------------------------------------------------------------------------------------- This news story was printed from *Doctor's Guide to the Internet* located at http://www.docguide.com --------------------------------------------------------------------------------------- Return to News Story Page This site is maintained by webmaster@pslgroup.com Please contact us with any comments, problems or bugs. All contents Copyright (c) 1998 P\S\L Consulting Group Inc. All rights reserved.