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阿那曲唑:晚期乳腺癌治疗手段中的新成员。

Anastrozole: a new addition to the armamentarium against advanced breast cancer.

作者信息

Buzdar A U

机构信息

Department of Breast Medical Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Am J Clin Oncol. 1998 Apr;21(2):161-6. doi: 10.1097/00000421-199804000-00014.

Abstract

Estrogen manipulation represents an effective treatment for advanced breast cancer in postmenopausal women with estrogen-receptor positive disease. The antiestrogen agent, tamoxifen, is the first choice for advanced breast cancer in postmenopausal women due to its efficacy and lack of significant side effects. As with all cancer treatments, however, cancer may recur after initial treatment with tamoxifen, and the limitations of currently available alternative hormonal therapies in terms of tolerability and convenience of administration underscore the need for new agents. Anastrozole is a new, highly selective, nonsteroidal aromatase inhibitor capable of maximal estrogen depletion with fewer side effects than other hormonal therapies. Anastrozole is administered in a convenient, once-daily oral dosing regimen and does not require steroid replacement therapy. In two multicenter clinical trials, anastrozole was as effective as megestrol acetate for the treatment of advanced breast cancer in postmenopausal women who progressed after tamoxifen therapy, based on objective response rates and time to objective progression of disease. In addition, the drug did not produce the weight gain observed with megestrol acetate therapy. Anastrozole is an effective endocrine agent in the treatment of advanced breast cancer in postmenopausal women.

摘要

对于患有雌激素受体阳性疾病的绝经后女性晚期乳腺癌,雌激素调控是一种有效的治疗方法。抗雌激素药物他莫昔芬,因其疗效显著且副作用较小,是绝经后女性晚期乳腺癌的首选药物。然而,与所有癌症治疗方法一样,使用他莫昔芬进行初始治疗后癌症可能会复发,并且目前可用的其他激素疗法在耐受性和给药便利性方面的局限性凸显了对新药物的需求。阿那曲唑是一种新型、高选择性、非甾体类芳香化酶抑制剂,能够最大程度地减少雌激素生成,且副作用比其他激素疗法更少。阿那曲唑采用方便的每日一次口服给药方案,无需进行类固醇替代治疗。在两项多中心临床试验中,基于客观缓解率和疾病客观进展时间,对于在他莫昔芬治疗后病情进展的绝经后女性晚期乳腺癌患者,阿那曲唑治疗效果与醋酸甲地孕酮相当。此外,该药物不会产生醋酸甲地孕酮治疗时出现的体重增加现象。阿那曲唑是治疗绝经后女性晚期乳腺癌的一种有效内分泌药物。

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