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一项随机试验,比较两种剂量的新型选择性芳香化酶抑制剂阿那曲唑(瑞宁得)与醋酸甲地孕酮对绝经后晚期乳腺癌患者的疗效。

A randomised trial comparing two doses of the new selective aromatase inhibitor anastrozole (Arimidex) with megestrol acetate in postmenopausal patients with advanced breast cancer.

作者信息

Jonat W, Howell A, Blomqvist C, Eiermann W, Winblad G, Tyrrell C, Mauriac L, Roche H, Lundgren S, Hellmund R, Azab M

机构信息

University Women's Hospital, Eppendorf, Hamburg, Germany.

出版信息

Eur J Cancer. 1996 Mar;32A(3):404-12. doi: 10.1016/0959-8049(95)00014-3.

Abstract

The aim of this study was to compare the efficacy and tolerability of the new aromatase inhibitor 'ARIMIDEX' (anastrozole) with megestrol acetate in the treatment of advanced breast cancer in postmenopausal women. Anastrozole is a new potent and highly selective non-steroidal aromatase inhibitor. We conducted a prospective randomised trial comparing two doses of anastrozole (1 and 10 mg orally once daily) with megestrol acetate (40 mg orally four times daily) in postmenopausal patients with advanced breast cancer who progressed after prior tamoxifen therapy. All patients were analysed for efficacy as randomised (intention to treat) and for tolerability as per treatment received. Of the 378 patients who entered the study, 135 were randomised to anastrozole 1 mg, 118 to anastrozole 10 mg, and 125 patients to megestrol acetate. After a median follow-up of 192 days, response rate which included complete response, partial response and patients who had disease stabilisation for 6 months or more was 34% for anastrozole 1 mg, 33.9% for anastrozole 10 mg and 32.8% for megestrol acetate. There were no statistically significant differences between either dose of anastrozole and megestrol acetate in terms of objective response rate, time to objective progression of disease or time to treatment failure. The three treatments were generally well tolerated, but more patients on megestrol acetate reported weight gain, oedema and dyspnoea as adverse events while more patients on anastrozole reported gastro-intestinal disorders, usually in the form of mild transient nausea. Patients on anastrozole did not report higher incidences of oestrogen withdrawal symptoms. Anastrozole is an effective and well tolerated treatment for postmenopausal patients with advanced breast cancer. The higher 10 mg dose did not result in additional clinical benefit, but was well tolerated reflecting the good therapeutic margin with anastrozole. Based on this data, anastrozole 1 mg should be the recommended therapeutic dose.

摘要

本研究旨在比较新型芳香化酶抑制剂“瑞宁得”(阿那曲唑)与醋酸甲地孕酮治疗绝经后妇女晚期乳腺癌的疗效和耐受性。阿那曲唑是一种新型强效且高度选择性的非甾体芳香化酶抑制剂。我们进行了一项前瞻性随机试验,比较了两种剂量的阿那曲唑(每日口服1毫克和10毫克)与醋酸甲地孕酮(每日口服40毫克,分4次服用)在接受过他莫昔芬治疗后病情进展的绝经后晚期乳腺癌患者中的疗效。所有患者均按随机分组情况进行疗效分析(意向性治疗),并根据所接受的治疗进行耐受性分析。在进入研究的378例患者中,135例被随机分配至阿那曲唑1毫克组,118例被分配至阿那曲唑10毫克组,125例被分配至醋酸甲地孕酮组。中位随访192天后,包括完全缓解、部分缓解以及疾病稳定6个月或更长时间的缓解率,阿那曲唑1毫克组为34%,阿那曲唑10毫克组为33.9%,醋酸甲地孕酮组为32.8%。在客观缓解率、疾病客观进展时间或治疗失败时间方面,阿那曲唑的两种剂量与醋酸甲地孕酮之间均无统计学显著差异。三种治疗方法总体耐受性良好,但醋酸甲地孕酮组更多患者报告体重增加、水肿和呼吸困难等不良事件,而阿那曲唑组更多患者报告胃肠道疾病,通常表现为轻度短暂性恶心。服用阿那曲唑的患者未报告更高的雌激素撤药症状发生率。阿那曲唑是治疗绝经后晚期乳腺癌患者的一种有效且耐受性良好的药物。较高的10毫克剂量并未带来额外的临床益处,但耐受性良好,这反映了阿那曲唑良好的治疗窗。基于此数据,阿那曲唑1毫克应作为推荐治疗剂量。

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