Nabholtz J M, Buzdar A, Pollak M, Harwin W, Burton G, Mangalik A, Steinberg M, Webster A, von Euler M
Cancer-Cross Institute, Edmonton, Alberta, Canada. jean-marc.nabholtz@bcom
J Clin Oncol. 2000 Nov 15;18(22):3758-67. doi: 10.1200/JCO.2000.18.22.3758.
The efficacy and tolerability of anastrozole (Arimidex; AstraZeneca, Wilmington, DE, and Macclesfield, United Kingdom) and tamoxifen were compared as first-line therapy for advanced breast cancer in 353 postmenopausal women.
The randomized, double-blind, multicenter study was designed to evaluate anastrozole 1 mg once daily relative to tamoxifen 20 mg once daily in patients with hormone receptor-positive tumors or tumors of unknown receptor status who were eligible for endocrine therapy. Primary end points were objective response (OR), defined as complete (CR) or partial (PR) response, time to progression (TTP), and tolerability.
Anastrozole was as effective as tamoxifen in terms of OR (21% v 17% of patients, respectively), with clinical benefit (CR + PR + stabilization > or = 24 weeks) observed in 59% of patients on anastrozole and 46% on tamoxifen (two-sided P =.0098, retrospective analysis). Anastrozole had a significant advantage over tamoxifen in terms of TTP (median TTP of 11.1 and 5.6 months for anastrozole and tamoxifen, respectively; two-sided P =.005). The tamoxifen:anastrozole hazards ratio was 1.44 (lower one-sided 95% confidence limit, 1.16). Both treatments were well tolerated. However, thromboembolic events and vaginal bleeding were reported in fewer patients who received anastrozole compared with those who received tamoxifen (4.1% v 8.2% [thromboembolic events] and 1.2% v 3.8% [vaginal bleeding], respectively).
Anastrozole satisfied the predefined criteria for equivalence to tamoxifen. Furthermore, we observed both a significant increase in TTP and a lower incidence of thromboembolic events and vaginal bleeding with anastrozole. These findings indicate that anastrozole should be considered as first-line therapy for postmenopausal women with advanced breast cancer.
比较阿那曲唑(瑞宁得;阿斯利康公司,美国特拉华州威尔明顿市及英国麦克尔斯菲尔德市)与他莫昔芬作为353例绝经后晚期乳腺癌一线治疗药物的疗效和耐受性。
本随机、双盲、多中心研究旨在评估对于适合内分泌治疗的激素受体阳性肿瘤或受体状态不明肿瘤患者,每日一次口服1毫克阿那曲唑与每日一次口服20毫克他莫昔芬的疗效。主要终点为客观缓解率(OR),定义为完全缓解(CR)或部分缓解(PR);疾病进展时间(TTP);以及耐受性。
就客观缓解率而言,阿那曲唑与他莫昔芬疗效相当(分别为21%和17%的患者),接受阿那曲唑治疗的患者中有59%出现临床获益(完全缓解+部分缓解+病情稳定≥24周),接受他莫昔芬治疗的患者中这一比例为46%(双侧P = 0.0098,回顾性分析)。在疾病进展时间方面,阿那曲唑显著优于他莫昔芬(阿那曲唑和他莫昔芬的中位疾病进展时间分别为11.1个月和5.6个月;双侧P = 0.005)。他莫昔芬与阿那曲唑的风险比为1.44(单侧95%置信下限为1.16)。两种治疗的耐受性均良好。然而,与接受他莫昔芬治疗的患者相比,接受阿那曲唑治疗的患者发生血栓栓塞事件和阴道出血的人数较少(分别为4.1%对8.2%[血栓栓塞事件]以及1.2%对3.8%[阴道出血])。
阿那曲唑符合与他莫昔芬等效性的预设标准。此外,我们观察到阿那曲唑不仅使疾病进展时间显著延长,而且血栓栓塞事件和阴道出血的发生率更低。这些发现表明,阿那曲唑应被视为绝经后晚期乳腺癌女性的一线治疗药物。