Kaufmann Manfred, Jonat Walter, Hilfrich Jörn, Eidtmann Holger, Gademann Günther, Zuna Ivan, von Minckwitz Gunter
Department of Obstetrics and Gynaecology, J.W. Goethe-University of Frankfurt, Frankfurt am Main, Frankfurt/Main, Germany.
J Clin Oncol. 2007 Jul 1;25(19):2664-70. doi: 10.1200/JCO.2006.08.8054. Epub 2007 Jun 11.
In postmenopausal women with estrogen receptor-positive early breast cancer, surgery is usually followed by a 5-year course of tamoxifen. This report presents results of a prospective, open-label, randomized study, designed to evaluate the benefits of switching to anastrozole after 2 years of tamoxifen treatment, compared with continuing on tamoxifen for 5 years.
After receiving tamoxifen treatment for 2 years, eligible patients (n = 979) were randomly assigned to switch to anastrozole (1 mg/d) or continue tamoxifen (20 or 30 mg/d) for an additional 3 years. Patients were monitored every 6 months during years 1 to 3 and annually thereafter. The primary efficacy variable was disease-free survival, including local or distant recurrence, new contralateral breast cancer, or death. Secondary variables were overall survival and assessment of safety.
Switching to anastrozole resulted in a significant reduction in the risk of disease recurrence (hazard ratio [HR], 0.66; 95% CI, 0.44 to 1.00; P = .049), and improved overall survival (HR, 0.53; 95% CI, 0.28 to 0.99; P = .045) compared with continuing on tamoxifen. Fewer patients who switched to anastrozole reported serious adverse events (22.7% v 30.8%) compared with those who continued on tamoxifen, mainly due to more patients in the tamoxifen group with endometrial events. The overall safety profile for anastrozole was consistent with previous reports and no new safety issues were identified.
Postmenopausal women who have taken tamoxifen for 2 years as adjuvant therapy are less likely to experience a recurrence of breast cancer and have improved overall survival if they switch to anastrozole compared with continuing to receive tamoxifen.
在雌激素受体阳性的绝经后早期乳腺癌女性患者中,手术通常之后会进行5年的他莫昔芬治疗。本报告展示了一项前瞻性、开放标签、随机研究的结果,该研究旨在评估他莫昔芬治疗2年后换用阿那曲唑的益处,并与继续使用他莫昔芬5年进行比较。
在接受他莫昔芬治疗2年后,符合条件的患者(n = 979)被随机分配换用阿那曲唑(1毫克/天)或继续使用他莫昔芬(20或30毫克/天)再治疗3年。在第1至3年期间,每6个月对患者进行监测,此后每年监测一次。主要疗效变量为无病生存期,包括局部或远处复发、新发对侧乳腺癌或死亡。次要变量为总生存期和安全性评估。
与继续使用他莫昔芬相比,换用阿那曲唑可显著降低疾病复发风险(风险比[HR],0.66;95%置信区间,0.44至1.00;P = 0.049),并改善总生存期(HR,0.53;95%置信区间,0.28至0.99;P = 0.045)。与继续使用他莫昔芬的患者相比,换用阿那曲唑的患者报告严重不良事件的较少(22.7%对30.8%),主要是因为他莫昔芬组中更多患者出现子宫内膜事件。阿那曲唑的总体安全性概况与既往报告一致,未发现新的安全问题。
作为辅助治疗服用他莫昔芬2年的绝经后女性,如果换用阿那曲唑而非继续接受他莫昔芬治疗,乳腺癌复发的可能性较小,且总生存期得到改善。