Hackshaw Allan, Baum Michael, Fornander Tommy, Nordenskjold Bo, Nicolucci Antonio, Monson Kathryn, Forsyth Sharon, Reczko Krystyna, Johansson Ulla, Fohlin Helena, Valentini Miriam, Sainsbury Richard
Cancer Research UK & UCL Cancer Trials Centre, University College London, 90 Tottenham Court Rd, London W1T 4TJ, UK.
J Natl Cancer Inst. 2009 Mar 4;101(5):341-9. doi: 10.1093/jnci/djn498. Epub 2009 Feb 24.
Systematic reviews have found that luteinizing hormone-releasing hormone (LHRH) agonists are effective in treating premenopausal women with early breast cancer.
We conducted long-term follow-up (median 12 years) of 2706 women in the Zoladex In Premenopausal Patients (ZIPP), which evaluated the LHRH agonist goserelin (3.6 mg injection every 4 weeks) and tamoxifen (20 or 40 mg daily), given for 2 years. Women were randomly assigned to receive each therapy alone, both, or neither, after primary therapy (surgery with or without radiotherapy/chemotherapy). Hazard ratios and absolute risk differences were used to assess the effect of goserelin treatment on event-free survival (breast cancer recurrence, new tumor or death), overall survival, risk of recurrence of breast cancer, and risk of dying from breast cancer, in the presence or absence of tamoxifen.
Fifteen years after the initiation of treatment, for every 100 women not given tamoxifen, there were 13.9 (95% confidence interval [CI] = 17.5 to 19.4) fewer events among those who were treated with goserelin compared with those who were not treated with goserelin. However, among women who did take tamoxifen, there were 2.8 fewer events (95% CI = 7.7 fewer to 2.0 more) per 100 women treated with goserelin compared with those not treated with goserelin. The risk of dying from breast cancer was also reduced at 15 years: For every 100 women given goserelin, the number of breast cancer deaths was lower by 2.6 (95% CI = 6.6 fewer to 2.1 more) and 8.5 (95% CI = 2.2 to 13.7) in those who did and did not take tamoxifen, respectively, although in the former group the difference was not statistically significant.
Two years of goserelin treatment was as effective as 2 years of tamoxifen treatment 15 years after starting therapy. In women who did not take tamoxifen, there was a large benefit of goserelin treatment on survival and recurrence, and in women who did take tamoxifen, there was a marginal potential benefit on these outcomes when goserelin was added.
系统评价发现,促黄体生成素释放激素(LHRH)激动剂对治疗绝经前早期乳腺癌女性有效。
我们对绝经前患者使用戈舍瑞林(ZIPP)研究中的2706名女性进行了长期随访(中位时间12年),该研究评估了LHRH激动剂戈舍瑞林(每4周注射3.6毫克)和他莫昔芬(每日20或40毫克),给药2年。在进行初始治疗(手术加或不加放疗/化疗)后,女性被随机分配单独接受每种治疗、两种治疗或不接受任何治疗。在有或没有他莫昔芬的情况下,使用风险比和绝对风险差异来评估戈舍瑞林治疗对无事件生存期(乳腺癌复发、新发肿瘤或死亡)、总生存期、乳腺癌复发风险和死于乳腺癌风险的影响。
治疗开始15年后,对于每100名未接受他莫昔芬治疗的女性,接受戈舍瑞林治疗的女性与未接受戈舍瑞林治疗的女性相比,事件发生率减少了13.9例(95%置信区间[CI]=17.5至19.4)。然而,在接受他莫昔芬治疗的女性中,每100名接受戈舍瑞林治疗的女性与未接受戈舍瑞林治疗的女性相比,事件发生率减少了2.8例(95%CI=减少7.7例至增加2.0例)。15年时死于乳腺癌的风险也有所降低:对于每100名接受戈舍瑞林治疗的女性,在接受和未接受他莫昔芬治疗的女性中,乳腺癌死亡人数分别减少了2.6例(95%CI=减少6.6例至增加2.1例)和8.5例(95%CI=2.2至13.7),尽管在前一组中差异无统计学意义。
治疗开始15年后,两年的戈舍瑞林治疗与两年的他莫昔芬治疗效果相当。在未接受他莫昔芬治疗的女性中,戈舍瑞林治疗对生存和复发有很大益处,而在接受他莫昔芬治疗的女性中,添加戈舍瑞林对这些结果有一定潜在益处。