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一项在绝经前早期乳腺癌女性中辅助化疗后应用他莫昔芬的随机安慰剂对照研究(加拿大国家癌症研究所-临床试验组试验,MA.12)。

A randomized placebo-controlled study of tamoxifen after adjuvant chemotherapy in premenopausal women with early breast cancer (National Cancer Institute of Canada--Clinical Trials Group Trial, MA.12).

机构信息

Department of Medical Oncology, Tom Baker Cancer Centre, Calgary, Alberta.

Department of Medical Oncology, Sunnybrook Odette Cancer Centre, Toronto, Ontario.

出版信息

Ann Oncol. 2010 Feb;21(2):283-290. doi: 10.1093/annonc/mdp326. Epub 2009 Jul 23.

Abstract

BACKGROUND

In the early 1990s, the role of adjuvant tamoxifen in premenopausal women with early breast cancer (EBC) was not established. Similarly, optimum timing relative to adjuvant chemotherapy and efficacy of tamoxifen in hormone receptor-negative tumors were unclear.

PATIENTS AND METHODS

Premenopausal women with EBC, any hormone receptor status, after surgery received standard adjuvant chemotherapy [doxorubicin (adriamycin)/cyclophosphamide, cyclophosphamide/methotrexate/5-fluorouracil, or cyclophosphamide/epirubicin/5-fluorouracil] followed by randomization to tamoxifen or placebo for 5 years. Outcomes were overall survival (OS), disease-free survival (DFS), toxicity, and compliance with therapy.

RESULTS

Median follow-up for 672 women was 9.7 years. Multivariate analysis showed improved DFS [78.2% versus 71.3% at 5 years; hazard ratio (HR) 0.77; P = 0.056] and a trend for improved OS (86.6% versus 82.1% at 5 years; HR 0.78; P = 0.12). There was no evidence of greater benefit for the receptor-positive subgroup. Compliance with treatment was suboptimal in both arms, with 103 (31%) women on tamoxifen and 70 (21%) on placebo-stopping therapy early because of toxicity, refusal, or other choices.

CONCLUSIONS

Adjuvant tamoxifen, given after chemotherapy to premenopausal women with EBC, improved 5-year DFS. Poor compliance may have reduced treatment efficacy.

摘要

背景

在 20 世纪 90 年代早期,辅助他莫昔芬在绝经前早期乳腺癌(EBC)患者中的作用尚未确定。同样,相对于辅助化疗的最佳时机以及激素受体阴性肿瘤中他莫昔芬的疗效也不明确。

患者和方法

接受手术治疗的绝经前 EBC 患者,无论激素受体状态如何,均接受标准辅助化疗[阿霉素(多柔比星)/环磷酰胺、环磷酰胺/甲氨蝶呤/5-氟尿嘧啶或环磷酰胺/表柔比星/5-氟尿嘧啶],然后随机分为他莫昔芬或安慰剂组,接受 5 年的治疗。主要研究终点为总生存(OS)、无病生存(DFS)、毒性和治疗依从性。

结果

672 例患者的中位随访时间为 9.7 年。多变量分析显示 DFS 得到改善[5 年时分别为 78.2%和 71.3%;风险比(HR)为 0.77;P=0.056],OS 也有改善趋势(5 年时分别为 86.6%和 82.1%;HR 为 0.78;P=0.12)。受体阳性亚组并未显示出更大的获益。两组的治疗依从性均不理想,103 例(31%)接受他莫昔芬治疗的患者和 70 例(21%)接受安慰剂治疗的患者因毒性、拒绝或其他原因早期停止治疗。

结论

在化疗后,辅助他莫昔芬用于绝经前 EBC 患者,可改善 5 年 DFS。较差的依从性可能降低了治疗效果。

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