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首页> 外文期刊>The Lancet >Use of luteinising-hormone-releasing hormone agonists as adjuvant treatment in premenopausal patients with hormone-receptor-positive breast cancer: a meta-analysis of individual patient data from randomised adjuvant trials.
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Use of luteinising-hormone-releasing hormone agonists as adjuvant treatment in premenopausal patients with hormone-receptor-positive breast cancer: a meta-analysis of individual patient data from randomised adjuvant trials.

机译:黄体生成激素释放激素激动剂在绝经前激素受体阳性乳腺癌患者中的辅助治疗:对来自随机佐剂试验的单个患者数据的荟萃分析。

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摘要

BACKGROUND: Several trials have been done to assess treatment of premenopausal breast cancer with luteinising-hormone-releasing hormone (LHRH) agonists, but results have been inconclusive, especially for patients with hormone-receptor-positive cancer. METHODS: We collected individual patients' data from published trials and did analyses focused on women with tumours positive for oestrogen receptor, progesterone receptor, or both. The main endpoints were recurrence and death after recurrence. FINDINGS: We obtained data for 11 906 premenopausal women with early breast cancer randomised in 16 trials. When used as the only systemic adjuvant treatment, LHRH agonists did not significantly reduce recurrence (28.4% relative reduction, 95% CI consistent with 50.5% reduction to 3.5% increase, p=0.08) or death after recurrence (17.8%, 52.8% reduction to 42.9% increase, p=0.49) in hormone-receptor-positive cancers. Addition of LHRH agonists to tamoxifen, chemotherapy, or both reduced recurrence by 12.7% (2.4-21.9,p=0.02); and death after recurrence by 15.1% (1.8-26.7, p=0.03). LHRH agonists showed similar efficacy to chemotherapy (recurrence 3.9% increase, 7.7% reduction to 17.0% increase; death after recurrence 6.7% reduction, 20.7% reduction to 9.6% increase; both not significant). No trials had assessed an LHRH agonist versus chemotherapy with tamoxifen in both arms. LHRH agonists were ineffective in hormone-receptor-negative tumours. INTERPRETATION: LHRH agonists provide an additional class of agents for treatment of premenopausal women with hormone-receptor-positive breast cancer. Optimum duration of use is unknown.
机译:背景:已经进行了数项评估黄体激素释放激素(LHRH)激动剂对绝经前乳腺癌治疗的试验,但结果尚无定论,尤其是对于激素受体阳性的患者。方法:我们从已发表的试验中收集了个别患者的数据,并进行了针对雌激素受体,孕激素受体或两者均阳性的肿瘤女性的分析。主要终点是复发和复发后死亡。结果:我们获得了11 906名绝经前乳腺癌早期女性的数据,该数据随机分配到16个试验中。当用作唯一的全身性辅助治疗时,LHRH激动剂并没有显着降低复发率(相对降低28.4%,CI降低95%,CI降低50.5%至3.5%,P = 0.08)或复发后死亡(降低17.8%,52.8%)。在激素受体阳性癌症中增加42.9%,p = 0.49)。在他莫昔芬,化学疗法或两者中加用LHRH激动剂可使复发减少12.7%(2.4-21.9,p = 0.02);复发后的死亡率为15.1%(1.8-26.7,p = 0.03)。 LHRH激动剂显示出与化疗相似的疗效(复发增加3.9%,减少7.7%至17.0%;复发后死亡减少6.7%,减少20.7%至9.6%;两者均不显着)。尚无试验评估LHRH激动剂与化疗联合他莫昔芬的作用。 LHRH激动剂在激素受体阴性肿瘤中无效。解释:LHRH激动剂为激素受体阳性乳腺癌的绝经前妇女提供了另一类药物。最佳使用期限未知。

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