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雷洛昔芬治疗绝经后女性持续降低乳腺癌风险:MORE试验的4年结果。雷洛昔芬评估的多项结果。

Continued breast cancer risk reduction in postmenopausal women treated with raloxifene: 4-year results from the MORE trial. Multiple outcomes of raloxifene evaluation.

作者信息

Cauley J A, Norton L, Lippman M E, Eckert S, Krueger K A, Purdie D W, Farrerons J, Karasik A, Mellstrom D, Ng K W, Stepan J J, Powles T J, Morrow M, Costa A, Silfen S L, Walls E L, Schmitt H, Muchmore D B, Jordan V C, Ste-Marie L G

机构信息

Department of Epidemiology, University of Pittsburgh, PA 15261, USA.

出版信息

Breast Cancer Res Treat. 2001 Jan;65(2):125-34. doi: 10.1023/a:1006478317173.

Abstract

Raloxifene, a selective estrogen receptor modulator approved for the prevention and treatment of postmenopausal osteoporosis, has shown a significant reduction in breast cancer incidence after 3 years in this placebo-controlled, randomized clinical trial in postmenopausal women with osteoporosis. This article includes results from an additional annual mammogram at 4 years and represents 3,004 additional patient-years of follow-up in this trial. Breast cancers were ascertained through annual screening mammograms and adjudicated by an independent oncology review board. A total of 7,705 women were enrolled in the 4-year trial; 2,576 received placebo, 2,557 raloxifene 60 mg/day, and 2,572 raloxifene 120 mg/day. Women were a mean of 66.5-years old at trial entry, 19 years postmenopause, and osteoporotic (low bone mineral density and/or prevalent vertebral fractures). As of 1 November 1999, 61 invasive breast cancers had been reported and were confirmed by the adjudication board, resulting in a 72% risk reduction with raloxifene (relative risk (RR) 0.28, 95% confidence interval (CI) 0.17, 0.46). These data indicate that 93 osteoporotic women would need to be treated with raloxifene for 4 years to prevent one case of invasive breast cancer. Raloxifene reduced the risk of estrogen receptor-positive invasive breast cancer by 84% (RR 0.16, 95% CI 0.09, 0.30). Raloxifene was generally safe and well-tolerated, however, thromboembolic disease occurred more frequently with raloxifene compared with placebo (p=0.003). We conclude that raloxifene continues to reduce the risk of breast cancer in women with osteoporosis after 4 years of treatment, through prevention of new cancers or suppression of subclinical tumors, or both. Additional randomized clinical trials continue to evaluate this effect in postmenopausal women with osteoporosis, at risk for cardiovascular disease, and at high risk for breast cancer.

摘要

雷洛昔芬是一种已被批准用于预防和治疗绝经后骨质疏松症的选择性雌激素受体调节剂。在这项针对绝经后骨质疏松症女性的安慰剂对照随机临床试验中,雷洛昔芬在3年后显示出乳腺癌发病率显著降低。本文纳入了4年时额外的年度乳房X光检查结果,代表了该试验中额外3004患者年的随访。乳腺癌通过年度筛查乳房X光检查确定,并由独立的肿瘤学审查委员会进行判定。共有7705名女性参加了为期4年的试验;2576人接受安慰剂,2557人接受雷洛昔芬60毫克/天,2572人接受雷洛昔芬120毫克/天。试验开始时女性的平均年龄为66.5岁,绝经19年,患有骨质疏松症(低骨矿物质密度和/或既往椎体骨折)。截至1999年11月1日,已报告61例浸润性乳腺癌并经判定委员会确认,雷洛昔芬使风险降低了72%(相对风险(RR)0.28,95%置信区间(CI)0.17,0.46)。这些数据表明,93名骨质疏松症女性需要接受4年的雷洛昔芬治疗以预防1例浸润性乳腺癌。雷洛昔芬使雌激素受体阳性浸润性乳腺癌的风险降低了84%(RR 0.16,95%CI 0.09,0.30)。雷洛昔芬总体上安全且耐受性良好,然而,与安慰剂相比,雷洛昔芬治疗的患者血栓栓塞性疾病的发生率更高(p = 0.003)。我们得出结论,经过4年治疗,雷洛昔芬通过预防新发癌症或抑制亚临床肿瘤,或两者兼而有之,继续降低骨质疏松症女性患乳腺癌的风险。其他随机临床试验继续在有心血管疾病风险和乳腺癌高风险的绝经后骨质疏松症女性中评估这种效果。

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