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首页> 外文期刊>Journal of the National Cancer Institute >Estimates of the number of US women who could benefit from tamoxifen for breast cancer chemoprevention.
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Estimates of the number of US women who could benefit from tamoxifen for breast cancer chemoprevention.

机译:估计可以从他莫昔芬中受益的美国女性乳腺癌化学预防人数。

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BACKGROUND: The Breast Cancer Prevention Trial demonstrated that tamoxifen treatment produced a 49% reduction in the risk of invasive breast cancer among women at elevated risk for the disease. The U.S. Food and Drug Administration (FDA) subsequently approved tamoxifen for women aged 35 years or older with a 5-year breast cancer risk of 1.67% or higher for breast cancer chemoprevention. However, tamoxifen use has been associated with adverse outcomes, and not all eligible women have a positive benefit/risk ratio. METHODS: We used weighted data from the year 2000 National Health Interview Survey Cancer Control Module to estimate the total number of U.S. women, aged 35-79 years, who were eligible for tamoxifen chemoprevention based on the FDA eligibility criteria. We also estimated the numbers of white and black women who would benefit from tamoxifen chemoprevention on the basis of a positive benefit/risk index developed by Gail et al. RESULTS: Of the 65,826,074 women aged 35-79 years without reported breast cancer in the United States in 2000, 10,232 816 women (15.5%, 95% confidence interval [CI] = 14.7% to 16.3%) would be eligible for tamoxifen chemoprevention. The percentage of U.S. women who would be eligible varied dramatically by race, with 18.7% (95% CI = 17.8% to 19.7%) of white women, 5.7% (95% CI = 4.3% to 7.5%) of black women, and 2.9% (95% CI = 2.1% to 3.9%) of Hispanic women being eligible. Of the 50,104,829 white U.S. women aged 35-79 years, 2,431,911 (4.9%, 95% CI = 4.3% to 5.4%) would have a positive benefit/risk index for tamoxifen chemoprevention. Of the 7,481,779 black U.S. women aged 35-79 years, only 42,768 (0.6%, 95% CI = 0.2% to 1.3%) would have a positive benefit/risk index. Among white women, 28,492 (95% CI = 24,693 to 32,292) breast cancers would be prevented or deferred if those women who have a positive net benefit index took tamoxifen over the next 5 years. CONCLUSION: A substantial percentage of U.S. women would be eligible for tamoxifen chemoprevention according to FDA criteria, but a much smaller percentage would have an estimated net benefit. Nevertheless, this latter percentage corresponds to more than two million women.
机译:背景:乳腺癌预防试验表明,他莫昔芬治疗可使罹患这种疾病的风险较高的妇女的浸润性乳腺癌风险降低49%。随后,美国食品药品监督管理局(FDA)批准了他莫昔芬用于35岁或以上的女性,其5年乳腺癌的化学预防风险为1.67%或更高。但是,他莫昔芬的使用已与不良后果相关联,并非所有符合条件的妇女的获益/风险比均为正。方法:我们使用了来自2000年美国国家健康访问调查癌症控制模块的加权数据,以根据FDA资格标准估算了符合三苯氧胺化学预防条件的35-79岁美国妇女的总数。我们还根据盖尔(Gail)等人开发的正效益/风险指数,估计了将受益于他莫昔芬化学预防的白人和黑人妇女的数量。结果:在2000年的美国65,826,074名35-79岁未报告乳腺癌的妇女中,有10,232,816名妇女(15.5%,95%的置信区间[CI] = 14.7%至16.3%)有资格接受他莫昔芬的化学预防。符合资格的美国女性百分比因种族而异,白人女性为18.7%(95%CI = 17.8%至19.7%),黑人女性为5.7%(95%CI = 4.3%至7.5%),以及符合资格的西班牙裔女性占2.9%(95%CI = 2.1%至3.9%)。在50,104,829名35-79岁的美国白人女性中,2,431,911(4.9%,95%CI = 4.3%至5.4%)的他莫昔芬化学预防获益/风险指数为正。在美国的7,481,779名35-79岁的黑人女性中,只有42,768(0.6%,95%CI = 0.2%至1.3%)的受益/风险指数为正。在白人妇女中,如果那些净收益指数为正的妇女在未来5年内服用他莫昔芬,则将预防或推迟28,492例乳腺癌(95%CI = 24,693至32,292例)。结论:根据FDA标准,相当大比例的美国妇女有资格接受他莫昔芬的化学预防,但估计比例少得多。然而,后一个百分比对应于超过200万妇女。

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