Jubelirer S J, Crowell E B
Cancer Care Center of Southern West Virginia, Charleston Area Medical Center.
W V Med J. 1992 Sep;88(9):399-401.
Female breast cancer is a major medical problem with significant public health ramifications. During the next decade, more than 1.5 million women in the United States will be newly diagnosed with invasive breast cancer. The Breast Cancer Prevention Trial (BCPT) is an NIH-sponsored study which will determine whether long-term tamoxifen therapy is effective in: 1) Preventing invasive breast cancer, 2) Lowering the incidence of fatal and nonfatal myocardial infarction, and 3) Reducing the incidence of bone fractures. Sixteen thousand women, including at least 100 from West Virginia who are > or = 35 years of age at increased risk for breast cancer, will be randomized between placebo and tamoxifen during a two-year period. For each participant, the annual and lifetime probability of developing breast cancer will be estimated utilizing a computerized model of risk assessment. The placebo or tamoxifen will be administered for at least five years. Toxicity, compliance, monitoring of quality-of-life assessment, and lipid and lipoprotein evaluations are major components of this trial.
女性乳腺癌是一个重大的医学问题,对公众健康有重大影响。在未来十年,美国将有超过150万女性被新诊断为浸润性乳腺癌。乳腺癌预防试验(BCPT)是一项由美国国立卫生研究院资助的研究,该研究将确定长期服用他莫昔芬治疗是否在以下方面有效:1)预防浸润性乳腺癌;2)降低致命和非致命心肌梗死的发病率;3)降低骨折的发病率。16000名女性,包括至少100名来自西弗吉尼亚州、年龄≥35岁且患乳腺癌风险增加的女性,将在两年内被随机分为服用安慰剂组和他莫昔芬组。对于每位参与者,将使用计算机化风险评估模型估计患乳腺癌的年度和终生概率。安慰剂或他莫昔芬将至少服用五年。毒性、依从性、生活质量评估监测以及血脂和脂蛋白评估是该试验的主要组成部分。