Depo-Provera and Breast Cancer: Epidemiology/Pathology
Depo-Provera and Breast Cancer: Epidemiology/Pathology
批准号:
7125959
负责人:
Christopher I Li
金额:
$65.87万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-26 至 2010-06-30
中文摘要
描述(由申请人提供):注射避孕药醋酸甲羟孕酮(DMPA) (Depo-Provera)是世界各地妇女常用的,它含有与美国绝经后妇女服用的雌激素和黄体酮激素联合治疗(CHT)方案中最常用的黄体酮。最近几项研究的数据表明,CHT增加了女性患乳腺癌的风险,而CHT中的黄体酮成分可能对这种风险的增加尤为重要。然而,关于DMPA和乳腺癌风险之间关系的数据有限。现有证据表明,目前使用DMPA与乳腺癌风险增加1.5至1.65倍有关。然而,由于这些研究存在方法学上的局限性(样本量和/或研究设计问题),因此需要对DMPA使用与乳腺癌之间的关系进行更多的研究,因为这些研究都没有在美国进行,因此尚不清楚这些结果是否适用于美国女性(因为各国的生殖和避孕模式差异很大),而且对DMPA促进乳腺癌的机制知之甚少。即使我们发现DMPA和乳腺癌风险之间没有关联,这项研究也是值得的,因为在这种情况下,使用DMPA的妇女可以放心,使用同样的药物,被认为是乳腺癌的原因,当作为注射避孕药服用时,不会增加她们患乳腺癌的风险。
英文摘要
DESCRIPTION (provided by applicant): The injectable contraceptive depot medroxy-progesterone acetate (DMPA) (Depo-Provera) is commonly used by women worldwide, and it contains the same progestin that is most commonly used in combined estrogen and progestin hormonal therapy (CHT) regimens taken by postmenopausal women in the United States. Data from several recent studies indicate that CHT increases a woman's risk of breast cancer, and that the progestin component of CHT may be particularly important with respect to this increased risk. There are limited data on the relationship between DMPA and breast cancer risk though. The available evidence suggests that current DMPA use is associated with a 1.5 to 1.65-fold increased risk of breast cancer. However, additional studies of the relationship between DMPA use and breast cancer are needed because these studies had methodologic limitations (sample size and/or study design issues), none were conducted in the U.S. and so it is unclear whether or not these results are generalizable to U.S. women (since reproductive and contraceptive patterns vary widely by country), and little is known about mechanisms through which DMPA promotes breast cancer. This study is worthwhile even if we find that there is no association between DMPA and breast cancer risk, since in this case women using DMPA will be reassured that using the same drug that has been implicated as a cause of breast cancer does not also increase their breast cancer risk when taken as an injectable contraceptive.
Herein we propose a case-control study of 1,000 women aged 20-44 who have been diagnosed with breast cancer and 1,000 population-based controls who reside in the Seattle-Puget Sound area. The specific hypotheses to be tested are: (1) Is DMPA use associated with an increased risk of breast cancer in premenopausal women 20-44? Does the duration and/or recency of DMPA use influence the magnitude of this association?; (2) Do demographic, reproductive, or anthropometric characteristics, such as parity and body mass index, modify this association?; and (3) Does the association between DMPA and breast cancer risk vary by histologic type or by the expression of steroid receptors including ERq, ERft, and PR?
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会议论文
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海外基金