Suppr超能文献

激素替代疗法与肿瘤形成之间的联系。

Links between hormone replacement therapy and neoplasia.

作者信息

Hulka B S

机构信息

Department of Epidemiology, School of Public Health, University of North Carolina, Chapel Hill 27599-7400.

出版信息

Fertil Steril. 1994 Dec;62(6 Suppl 2):168S-175S.

PMID:7958013
Abstract

OBJECTIVE

To evaluate the literature on exogenous estrogens and progestins on risk of breast and endometrial cancers.

DESIGN

Review of epidemiologic literature.

SETTING

Population- and hospital-based studies.

SUBJECTS

Postmenopausal women.

INTERVENTIONS

Sex steroid hormone in hormone replacement regimens.

MAIN OUTCOME MEASURES

Breast carcinoma and endometrial carcinoma.

RESULTS

Estrogens cause cell proliferation in in vitro systems and enhance tumor formation in carcinogen-exposed animal models. Estrogen effects in humans vary by tissue type, exposure patterns, and subject groups. Doses commonly used for estrogen replacement therapy (ERT) are sufficient to cause proliferation, hyperplasia, and carcinoma of the endometrium. After 10 to 15 years of estrogen use, endometrial cancer risk increases nearly 10-fold, but the cancers produced are generally of low grade and stage with an excellent prognosis. Adding a progestin for > or = 10 d/mo reduces or eliminates the estrogen-induced risk. Breast tissue responds differently to sex steroid hormones. Long-term estrogen use increases breast cancer risk modestly (relative risk approximately 1.3 to 1.5). Particular subgroups, such as those with family history, benign proliferative disease, or late natural menopause, may experience greater risk. None of these characteristics are sufficiently well defined to be clear-cut contraindications to ERT. Adding a progestin does not improve the situation; relative risks may be higher for estrogen plus progestin than for estrogen alone. The effect of low dose progestin, e.g., 2.5 mg Provera, administered continuously with the estrogen, is not known. A small increase in relative risk has a large impact on number of women developing breast cancer because of the high baseline rates. For U.S. women age 65, the baseline rate is 210 new cases per 100,000 women per year. A relative risk as small as 1.2 increases a women's chances of developing breast cancer each year from 1 in 250 to 1 in 200.

摘要

目的

评估关于外源性雌激素和孕激素与乳腺癌及子宫内膜癌风险的文献。

设计

流行病学文献综述。

研究背景

基于人群和医院的研究。

研究对象

绝经后女性。

干预措施

激素替代方案中的性甾体激素。

主要观察指标

乳腺癌和子宫内膜癌。

结果

雌激素在体外系统中可导致细胞增殖,并在致癌物暴露的动物模型中增强肿瘤形成。雌激素对人类的影响因组织类型、暴露模式和研究对象群体而异。雌激素替代疗法(ERT)常用剂量足以导致子宫内膜增殖、增生和癌变。使用雌激素10至15年后,子宫内膜癌风险增加近10倍,但所产生的癌症通常为低级别和低分期,预后良好。每月添加孕激素≥10天可降低或消除雌激素诱导的风险。乳腺组织对性甾体激素的反应不同。长期使用雌激素会适度增加乳腺癌风险(相对风险约为1.3至1.5)。特定亚组,如具有家族病史、良性增生性疾病或自然绝经较晚的女性,可能面临更高风险。这些特征均未明确到足以成为ERT的明确禁忌证。添加孕激素并不能改善这种情况;雌激素加孕激素的相对风险可能高于单独使用雌激素。低剂量孕激素(如2.5mg醋酸甲羟孕酮)与雌激素持续联合使用的效果尚不清楚。由于基线发病率高,相对风险的小幅增加对患乳腺癌女性的数量有很大影响。对于65岁的美国女性,基线发病率为每年每10万名女性中有210例新病例。低至1.2的相对风险会使女性每年患乳腺癌的几率从250分之一增加到200分之一。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验