Menopausal hormone therapy and breast cancer

IF 2.7 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Steroid Biochemistry and Molecular Biology Pub Date : 2014-07-01 DOI:10.1016/j.jsbmb.2013.06.010
Richard J. Santen
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引用次数: 48

Abstract

Observational and randomized controlled trial data have extensively examined the relationship between menopausal hormone therapy (MHT) and risk of developing breast cancer. A highly influential study from the Women's Health Initiative (WHI) in 2002 reported that a MHT regimen of conjugated equine estrogens and medroxyprogesterone acetate increased the risk of breast cancer by 26%. Later reports from the WHI indicated that a MHT regimen with conjugated equine estrogens alone decreased the risk of breast cancer by 23%. Critical re-examination of the WHI study noted that the average participant age was 63, that few women had symptoms, and that the WHI results might not apply to younger, symptomatic women shortly after menopause. Since the original publications, several post hoc analyses and observational studies have stimulated reconsideration of the WHI findings. Emphasis has been directed toward risks in younger women just entering the menopause, the subgroup who are most likely to be considering MHT use.

The goal of this treatise is to integrate available mechanistic and clinical information related to the use of estrogen alone or estrogen plus a progestogen for five years or less. These data suggest that estrogen alone neither decreases nor increases risk in younger women initiating therapy close to the time of menopause but decreases risk in older women. Both younger and older women experience an excess risk with estrogen plus a progestogen. The attributable risk in younger women is less in those with a low underlying Gail Model risk score. Effects of MHT on risk largely reflect actions on pre-existing, occult, undiagnosed breast cancers. Tumor kinetic models suggest that the pro-proliferative effects of estrogen plus a progestogen on occult tumors provide a mechanistic explanation for the increased risk with this therapy. Pro-apoptotic effects of estrogen alone may explain the reduction of breast cancer in women starting this therapy at an average age of 63 as reported in the WHI study.

This article is part of a Special Issue entitled ‘Menopause’.

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更年期激素治疗和乳腺癌
观察性和随机对照试验数据广泛地研究了绝经期激素治疗(MHT)与患乳腺癌风险之间的关系。2002年妇女健康倡议(WHI)的一项极具影响力的研究报告称,结合马雌激素和醋酸甲孕酮的MHT方案使乳腺癌的风险增加了26%。WHI后来的报告表明,单独结合马雌激素的MHT方案可降低23%的乳腺癌风险。对WHI研究的重要复查指出,参与者的平均年龄为63岁,很少有妇女出现症状,WHI的结果可能不适用于绝经后不久出现症状的年轻妇女。自最初的出版物以来,一些事后分析和观察性研究刺激了对WHI发现的重新考虑。重点一直指向刚刚进入更年期的年轻女性的风险,这一亚组最有可能考虑使用MHT。这篇论文的目的是整合现有的机制和临床信息有关使用雌激素单独或雌激素加孕激素5年或更短。这些数据表明,单独使用雌激素既不会降低也不会增加接近更年期开始治疗的年轻女性的风险,但会降低老年女性的风险。无论是年轻女性还是老年女性,雌激素加孕激素都有额外的风险。盖尔模型风险评分较低的年轻女性的归因风险较小。MHT对风险的影响在很大程度上反映了对已存在的、隐匿的、未确诊的乳腺癌的作用。肿瘤动力学模型表明,雌激素加孕激素对隐匿性肿瘤的促增殖作用为这种治疗增加风险提供了机制解释。据WHI研究报道,雌激素单独的促凋亡作用可以解释平均年龄为63岁的妇女开始这种治疗的乳腺癌减少。这篇文章是《更年期》特刊的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
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8.60
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2.40%
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113
审稿时长
46 days
期刊介绍: The Journal of Steroid Biochemistry and Molecular Biology is devoted to new experimental and theoretical developments in areas related to steroids including vitamin D, lipids and their metabolomics. The Journal publishes a variety of contributions, including original articles, general and focused reviews, and rapid communications (brief articles of particular interest and clear novelty). Selected cutting-edge topics will be addressed in Special Issues managed by Guest Editors. Special Issues will contain both commissioned reviews and original research papers to provide comprehensive coverage of specific topics, and all submissions will undergo rigorous peer-review prior to publication.
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