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Self-reported medication use validated through record linkage to national prescribing data.通过与国家处方数据的记录链接验证自我报告的药物使用情况。
J Clin Epidemiol. 2018 Feb;94:132-142. doi: 10.1016/j.jclinepi.2017.10.013. Epub 2017 Oct 31.
2
Menopausal hormone therapy and breast cancer: what is the true size of the increased risk?更年期激素疗法与乳腺癌:风险增加的真实程度究竟如何?
Br J Cancer. 2016 Aug 23;115(5):607-15. doi: 10.1038/bjc.2016.231. Epub 2016 Jul 28.
3
Association Between Menopausal Estrogen-Only Therapy and Ovarian Carcinoma Risk.绝经后单纯雌激素治疗与卵巢癌风险之间的关联。
Obstet Gynecol. 2016 May;127(5):828-836. doi: 10.1097/AOG.0000000000001387.
4
African Americans and Hispanics Remain at Lower Risk of Ovarian Cancer Than Non-Hispanic Whites after Considering Nongenetic Risk Factors and Oophorectomy Rates.在考虑非遗传风险因素和卵巢切除率后,非裔美国人和西班牙裔患卵巢癌的风险仍低于非西班牙裔白人。
Cancer Epidemiol Biomarkers Prev. 2015 Jul;24(7):1094-100. doi: 10.1158/1055-9965.EPI-15-0023. Epub 2015 Apr 14.
5
Menopausal hormone use and ovarian cancer risk: individual participant meta-analysis of 52 epidemiological studies.更年期激素使用与卵巢癌风险:52项流行病学研究的个体参与者荟萃分析
Lancet. 2015 May 9;385(9980):1835-42. doi: 10.1016/S0140-6736(14)61687-1. Epub 2015 Feb 13.
6
Sun exposure and risk of epithelial ovarian cancer.日光暴露与上皮性卵巢癌风险。
Cancer Causes Control. 2012 Dec;23(12):1985-94. doi: 10.1007/s10552-012-0076-x. Epub 2012 Oct 12.
7
Ovarian cancer and menopausal hormone therapy in the NIH-AARP diet and health study.美国国立卫生研究院-美国退休人员协会饮食与健康研究中的卵巢癌与绝经后激素治疗。
Br J Cancer. 2012 Sep 25;107(7):1181-7. doi: 10.1038/bjc.2012.397. Epub 2012 Aug 28.
8
Mucinous carcinomas of the ovary and colorectum: different organ, same dilemma.卵巢和结直肠黏液性癌:不同器官,同样困境。
Lancet Oncol. 2011 Oct;12(11):1071-80. doi: 10.1016/S1470-2045(11)70058-4. Epub 2011 May 25.
9
Contraception methods, beyond oral contraceptives and tubal ligation, and risk of ovarian cancer.除了口服避孕药和输卵管结扎术以外的避孕方法与卵巢癌风险。
Ann Epidemiol. 2011 Mar;21(3):188-96. doi: 10.1016/j.annepidem.2010.10.002. Epub 2010 Dec 15.
10
Pooled analysis of the association of PTGS2 rs5275 polymorphism and NSAID use with invasive ovarian carcinoma risk.PTGS2 rs5275 多态性与 NSAID 使用与侵袭性卵巢癌风险的关联的汇总分析。
Cancer Causes Control. 2010 Oct;21(10):1731-41. doi: 10.1007/s10552-010-9602-x. Epub 2010 Jun 18.

雌激素加孕激素激素治疗与卵巢癌:复杂关系的探索。

Estrogen Plus Progestin Hormone Therapy and Ovarian Cancer: A Complicated Relationship Explored.

机构信息

From the Department of Public Health, California State University, Fullerton, Fullerton, CA.

Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI.

出版信息

Epidemiology. 2020 May;31(3):402-408. doi: 10.1097/EDE.0000000000001175.

DOI:10.1097/EDE.0000000000001175
PMID:32028322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7584395/
Abstract

BACKGROUND

Menopausal estrogen-alone therapy is a risk factor for endometrial and ovarian cancers. When a progestin is included with the estrogen daily (continuous estrogen-progestin combined therapy), there is no increased risk of endometrial cancer. However, the effect of continuous estrogen-progestin combined therapy on risk of ovarian cancer is less clear.

METHODS

We pooled primary data from five population-based case-control studies in the Ovarian Cancer Association Consortium, including 1509 postmenopausal ovarian cancer cases and 2295 postmenopausal controls. Information on previous menopausal hormonal therapy use, as well as ovarian cancer risk factors, was collected using in-person interviews. Logistic regression was used to assess the association between use of continuous estrogen-progestin combined therapy and risk of ovarian cancer by duration and recency of use and disease histotype.

RESULTS

Ever postmenopausal use of continuous estrogen-progestin combined therapy was not associated with increased risk of ovarian cancer overall (OR = 0.85, 95% CI = 0.72, 1.0). A decreased risk was observed for mucinous ovarian cancer (OR = 0.40, 95% CI = 0.18, 0.91). The other main ovarian cancer histotypes did not show an association (endometrioid: OR = 0.86, 95% CI = 0.57, 1.3, clear cell: OR = 0.68, 95% CI = 0.40, 1.2; serous: OR = 0.98, 95% CI = 0.80, 1.2).

CONCLUSIONS

Given that estrogen-alone therapy has been shown to be associated with increased risk of ovarian cancer, these findings are consistent with the hypothesis that adding a progestin each day ameliorates the carcinogenic effects of estrogen on the cells of origin for all histotypes of ovarian cancer.

摘要

背景

绝经后单独使用雌激素治疗是子宫内膜癌和卵巢癌的一个风险因素。当雌激素与孕激素每天同时使用(连续雌激素-孕激素联合治疗)时,子宫内膜癌的风险不会增加。然而,连续雌激素-孕激素联合治疗对卵巢癌风险的影响尚不清楚。

方法

我们汇总了卵巢癌协会联盟中五个基于人群的病例对照研究的原始数据,包括 1509 例绝经后卵巢癌病例和 2295 例绝经后对照。使用面对面访谈收集了关于以前绝经激素治疗使用情况以及卵巢癌危险因素的信息。使用逻辑回归评估了连续雌激素-孕激素联合治疗的使用与卵巢癌风险之间的关联,按使用时间长短和使用时间的新近程度以及疾病组织学类型进行评估。

结果

绝经后持续使用连续雌激素-孕激素联合治疗与卵巢癌总体风险增加无关(OR=0.85,95%CI=0.72,1.0)。观察到黏液性卵巢癌的风险降低(OR=0.40,95%CI=0.18,0.91)。其他主要的卵巢癌组织学类型没有显示出关联(子宫内膜样:OR=0.86,95%CI=0.57,1.3;透明细胞:OR=0.68,95%CI=0.40,1.2;浆液性:OR=0.98,95%CI=0.80,1.2)。

结论

鉴于雌激素单独治疗已被证明与卵巢癌风险增加有关,这些发现与以下假设一致,即每天添加孕激素可减轻雌激素对所有卵巢癌组织学类型起源细胞的致癌作用。