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A pooled analysis of case-control studies of thyroid cancer. III. Oral contraceptives, menopausal replacement therapy and other female hormones.

机译:甲状腺癌病例对照研究的汇总分析。三,口服避孕药,更年期替代疗法等女性荷尔蒙。

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OBJECTIVE: The relations between oral contraceptives (OC), hormone replacement therapy (HRT) for menopause, and other female hormone use and thyroid cancer risk was analyzed using the original data from 13 studies from North America, Asia and Europe. METHODS: Based on 2,132 cases and 3,301 controls, odds ratios (OR) and the corresponding 95% confidence intervals (CI) were obtained by conditional regression models, conditioning on study and age at diagnosis, and adjusting for age, radiation exposure and parity. RESULTS: Overall, 808 (38%) cases versus 1,290 (39%) controls had ever used OCs, corresponding to an OR of 1.2 (95% CI 1.0 to 1.4). There was no relation with duration of use, age at first use, or use before first birth. The OR was significantly increased for current OC users (OR = 1.5, 95% 1.0 to 2.1), but declined with increasing time since stopping (OR = 1.1 for > 10 years since stopping). The association was stronger for papillary cancers (OR = 1.6 for current users) than for other histologic types. No significant heterogeneity was observed across studies or geographic areas. Eight studies had data on HRT, for a total of 1,305 cases and 2,300 controls: 110 (8%) cases and 205 (9%) controls reported ever using HRT (OR = 0.8; 95% CI 0.6 to 1.1). The ORs were 1.6 (95% to 0.9 to 2.9) for use of fertility drugs, and 1.5 (95% CI 1.1 to 2.1) for lactation suppression treatment. CONCLUSIONS: The studies considered in these analyses include most of the epidemiological data on the role of exogenous hormone use in the etiology of thyroid cancer, and they provide reassuring evidence on the absence of an association of practical relevance. The moderate excess risk in current OC users, if not due to increased surveillance for thyroid masses among OC users, is similar to that described for breast cancer, and would imply a role of female hormones on thyroid cancer promotion. There was no indication of increased thyroid cancer risk 10 or more years after discontinuing OC use.
机译:目的:使用来自北美,亚洲和欧洲的13项研究的原始数据,分析了口服避孕药(OC),更年期激素替代疗法(HRT)和其他女性激素使用与甲状腺癌风险之间的关系。方法:基于2,132例病例和3,301例对照,通过条件回归模型,研究条件和诊断年龄以及对年龄,放射线暴露和均等进行调整,获得比值比(OR)和相应的95%置信区间(CI)。结果:总体上,有808(38%)例患者与1,290(39%)对照者曾经使用过OC,对应于OR为1.2(95%CI为1.0至1.4)。与使用时间,首次使用年龄或第一次生育前使用没有关系。当前OC用户的OR显着增加(OR = 1.5,95%1.0到2.1),但随着停止时间的增加而下降(停止10年后OR = 1.1)。与其他组织学类型相比,乳头状癌的相关性更强(当前使用者的OR = 1.6)。在研究或地理区域内未观察到明显的异质性。八项研究获得了有关HRT的数据,总共有1,305例病例和2,300例对照:110例(8%)病例和205例(9%)曾经使用HRT报道过对照(OR = 0.8; 95%CI 0.6至1.1)。使用生育药的OR为1.6(95%为0.9至2.9),而抑制泌乳的OR为1.5(95%CI 1.1至2.1)。结论:这些分析中考虑的研究包括有关外源激素使用在甲状腺癌病因学中作用的大多数流行病学数据,并且它们为缺乏实际相关性的研究提供了令人放心的证据。当前OC使用者的中度过度风险(如果不是由于增加了OC使用者对甲状腺肿块的监测),与乳腺癌中描述的相似,并且暗示女性荷尔蒙在甲状腺癌的促进中发挥了作用。停止使用OC后10年或更长时间,没有迹象表明甲状腺癌风险增加。

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