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口服避孕药与肝癌。多中心国际肝脏肿瘤研究(MILTS)的结果。

Oral contraceptives and liver cancer. Results of the Multicentre International Liver Tumor Study (MILTS).

出版信息

Contraception. 1997 Nov;56(5):275-84.

PMID:9437555
Abstract

Many, but not all, previous epidemiological studies indicated a greater risk of hepatocellular cancer (HCC) in women who have used combined oral contraceptives for a long period of time, but no one has analyzed this risk based upon use of different formulations. It was decided to analyze specifically the risk of OC containing cyproterone acetate (CPA) after toxicological experiments in animals found hints for a potential genotoxicity. This report describes the risk associated with ever having used combined oral contraceptives (OC) among 317 cases of primary hepatocellular cancer (HCC) in women under age 65, compared with 1060 age-matched hospital and 719 population controls in a case-control study, which was conducted in six European countries. The adjusted odds ratio (unconditional logistic regression) for ever having used any OC was found to be 0.75 (0.54 to 1.03) when all cases were compared with all controls, and compared to hospital and population controls separately: 1.13 (0.86 to 1.48) and 0.78 (0.59 to 1.03), respectively. The adjusted odds ratios for OC containing all progestins of the CPA group were 0.89 (0.49 to 1.61); and 0.89 (0.37 to 2.18) for OC containing only CPA. There was no increase in risk for HCC with increasing duration of OC use among the different groups of OCs in the total group of cases with pooled controls. The risk estimates were not related to time since first or last use of any of the types of OCs considered. The most important risk factors for HCC were confirmed as a prior history of hepatitis B and C (adjusted odds ratio 3.1 (2.2; 4.3) and 37.9 (20.2; 70.9) for HBV and HCV, respectively). In the small subgroup of HCC cases without liver cirrhosis and with negative serology for HBV and HCV, there was evidence of an association with duration of OC use. No such trend was observed for the CPA group of OCs. Altogether, there is no evidence for an increased risk of HCC associated with CPA or CPA-like OCs. Oral contraceptives in the aggregate may enhance the risk of liver carcinomas not associated with HBV or HCV infection, but if so, this is an extremely rare adverse effect of their use.

摘要

许多(但并非全部)既往流行病学研究表明,长期使用复方口服避孕药的女性患肝细胞癌(HCC)的风险更高,但此前没有人根据不同配方的使用情况分析这种风险。在动物毒理学实验发现潜在遗传毒性的线索后,决定专门分析含有醋酸环丙孕酮(CPA)的口服避孕药的风险。本报告描述了在一项病例对照研究中,65岁以下女性原发性肝细胞癌(HCC)317例患者中曾经使用复方口服避孕药(OC)的相关风险,该研究在6个欧洲国家开展,将这些患者与1060名年龄匹配的医院对照和719名人群对照进行比较。当将所有病例与所有对照进行比较时,曾经使用任何口服避孕药的调整优势比(无条件逻辑回归)为0.75(0.54至1.03),与医院对照和人群对照分别比较时:分别为1.13(0.86至1.48)和0.78(0.59至1.03)。含有CPA组所有孕激素的口服避孕药的调整优势比为0.89(0.49至1.61);仅含有CPA的口服避孕药的调整优势比为0.89(0.37至2.18)。在合并对照的所有病例组中,不同类型口服避孕药组中,随着口服避孕药使用时间延长,HCC风险没有增加。风险估计与首次或最后使用任何所考虑类型口服避孕药后的时间无关。HCC最重要的风险因素被确认为既往有乙型和丙型肝炎病史(HBV和HCV的调整优势比分别为3.1(2.2;4.3)和37.9(20.2;70.9))。在没有肝硬化且HBV和HCV血清学阴性的HCC病例小亚组中,有证据表明与口服避孕药使用时间有关。对于CPA组口服避孕药未观察到这种趋势。总体而言,没有证据表明与CPA或类似CPA的口服避孕药相关的HCC风险增加。总体而言,口服避孕药可能会增加与HBV或HCV感染无关的肝癌风险,但即便如此,这也是其使用极为罕见的不良反应。

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