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首页> 外文期刊>Cancer epidemiology, biomarkers and prevention: A publication of the American Association for Cancer Research >Relationship between menopausal hormone therapy and risk of ductal, lobular, and ductal-lobular breast carcinomas.
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Relationship between menopausal hormone therapy and risk of ductal, lobular, and ductal-lobular breast carcinomas.

机译:更年期激素治疗与导管癌,小叶癌和导管小叶癌风险之间的关系。

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Combined estrogen and progestin hormone therapy (CHT) increases breast cancer risk, but this risk varies by breast cancer type. Several studies indicate that CHT is more strongly related to lobular carcinoma risk than to ductal carcinoma risk, but these studies have been limited in their assessments of recency and duration of use, and none included a centralized pathology review. We conducted a population-based case-control study consisting of 324 lobular, 196 ductal-lobular, and 524 ductal cases diagnosed from 2000 to 2004 and 469 controls ages 55 to 74 years old. Tissue specimens were centrally reviewed for 83% of cases. Associations between hormone use and breast cancer risk were evaluated using polytomous logistic regression. Current CHT users had 2.7-fold [95% confidence interval (95% CI), 1.7-4.2] and 3.3-fold (95% CI, 2.0-5.7) elevated risks of lobular and ductal-lobular carcinomas, respectively, regardless of tumor stage, size, or nodal status. Elevations in risk were observed only among users of CHT for > or =3 years. Among ductal-lobular cases, CHT increased risk of tumors that were > or =50% lobular (odds ratio, 4.8; 95% CI, 2.1-11.1) but not tumors that were <50% lobular (odds ratio, 1.9; 95% CI, 0.9-4.1). Current CHT users for > or =3 years have a substantially increased risk of lobular carcinomas. Although lobular carcinomas are less common than ductal carcinomas ( approximately 16% versus 70% of all invasive breast cancers in the United States), this duration is shorter than the 5 years of use widely cited to be needed to confer an increased risk of breast cancer overall. Further studies focusing on the etiology of lobular carcinomas are needed.
机译:雌激素和孕激素联合治疗(CHT)会增加患乳腺癌的风险,但是这种风险因乳腺癌类型而异。几项研究表明,CHT与小叶癌风险的关系比与导管癌风险的关系更强,但这些研究对新近度和使用时间的评估受到限制,并且都没有进行集中的病理学检查。我们进行了一项基于人群的病例对照研究,包括2000年至2004年诊断出的324例小叶,196例导管小叶和524例导管病例,以及469例年龄在55至74岁之间的对照者。集中检查了83%的组织标本。使用多因素逻辑回归评估激素使用与乳腺癌风险之间的关联。目前的CHT使用者分别将小叶癌和导管小叶癌的风险提高2.7倍[95%置信区间(95%CI),1.7-4.2]和3.3倍(95%CI,2.0-5.7)高风险阶段,大小或节点状态。仅在CHT使用者中≥3年才观察到风险升高。在导管小叶病例中,CHT增加了>或= 50%小叶的肿瘤(几率,4.8; 95%CI,2.1-11.1)的风险,但不增加<50%小叶的肿瘤(几率,1.9; 95%)的风险CI,0.9-4.1)。当前使用CHT的时间大于或等于3年的人,患小叶癌的风险大大增加。尽管小叶癌不如导管癌常见(在美国,约占16%,而在所有浸润性乳腺癌中占70%),但该持续时间短于被广泛认为会增加患乳腺癌风险的5年使用时间总体。需要针对小叶癌病因的进一步研究。

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