Gambrell R D
South Med J. 1984 Dec;77(12):1509-15. doi: 10.1097/00007611-198412000-00009.
Since the incidence of endometrial cancer among estrogen-treated women at Wilford Hall Air Force Medical Center was not increased as reported by others, a prospective study was begun in 1975. With this data base, the cases of breast and endometrial cancer in estrogen and oral contraceptive users were reviewed. The incidence of mammary malignancy in postmenopausal estrogen users (141.0:100,000) was lower than that of the untreated women, ie, nonhormone users (342.3:100,000) (P less than or equal to .01). The incidence of breast cancer in the estrogen-progestogen users (67.3:100,000) was significantly lower than that of the untreated women and than that expected from the Third National Cancer Survey (188.3:100,000) and the National Cancer Institute (NCI) data (229.2:100,000) (P less than or equal to .01). Oral contraceptives also decreased the risk of breast carcinoma, since the incidence in users (10.3:100,000) was significantly lower than expected in this age group according to both the Third National Cancer Survey (53.3:100,000) and the NCI data (57.3:100,000) (P less than or equal to .01). Unopposed estrogen replacement therapy increased the incidence of endometrial cancer to 410.8:100,000, but progestogen added to estrogen therapy significantly decreased this incidence to 68.1:100,000 (P less than or equal to .0001). The estrogen-progestogen users also had a significantly lower incidence of endometrial carcinoma than the untreated women (258.3:100,000) (P less than or equal to .005). Oral contraceptives, particularly the combination pill with estrogen and progestogen in each tablet, are protective against adenocarcinoma of the endometrium. The incidence of endometrial cancer apparently increased in premenopausal women during our study from 10.9:100,000 women in the first five years to 41.9:100,000 during the last two years as birth control pill use declined from 8,693 users in 1975 to 5,563 users during 1981, primarily in women over the age of 35.
由于威尔福德霍尔空军医疗中心接受雌激素治疗的女性子宫内膜癌发病率并未如其他人所报告的那样增加,因此于1975年开始了一项前瞻性研究。基于这个数据库,对使用雌激素和口服避孕药的女性中的乳腺癌和子宫内膜癌病例进行了回顾。绝经后使用雌激素的女性中乳腺恶性肿瘤的发病率(141.0:100,000)低于未接受治疗的女性,即非激素使用者(342.3:100,000)(P≤0.01)。使用雌激素 - 孕激素的女性中乳腺癌的发病率(67.3:100,000)显著低于未接受治疗的女性以及第三次全国癌症调查(188.3:100,000)和美国国立癌症研究所(NCI)数据(229.2:100,000)所预期的发病率(P≤0.01)。口服避孕药也降低了患乳腺癌的风险,因为使用者中的发病率(10.3:100,000)根据第三次全国癌症调查(53.3:100,000)和NCI数据(57.3:100,000)在该年龄组中均显著低于预期(P≤0.01)。单纯雌激素替代疗法将子宫内膜癌的发病率提高到410.8:100,000,但在雌激素治疗中添加孕激素可将该发病率显著降低至68.1:100,000(P≤0.0001)。使用雌激素 - 孕激素的女性子宫内膜癌的发病率也显著低于未接受治疗的女性(258.3:100,000)(P≤0.005)。口服避孕药,尤其是每片都含有雌激素和孕激素的复方避孕药,对子宫内膜腺癌有预防作用。在我们的研究中,绝经前女性子宫内膜癌的发病率明显上升,从最初五年的10.9:100,000女性升至最后两年的41.9:100,000,这期间避孕药的使用从1975年的8693名使用者降至1981年的5563名使用者,主要是35岁以上的女性。