Wells Michael, Sturdee David W, Barlow David H, Ulrich Lian G, O'Brien Karen, Campbell Michael J, Vessey Martin P, Bragg Anthony J
Academic Unit of Pathology, Section of Oncology and Pathology, Division of Genomic Medicine, University of Sheffield Medical School, Sheffield S10 2RX, UK.
BMJ. 2002 Aug 3;325(7358):239. doi: 10.1136/bmj.325.7358.239.
To determine effects of five years of treatment with an oral continuous combined regimen of 2 mg 17beta-oestradiol and 1 mg norethisterone acetate on endometrial histology in postmenopausal women.
Follow up study in postmenopausal women.
31 menopause clinics in the United Kingdom.
534 postmenopausal women, all with an intact uterus, who had completed nine months of treatment with oral continuous combined 2 mg 17beta-oestradiol and 1 mg norethisterone acetate agreed to take part in a long term follow up study. Women were assigned to different groups on the basis of the treatment status immediately before entering the original study: 360 women had taken sequential oestrogen-progestogen hormone replacement therapy, 164 had taken no hormone replacement therapy, and 10 had taken unopposed oestrogen therapy.
Endometrial aspiration specimens were taken before the women started the continuous combined regimen, after 9 and 24-36 months, and at the end of the five year treatment period or on withdrawal from the study.
Results of endometrial histology.
The duration of treatment with continuous combined hormone replacement therapy was 4.4 (range 1.1-5.9) years. Data on endometrial specimens were available for 526 women after nine months of treatment, 465 women after 24-36 months of treatment, and 398 women who completed the five years treatment (345 women) or were withdrawn between the two latter visits for biopsies (53 women). No cases of endometrial hyperplasia or malignancy were detected at biopsy; 69% of women had an endometrium classified as atrophic or unassessable on completion of the study or withdrawal from it. Before the continuous combined therapy was started, complex hyperplasia was detected in 21 women who had taken sequential hormone replacement therapy before the study and in one who had taken unopposed oestrogen. All of these women had normal results on histological examination of endometrial tissue after nine months of treatment with continuous combined hormone replacement therapy, and hyperplasia did not recur after up to five years of treatment.
Long term treatment (for up to five years) with continuous combined hormone replacement therapy containing oestradiol 2 mg and norethisterone 1 mg daily was associated with neither endometrial hyperplasia nor malignancy. In women who had complex hyperplasia during previous sequential or unopposed regimens, the endometrium returned to normal during treatment with continuous combined hormone replacement therapy. These findings provide reassurance about the long term safety of this continuous combined regimen in terms of the endometrium.
确定采用每日2毫克17β-雌二醇与1毫克醋酸炔诺酮口服连续联合方案治疗五年对绝经后妇女子宫内膜组织学的影响。
绝经后妇女随访研究。
英国31家更年期诊所。
534名绝经后妇女,均有完整子宫,已完成9个月每日2毫克17β-雌二醇与1毫克醋酸炔诺酮口服连续联合治疗,同意参加一项长期随访研究。根据进入原研究前的治疗状态将妇女分为不同组:360名妇女曾接受序贯雌激素-孕激素激素替代疗法,164名妇女未接受激素替代疗法,10名妇女曾接受单纯雌激素疗法。
在妇女开始连续联合方案治疗前、治疗9个月及24 - 36个月后、五年治疗期结束时或退出研究时采集子宫内膜抽吸标本。
子宫内膜组织学结果。
连续联合激素替代疗法的治疗时间为4.4(范围1.1 - 5.9)年。治疗9个月后有526名妇女的子宫内膜标本数据,治疗24 - 36个月后有465名妇女的数据,完成五年治疗的345名妇女及在最后两次访视活检之间退出的53名妇女共398名妇女有数据。活检未检测到子宫内膜增生或恶性病变;69%的妇女在研究结束或退出时子宫内膜分类为萎缩或无法评估。在开始连续联合治疗前,21名在研究前接受序贯激素替代疗法的妇女及1名接受单纯雌激素疗法的妇女检测到复杂性增生。所有这些妇女在连续联合激素替代疗法治疗9个月后子宫内膜组织学检查结果正常,治疗长达五年后增生未复发。
每日含2毫克雌二醇和1毫克醋酸炔诺酮的连续联合激素替代疗法长期治疗(长达五年)既未导致子宫内膜增生也未引发恶性病变。在之前序贯或单纯疗法期间有复杂性增生的妇女中,连续联合激素替代疗法治疗期间子宫内膜恢复正常。这些发现为该连续联合方案在子宫内膜方面的长期安全性提供了保障。