Investigation of the 12-month efficacy and safety of low-dose mifepristone in the treatment of painful adenomyosis

IF 0.7 4区 医学 Q4 OBSTETRICS & GYNECOLOGY Reproductive and Developmental Medicine Pub Date : 2022-07-13 DOI:10.1097/RD9.0000000000000031
Shu-yi Chen, Mengchao Zhao, Wen-Ting Sun, Li-bo Zhu, Xin-Mei Zhang
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Abstract

Objective: To study the 12-month effects and possible mechanisms of low-dose mifepristone in the treatment of adenomyosis. Methods: Patients included in this retrospective study had painful adenomyosis and previously received 5 mg mifepristone daily (group A, n = 45) or 5 mg mifepristone daily with a poor-effect levonorgestrel-releasing intrauterine device (group B, n = 13) for 12 months. Uterine size, serum CA125 levels, estradiol levels, Visual Analogue Scale (VAS) score, endometrial thickness, and hemoglobin levels were compared before and after treatment and investigated again at 3 to 6 months after drug withdrawal. Another 8 patients with adenomyosis (group C, n = 8) who underwent surgery for severe dysmenorrhea during the same period were only used as a control group for immunohistochemical research. Endometrial biopsy results and expression of nerve growth factor (NGF), cyclooxygenase-2 (COX-2), and nuclear-associated antigen Ki-67 (Ki-67) in endometrial tissues and adenomyotic lesions were also analyzed. Results: The VAS scores in both experimental groups at all time points during treatment and follow-up were significantly lower (P <0.001) than those before treatment. The uterine size was significantly reduced, and endometrial thickness was distinctly thicker after 12 months of treatment than that before treatment in group A receiving 5 mg/d mifepristone. The immunohistochemical expression of NGF and COX-2 decreased in both eutopic and ectopic endometrium after treatment, whereas that of Ki-67 slightly increased in eutopic endometrium after treatment and rapidly recovered to the baseline value after stopping mifepristone. There were no signs of hyperplasia, atypical hyperplasia, or malignancy in the endometrial biopsies. Conclusions: The results suggested that a daily dose of 5 mg mifepristone for 12 months down-regulated the expression of NGF and COX-2 and was effective in treating painful adenomyosis with few side effects.
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低剂量米非司酮治疗疼痛性脑出血12个月疗效及安全性观察
目的:探讨小剂量米非司酮治疗子宫腺肌病12个月的疗效及可能机制。方法:纳入这项回顾性研究的患者有疼痛的子宫腺肌症,之前接受了5 米非司酮mg每日(A组,n = 45)或5 mg米非司酮每日联合左炔诺孕酮缓释宫内节育器效果不佳(B组,n = 13) 为期12个月。比较治疗前后子宫大小、血清CA125水平、雌二醇水平、视觉模拟量表(VAS)评分、子宫内膜厚度和血红蛋白水平,并在停药后3-6个月再次进行研究。另有8例腺肌症患者(C组 = 8) 同期接受严重痛经手术的患者仅作为对照组进行免疫组化研究。还分析了子宫内膜活检结果以及神经生长因子(NGF)、环氧合酶-2(COX-2)和核相关抗原Ki-67(Ki-67)在子宫内膜组织和子宫腺肌病病变中的表达。结果:两个实验组在治疗和随访的各个时间点VAS评分均显著低于对照组(P <0.001)。治疗12个月后,接受5 mg/d米非司酮。NGF和COX-2在治疗后在位和异位子宫内膜的免疫组织化学表达均下降,而Ki-67在治疗后在在位子宫内膜的表达略有增加,并在停止米非司酮后迅速恢复到基线值。子宫内膜活检中没有增生、不典型增生或恶性肿瘤的迹象。结论:结果表明,每天5 mg米非司酮12个月可下调NGF和COX-2的表达,对治疗疼痛性子宫腺肌病有效,副作用少。
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来源期刊
Reproductive and Developmental Medicine
Reproductive and Developmental Medicine OBSTETRICS & GYNECOLOGY-
CiteScore
1.60
自引率
12.50%
发文量
384
审稿时长
23 weeks
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