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奥司米芬对女性生殖和泌尿系统的影响:从临床前模型到临床证据的转化

Effects of ospemifene on the female reproductive and urinary tracts: translation from preclinical models into clinical evidence.

作者信息

Archer David F, Carr Bruce R, Pinkerton JoAnn V, Taylor Hugh S, Constantine Ginger D

机构信息

From the 1Eastern Virginia Medical School, Norfolk, VA; 2University of Texas Southwestern Medical Center, Dallas, TX; 3University of Virginia, Charlottesville, VA; 4Yale School of Medicine, New Haven, CT; and 5Endorheum Consultants, Malvern, PA.

出版信息

Menopause. 2015 Jul;22(7):786-96. doi: 10.1097/GME.0000000000000365.

Abstract

OBJECTIVE

Treatment of menopausal symptoms by compounds with tissue-selective estrogen agonist/antagonist effects, often called selective estrogen receptor modulators, has been researched as an alternative to the use of estrogen therapy. These structurally diverse molecules elicit tissue-dependent responses in hormone-responsive tissues and organs, exhibiting variations in estrogenic activity in preclinical models of postmenopausal reproductive tissues that may improve postmenopausal women's health (eg, prevention and treatment of breast cancer, osteoporosis, and vulvar and vaginal atrophy).

METHODS

This literature review investigates whether preclinical data predicted the clinical effects of ospemifene on female reproductive and urinary tract tissues and compares these findings with the specific vaginal effects of other estrogen receptor agonists/antagonists (tamoxifen, raloxifene, and bazedoxifene) in preclinical and clinical studies. Lasofoxifene, although not currently available, is included because of its unique effects on vaginal tissue.

RESULTS

The response of endometrial and vaginal tissues to estrogen receptor agonists/antagonists can be differentiated using transvaginal ultrasound, endometrial histopathology, cytologic examination of vaginal smears, assessment of physical changes in the vagina, and relief of symptoms associated with vulvar and vaginal atrophy (such as dyspareunia).

CONCLUSIONS

Available evidence indicates that ospemifene has unique effects on tissue, leading to a favorable long-term profile for the relief of vulvar and vaginal atrophy compared with other estrogen receptor agonists/antagonists (eg, tamoxifen, raloxifene, and bazedoxifene) with no short-term concerns about endometrial safety (based on endometrial hyperplasia, carcinoma, endometrial spotting, and endometrial bleeding).

摘要

目的

具有组织选择性雌激素激动剂/拮抗剂作用的化合物(常被称为选择性雌激素受体调节剂)用于治疗更年期症状,已作为雌激素疗法的替代方法进行了研究。这些结构多样的分子在激素反应性组织和器官中引发组织依赖性反应,在绝经后生殖组织的临床前模型中表现出雌激素活性的差异,这可能改善绝经后女性的健康状况(例如预防和治疗乳腺癌、骨质疏松症以及外阴和阴道萎缩)。

方法

这篇文献综述调查临床前数据是否能预测奥司米芬对女性生殖和泌尿道组织的临床效果,并将这些结果与其他雌激素受体激动剂/拮抗剂(他莫昔芬、雷洛昔芬和巴多昔芬)在临床前和临床研究中的特定阴道效果进行比较。尽管拉索昔芬目前尚未上市,但因其对阴道组织有独特作用而被纳入。

结果

可通过经阴道超声、子宫内膜组织病理学、阴道涂片细胞学检查、评估阴道的物理变化以及缓解与外阴和阴道萎缩相关的症状(如性交困难)来区分子宫内膜和阴道组织对雌激素受体激动剂/拮抗剂的反应。

结论

现有证据表明,与其他雌激素受体激动剂/拮抗剂(如他莫昔芬、雷洛昔芬和巴多昔芬)相比,奥司米芬对组织有独特作用,在缓解外阴和阴道萎缩方面具有良好的长期效果,且不存在短期的子宫内膜安全性问题(基于子宫内膜增生、癌、子宫内膜点状出血和子宫内膜出血)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1e8/4481022/fd53463563d1/gme-22-786-g003.jpg

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