Department of Pathology, McGill University Health Center, Montreal, Canada.
University of Manitoba, Winnipeg, Canada.
Menopause. 2023 Aug 1;30(8):855-866. doi: 10.1097/GME.0000000000002211. Epub 2023 Jun 27.
Ospemifene is a novel selective estrogen receptor modulator developed for the treatment of moderate to severe postmenopausal vulvovaginal atrophy (VVA).
The aim of the study is to perform a systematic literature review (SLR) and network meta-analysis (NMA) to assess the efficacy and safety of ospemifene compared with other therapies used in the treatment of VVA in North America and Europe.
Electronic database searches were conducted in November 2021 in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Randomized or nonrandomized controlled trials targeting postmenopausal women with moderate to severe dyspareunia and/or vaginal dryness and involving ospemifene or at least one VVA local treatment were considered. Efficacy data included changes from baseline in superficial and parabasal cells, vaginal pH, and the most bothersome symptom of vaginal dryness or dyspareunia, as required for regulatory approval. Endometrial outcomes were endometrial thickness and histologic classifications, including endometrial polyp, hyperplasia, and cancer. For efficacy and safety outcomes, a Bayesian NMA was performed. Endometrial outcomes were compared in descriptive analyses.
A total of 44 controlled trials met the eligibility criteria ( N = 12,637 participants). Network meta-analysis results showed that ospemifene was not statistically different from other active therapies in most efficacy and safety results. For all treatments, including ospemifene, the posttreatment endometrial thickness values (up to 52 wk of treatment) were under the recognized clinical threshold value of 4 mm for significant risk of endometrial pathology. Specifically, for women treated with ospemifene, endometrial thickness ranged between 2.1 and 2.3 mm at baseline and 2.5 and 3.2 mm after treatment. No cases of endometrial carcinoma or hyperplasia were observed in ospemifene trials, nor polyps with atypical hyperplasia or cancer after up to 52 weeks of treatment.
Ospemifene is an efficacious, well-tolerated, and safe therapeutic option for postmenopausal women with moderate to severe symptoms of VVA. Efficacy and safety outcomes with ospemifene are similar to other VVA therapies in North America and Europe.
奥昔布芬是一种新型选择性雌激素受体调节剂,用于治疗中重度绝经后阴道萎缩(VVA)。
本研究旨在进行系统文献综述(SLR)和网络荟萃分析(NMA),评估奥昔布芬与北美和欧洲用于治疗 VVA 的其他疗法相比的疗效和安全性。
根据系统评价和荟萃分析的首选报告项目指南,于 2021 年 11 月进行了电子数据库搜索。纳入针对中重度性交痛和/或阴道干燥的绝经后妇女的随机或非随机对照试验,涉及奥昔布芬或至少一种 VVA 局部治疗。疗效数据包括监管批准所需的从基线变化的浅层和副基底层细胞、阴道 pH 值以及阴道干燥或性交痛的最困扰症状。子宫内膜结局包括子宫内膜厚度和组织学分类,包括子宫内膜息肉、增生和癌症。对于疗效和安全性结果,进行了贝叶斯 NMA。在描述性分析中比较了子宫内膜结局。
共有 44 项符合入选标准的对照试验(N=12637 名参与者)。网络荟萃分析结果表明,奥昔布芬在大多数疗效和安全性结果上与其他活性治疗药物无统计学差异。对于所有治疗方法,包括奥昔布芬,治疗后子宫内膜厚度值(长达 52 周治疗)低于公认的 4 毫米临床阈值,提示存在显著的子宫内膜病理风险。具体而言,接受奥昔布芬治疗的女性在基线时子宫内膜厚度为 2.1-2.3 毫米,治疗后为 2.5-3.2 毫米。奥昔布芬试验中未观察到子宫内膜癌或增生病例,也未观察到治疗长达 52 周后息肉伴非典型增生或癌症。
奥昔布芬是一种治疗中重度 VVA 绝经后妇女的有效、耐受良好且安全的治疗选择。奥昔布芬在北美和欧洲的疗效和安全性结果与其他 VVA 治疗药物相似。