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首页> 外文期刊>International Journal of Women s Health >Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program
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Safety and tolerability of dienogest in endometriosis: pooled analysis from the European clinical study program

机译:子宫内膜异位症中烯诺孕的安全性和耐受性:欧洲临床研究计划的汇总分析

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Background: In four randomized, controlled, European trials, dienogest 2?mg once daily demonstrated significant efficacy for lesion reduction and reduction in pain intensity in endometriosis. We describe a pooled analysis of the safety and tolerability data?from these trials to confirm and further characterize the safety profile of dienogest in the treatment of endometriosis.Methods: All 332 women treated with dienogest 2?mg who participated in the four clinical trials were included in the pooled analyses for safety assessments, including adverse events, laboratory tests, vital signs, body weight, and bleeding patterns. Safety variables were analyzed using descriptive statistics.Results: Pooled analyses of this large patient population confirmed that dienogest?2?mg is well tolerated, with a favorable safety profile extending over a period up to 65?weeks in women with endometriosis. The most common adverse drug reactions were headache, breast discomfort, depressed mood, and acne, each occurring in <10% of women. All these adverse events were generally of mild-to-moderate intensity and associated with low discontinuation rates. The bleeding pattern associated with dienogest 2?mg was well tolerated, and only two women (0.6%) reported bleeding events as the primary reason for premature discontinuation. Laboratory and vital sign assessments indicated no safety concerns for dienogest. Estradiol levels were maintained within the low-physiological range, in support of previous evidence indicating that dienogest?2?mg demonstrates therapeutic efficacy without inducing estradiol?deficiency.Conclusion: In this pooled analysis of 332 women with endometriosis, dienogest was well tolerated with a favorable safety profile extending over a period of up to 65?weeks. There is a paucity of randomized trial evidence to support the use of many treatments in endometriosis. These pooled analyses from four clinical trials of dienogest?2?mg represent a contribution to evidence-based medicine in endometriosis, providing outcomes of potential relevance to daily practice.
机译:背景:在四项随机,对照,欧洲试验中,每日一次2毫克地诺孕酮显示出明显的功效,可减少病灶并减轻子宫内膜异位症的疼痛强度。我们对这些试验的安全性和耐受性数据进行了汇总分析,以确认并进一步表征去死孕激素在治疗子宫内膜异位症中的安全性。方法:参加这四项临床试验的全部332名接受去死孕激素2 mg治疗的妇女均包括在用于安全评估的汇总分析中,包括不良事件,实验室检查,生命体征,体重和出血模式。结果:对大量患者进行的汇总分析证实,对内诺非特2毫克的耐受性良好,子宫内膜异位症患者的安全性良好,有效期长达65周。最常见的药物不良反应是头痛,乳房不适,情绪低落和痤疮,每发生在10%的女性中。所有这些不良事件通常为轻至中度,并伴有低停药率。耐受性良好,与2 mg每日一次止痛药相关的出血模式耐受良好,只有两名女性(0.6%)报告出血事件为过早停药的主要原因。实验室和生命体征评估表明,没有任何安全隐患。雌二醇水平维持在较低的生理范围内,以支持先前的证据表明,地诺孕酮2mg在不引起雌二醇缺乏的情况下显示出治疗功效。结论:在对332例子宫内膜异位症妇女的综合分析中,对地诺孕酮的耐受性良好良好的安全性长达65周。很少有随机试验证据支持在子宫内膜异位症中使用多种治疗方法。这些来自4例地诺孕酮2 mg临床试验的汇总分析代表了对子宫内膜异位症循证医学的贡献,并提供了与日常实践潜在相关的结果。

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