Wong J M, Forrest K A, Snabes S Z, Zhao S Z, Gersh G E, Kennedy S H
Global Outcomes Research, Pharmacia Corporation, Skokie, IL 60077, USA.
Hum Reprod Update. 2001 Jan-Feb;7(1):92-101. doi: 10.1093/humupd/7.1.92.
A systematic review identified nine randomized, controlled trials (both published and unpublished) which assessed the efficacy of nafarelin during IVF compared with other gonadotrophin-releasing hormone (GnRH) agonists. The trials included 1,014 women (nafarelin n = 597) in protocols employing three different dosage regimens, long and short stimulation protocols, and three comparative GnRH agonists (buserelin n = 348; triptorelin n = 14, and leuprolide n = 55). The meta-analysis of the data showed that pregnancy rates per embryo transfer with nafarelin were equivalent to those obtained with other GnRH agonists. Nafarelin and other agonists were also comparable in terms of several intermediate IVF outcomes, including fertilization rates, number of oocytes retrieved, peak oestradiol concentrations, and cycle cancellations. Women treated with nafarelin required fewer ampoules of human menopausal gonadotrophin (HMG)/FSH for ovarian stimulation and fewer days of stimulation. Safety results from both the meta-analysis and a qualitative analysis of 12 additional reports suggested that adverse effects were within the accepted tolerance range; the most frequent adverse effects were hypo-oestrogenic symptoms. In conclusion, the overall efficacy of nafarelin was equivalent to that of other GnRH agonists. The possibility that the reduced gonadotrophin requirements in women taking nafarelin will translate into cost savings per IVF treatment cycle requires further study.
一项系统评价纳入了9项随机对照试验(包括已发表和未发表的),这些试验评估了那法瑞林在体外受精(IVF)过程中与其他促性腺激素释放激素(GnRH)激动剂相比的疗效。这些试验纳入了1014名女性(那法瑞林组n = 597),采用了三种不同的给药方案、长方案和短方案刺激方案,以及三种对照GnRH激动剂(布舍瑞林组n = 348;曲普瑞林组n = 14,亮丙瑞林组n = 55)。数据的荟萃分析表明,那法瑞林组每次胚胎移植的妊娠率与其他GnRH激动剂组相当。那法瑞林和其他激动剂在几个IVF中间结局方面也具有可比性,包括受精率、回收的卵母细胞数量、雌二醇峰值浓度和周期取消率。接受那法瑞林治疗的女性在卵巢刺激时需要的人绝经期促性腺激素(HMG)/FSH安瓿较少,刺激天数也较少。荟萃分析和对另外12份报告的定性分析的安全性结果表明,不良反应在可接受的耐受范围内;最常见的不良反应是低雌激素症状。总之,那法瑞林的总体疗效与其他GnRH激动剂相当。服用那法瑞林的女性促性腺激素需求减少是否会转化为每个IVF治疗周期的成本节约,这一可能性需要进一步研究。