Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, Ohio.
Arthritis Rheumatol. 2015 May;67(5):1377-85. doi: 10.1002/art.39024.
To determine the dose of triptorelin that is sufficient to maintain complete ovarian suppression in female patients with childhood-onset systemic lupus erythematosus (SLE) who require cyclophosphamide therapy, to determine the length of time needed to achieve ovarian suppression after initiation of triptorelin treatment, and to investigate the safety of triptorelin.
In this randomized, double-blind, placebo-controlled, dose-escalation study, female patients ages <21 years were randomized 4:1 to receive triptorelin (n = 25) or placebo (n = 6). The starting doses of triptorelin were 25, 50, 75, and 100 μg/kg, and the dose was escalated until complete ovarian suppression was maintained. The primary outcome was the weight-adjusted dose of triptorelin that provided complete ovarian suppression in at least 90% of the patients, as determined by gonadotropin-releasing hormone agonist stimulation testing. The secondary outcome was the period of time required to achieve ovarian suppression, as measured by unstimulated follicle-stimulating hormone and luteinizing hormone levels after the initiation of triptorelin treatment.
Treatment with triptorelin at a weight-adjusted dose of 120 μg/kg body weight provided sustained complete ovarian suppression in 90% of the patients. After administration of the initial dose of triptorelin, 22 days were required to achieve complete ovarian suppression. The rates of adverse events (AEs) and serious adverse events (SAEs) per 100 patient-months of followup were not higher in the triptorelin group compared with the placebo group (for AEs, 189 versus 362; for SAEs, 2.1 versus 8.5).
High doses of triptorelin are needed to achieve and maintain complete ovarian suppression, but such doses appear to be well tolerated in adolescent female patients with childhood-onset SLE. Our data suggest that a lag time of 22 days after initiation of triptorelin treatment is required before cyclophosphamide therapy is started or continued.
确定三苯氧胺的剂量,以维持需要环磷酰胺治疗的儿童期起病系统性红斑狼疮(SLE)女性患者的完全卵巢抑制,确定起始三苯氧胺治疗后达到卵巢抑制所需的时间,并研究三苯氧胺的安全性。
在这项随机、双盲、安慰剂对照、剂量递增研究中,年龄<21 岁的女性患者以 4:1 的比例随机分为三苯氧胺(n=25)或安慰剂(n=6)组。三苯氧胺的起始剂量为 25、50、75 和 100μg/kg,剂量递增至至少 90%的患者维持完全卵巢抑制。主要结局是通过促性腺激素释放激素激动剂刺激试验确定的提供至少 90%患者完全卵巢抑制的三苯氧胺体重调整剂量。次要结局是从开始三苯氧胺治疗后通过未刺激的卵泡刺激素和黄体生成素水平达到卵巢抑制所需的时间。
三苯氧胺的体重调整剂量为 120μg/kg 体重时,可提供持续的完全卵巢抑制,90%的患者达到此效果。给予初始三苯氧胺剂量后,需要 22 天才能达到完全卵巢抑制。与安慰剂组相比,三苯氧胺组每 100 患者-月的不良事件(AE)和严重不良事件(SAE)发生率(AE,189 比 362;SAE,2.1 比 8.5)并未更高。
需要高剂量的三苯氧胺来实现和维持完全卵巢抑制,但在儿童期起病 SLE 的青少年女性患者中,这种剂量似乎可以耐受。我们的数据表明,在开始或继续环磷酰胺治疗之前,需要在起始三苯氧胺治疗后 22 天的延迟时间。