Benabbad Imane, Rosilio Myriam, Tauber Maité, Paris Emmanuel, Paulsen Anne, Berggren Lovisa, Patel Hiren, Carel Jean-Claude
Endocrinology and Diabetes UnitEli Lilly, Neuilly-sur-Seine, France.
Department EndocrineBone Diseases, Genetics, Obesity, and Gynecology Unit, Children's Hospital, University Hospital, Toulouse, France.
Endocr Connect. 2018 May;7(5):708-718. doi: 10.1530/EC-18-0137. Epub 2018 Apr 18.
There is a scarcity of data from randomised controlled trials on the association of growth hormone (GH) with gonadotrophin-releasing hormone agonists in idiopathic short stature (ISS), although this off-label use is common. We aimed to test whether delaying pubertal progression could increase near-adult height (NAH) in GH-treated patients with ISS.
Patients with ISS at puberty onset were randomised to GH with leuprorelin (combination, = 46) or GH alone ( = 45). NAH standard deviation score (SDS) was the primary outcome measure. The French regulatory authority requested premature discontinuation of study treatments after approximately 2.4 years; patients from France were followed for safety.
Mean (s.d.) baseline height SDS was -2.5 (0.5) in both groups, increasing at 2 years to -2.3 (0.6) with combination and -1.8 (0.7) with GH alone. NAH SDS was -1.8 (0.5) with combination ( = 19) and -1.9 (0.8) with GH alone ( = 16). Treatment-emergent adverse events and bone fractures occurred more frequently with combination than GH alone.
Due to premature discontinuation of treatments, statistical comparison of NAH SDS between the two cohorts was not possible. During the first 2-3 years of treatment, patients treated with the combination grew more slowly than those receiving GH alone. However, mean NAH SDS was similar in the two groups. No new GH-related safety concerns were revealed. A potentially deleterious effect of combined treatment on bone fracture incidence was identified.
关于生长激素(GH)与促性腺激素释放激素激动剂联合用于特发性矮小症(ISS)的随机对照试验数据稀缺,尽管这种超说明书用药很常见。我们旨在测试延迟青春期发育是否能增加接受GH治疗的ISS患者的近成人身高(NAH)。
青春期开始时的ISS患者被随机分为接受GH联合亮丙瑞林治疗组(联合组,n = 46)或单独接受GH治疗组(n = 45)。NAH标准差评分(SDS)是主要结局指标。法国监管机构要求在约2.4年后提前终止研究治疗;对来自法国的患者进行安全性随访。
两组的平均(标准差)基线身高SDS均为-2.5(0.5),联合组在2年时增加到-2.3(0.6),单独使用GH组增加到-1.8(0.7)。联合组的NAH SDS为-1.8(0.5)(n = 19),单独使用GH组为-1.9(0.8)(n = 16)。联合治疗出现的不良事件和骨折比单独使用GH更频繁。
由于治疗提前终止,无法对两组队列的NAH SDS进行统计学比较。在治疗的前2至3年,联合治疗的患者比单独接受GH治疗的患者生长更缓慢。然而,两组的平均NAH SDS相似。未发现新的与GH相关的安全问题。确定了联合治疗对骨折发生率有潜在有害影响。