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重组人生长激素联合重组人胰岛素样生长因子-1治疗胰岛素样生长因子-1水平低且生长激素充足的矮小儿童:一项随机、多中心、开放标签、平行组、活性治疗对照试验的结果

Recombinant human growth hormone plus recombinant human insulin-like growth factor-1 coadministration therapy in short children with low insulin-like growth factor-1 and growth hormone sufficiency: results from a randomized, multicenter, open-label, parallel-group, active treatment-controlled trial.

作者信息

Backeljauw Philippe F, Miller Bradley S, Dutailly Pascale, Houchard Aude, Lawson Elizabeth, Hale Daniel E, Reiner Barry, Sperling Mark A

机构信息

Division of Pediatric Endocrinology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.

出版信息

Horm Res Paediatr. 2015;83(4):268-79. doi: 10.1159/000371799. Epub 2015 Mar 6.

DOI:10.1159/000371799
PMID:25765099
Abstract

BACKGROUND/AIMS: Growth hormone (GH) and insulin-like growth factor-1 (IGF-1) both contribute to growth. To determine if recombinant human (rh)GH + rhIGF-1 therapy is more effective than rhGH alone to treat short stature, we assessed the efficacy and safety of coadministered rhGH + rhIGF-1 in short children with GH sufficiency and low IGF-1.

METHODS

In a 3-year, randomized, multicenter, open-label trial, patients with height SD score ≤-2.0 and IGF-1 SD score ≤-1.0 for age and sex, and with stimulated GH ≥10 ng/ml for age and sex, were randomized to receive (all doses in µg/kg/day): 45 rhGH alone (group A), 45 rhGH + 50 rhIGF-1 (group B), 45 rhGH + 100 rhIGF-1 (group C) or 45 rhGH + 150 rhIGF-1 (group D). Height velocity (HV) and Δ height SD score were measured.

RESULTS

The first-year HV (modified intention-to-treat population) was 9.3 ± 1.7 cm/year (group A), 10.1 ± 1.3 cm/year (group B), 9.7 ± 2.5 cm/year (group C) and 11.2 ± 2.1 cm/year (group D) (p = 0.001 for groups A vs. D). This effect was sustained, resulting in a height SD score improvement during the second and third years. Most treatment-emergent adverse events were mild and transient.

CONCLUSION

In children with short stature, GH sufficiency and low IGF-1, coadministration of rhGH/rhIGF-1 (45/150 µg/kg) significantly accelerated linear growth compared with rhGH alone, with a safety profile similar to the individual monotherapies.

摘要

背景/目的:生长激素(GH)和胰岛素样生长因子-1(IGF-1)均对生长有促进作用。为确定重组人生长激素(rhGH)联合重组人胰岛素样生长因子-1(rhIGF-1)治疗对矮小症的疗效是否优于单独使用rhGH,我们评估了联合使用rhGH和rhIGF-1治疗生长激素充足但IGF-1水平低的矮小儿童的疗效和安全性。

方法

在一项为期3年的随机、多中心、开放标签试验中,身高标准差评分(SD评分)≤-2.0且IGF-1 SD评分≤-1.0(根据年龄和性别),且生长激素刺激试验≥10 ng/ml(根据年龄和性别)的患者被随机分组接受(所有剂量均为μg/kg/天):单独使用45 μg rhGH(A组)、45 μg rhGH + 50 μg rhIGF-1(B组)、45 μg rhGH + 100 μg rhIGF-1(C组)或45 μg rhGH + 150 μg rhIGF-1(D组)。测量身高生长速度(HV)和身高标准差评分变化(Δ身高SD评分)。

结果

第一年的身高生长速度(改良意向性治疗人群)分别为:A组9.3±1.7 cm/年、B组10.1±1.3 cm/年、C组9.7±2.5 cm/年、D组11.2±2.1 cm/年(A组与D组相比,p = 0.001)。这种效果得以持续,在第二年和第三年身高标准差评分有所改善。大多数治疗中出现的不良事件为轻度且短暂。

结论

在生长激素充足但IGF-1水平低的矮小儿童中,与单独使用rhGH相比,联合使用rhGH/rhIGF-1(45/150 μg/kg)显著加速了线性生长,其安全性与单独使用单一疗法相似。

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