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每周一次索马帕西坦用于青春期前儿童生长激素缺乏的替代治疗:一项随机对照试验的系统评价和荟萃分析

Once-Weekly Somapacitan as an Alternative Management of Growth Hormone Deficiency in Prepubertal Children: A Systematic Review and Meta-Analysis of Randomized Controlled Trial.

作者信息

Tsurayya Ghina, Nazhifah Cut Alifiya, Pirwanja Muhammad Rahmat, Zulfa Putri Oktaviani, Tatroman Muhammad Raihan Ramadhan, Fakri Fajar, Iqhrammullah Muhammad

机构信息

Medical Research Unit, School of Medicine, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia.

Department of Pharmacy, Faculty of Mathematics and Natural Sciences, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia.

出版信息

Children (Basel). 2024 Feb 9;11(2):227. doi: 10.3390/children11020227.

Abstract

Growth hormone treatment has effectively restored normal growth in children with growth hormone deficiency (GHD); however, it poses challenges in compliance with a daily growth hormone injection regimen, leading to low adherence and persistence rates. Once-weekly Somapacitan is a potential alternative for treating children with GHD. This study aimed to evaluate the efficacy, safety, and adherence of once-weekly subcutaneous Somapacitan compared to daily growth hormone injection in prepubertal children with GHD. A search for the published records was carried out on 17 October 2023 utilizing the searching feature available on PubMed, Embase, and Scopus. Primary study outcomes included (1) efficacy, measured by height velocity (HV), standard deviation score (SDs), height SDs, insulin-like growth factor-SDs (IGF-I SDs), and bone age vs. chronological age ratio (BA vs. CA); (2) safety, assessed through adverse events and injection site reactions; and (3) adherence, determined by the percentage of the sample completing treatments. Secondary outcomes evaluated disease burden scores, divided into three subgroup domains: emotional well-being, physical functional, and social well-being scores. We retrieved 6 studies that were eligible for the systematic review (417 versus 186 for intervention and control, respectively). Only 2 of the total included studies were eligible for pooled analysis (175 versus 82 for intervention and control, respectively). The efficacy profile of Somapacitan was similar to daily growth hormones, indicated by HV (mean difference (MD = 0.04; = 0.96), HV SDs (MD = -0.71; = 0.09), height SDs (MD = 0.11; = 0.69), IGF-I SDs (MD = 0.06; = 0.70), and CA vs. BA (MD = 0.67; = 0.70)), demonstrated similar and non-inferior outcomes. Treatment adherence is 3 times higher in the Somapacitan group as compared to control (OR = 3.02; = 0.03) with adherence rates reaching 95% and 88% for Somapacitan and Norditropin, respectively. The disease burden measurement is similar in Somapacitan and daily growth hormones (MD = -0.62; = 0.83), as indicated by the Growth Hormone Deficiency-Child Impact Measure. In almost all outcomes, the level of confidence is strong. The confidence level in the data is generally strong, but for CA vs. BA and the subgroup of severe adverse events with heterogeneity >50%, the confidence level is moderate. Although the efficacy and safety profiles of Somapacitan were found to be similar to those of daily growth hormones, a reduced frequency of once-weekly Somapacitan injections led to increased adherence. PROSPERO registration: CRD42023473209.

摘要

生长激素治疗已有效恢复了生长激素缺乏症(GHD)儿童的正常生长;然而,每日注射生长激素的治疗方案在依从性方面存在挑战,导致依从率和持续率较低。每周一次的索马普西坦是治疗GHD儿童的一种潜在替代药物。本研究旨在评估与每日注射生长激素相比,每周一次皮下注射索马普西坦治疗青春期前GHD儿童的疗效、安全性和依从性。2023年10月17日,利用PubMed、Embase和Scopus上的搜索功能对已发表的记录进行了检索。主要研究结果包括:(1)疗效,通过身高增长速度(HV)、标准差评分(SDs)、身高标准差、胰岛素样生长因子标准差(IGF-I SDs)以及骨龄与实际年龄之比(BA与CA)来衡量;(2)安全性,通过不良事件和注射部位反应进行评估;(3)依从性,由完成治疗的样本百分比确定。次要结果评估疾病负担评分,分为三个亚组领域:情绪健康、身体功能和社会健康评分。我们检索到6项符合系统评价条件的研究(干预组和对照组分别为417例和186例)。纳入的研究中只有2项符合荟萃分析条件(干预组和对照组分别为175例和82例)。索马普西坦的疗效与每日生长激素相似,如HV(平均差(MD = 0.04;P = 0.96))、HV SDs(MD = -0.71;P = 0.09)、身高SDs(MD = 0.11;P = 0.69)、IGF-I SDs(MD = 0.06;P = 0.70)以及CA与BA(MD = 0.67;P = 0.70)所示,显示出相似且非劣效的结果。索马普西坦组的治疗依从性比对照组高3倍(OR = 3.02;P = 0.03),索马普西坦和诺德生长激素的依从率分别达到95%和88%。生长激素缺乏症儿童影响测量结果表明,索马普西坦和每日生长激素的疾病负担测量结果相似(MD = -0.62;P = 0.83)。在几乎所有结果中,置信水平都很高。数据的置信水平总体上较高,但对于CA与BA以及异质性>50%的严重不良事件亚组,置信水平为中等。虽然发现索马普西坦的疗效和安全性与每日生长激素相似,但每周一次的索马普西坦注射频率降低导致依从性提高。PROSPERO注册号:CRD42023473209。

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