Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort

IGHD 医学 队列 儿科 不利影响 身材矮小 背景(考古学) 特发性矮身高 内科学 生长激素缺乏 生长激素 激素 生物 古生物学
作者
Mohamad Maghnie,Michael B. Ranke,Mitchell E. Geffner,Elpis Vlachopapadopoulou,Lourdes Ibáñez,Martin Carlsson,Wayne S. Cutfield,Raoul Rooman,Roy Gomez,Michael Wajnrajch,Agnès Linglart,Renata Stawerska,Peter Clayton,Feyza Darendelıler,Anita C S Hokken-Koelega,Reiko Horikawa,Toshiaki Tanaka,Helmuth‐Günther Dörr,Kerstin Albertsson‐Wikland,Michel Polak,Adda Grimberg
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [The Endocrine Society]
卷期号:107 (12): 3287-3301 被引量:36
标识
DOI:10.1210/clinem/dgac517
摘要

The Kabi/Pfizer International Growth Database (KIGS) is a large, international database (1987-2012) of children treated with recombinant human growth hormone (rhGH) in real-world settings.This work aimed to evaluate the safety and efficacy of rhGH from the full KIGS cohort.Data were collected by investigators from children with growth disorders treated with rhGH (Genotropin [somatropin]; Pfizer). Safety was evaluated in all treated patients, and efficacy in those treated for 1 year or more. A subgroup included patients treated for 5 years or more (≥ 2 years prepubertal) who had reached near-adult height (NAH). Main outcomes included adverse events (AEs), serious AEs (SAEs), and height growth.The full KIGS cohort (N = 83 803 [58% male]) was treated for idiopathic GH deficiency (IGHD; 46.9%), organic GHD (10.0%), small for gestational age (SGA; 9.5%), Turner syndrome (TS; 9.2%), idiopathic short stature (ISS; 8.2%), and others (16.2%). Median rhGH treatment duration was 2.7 years and observation 3.1 years. SAEs occurred in 3.7% of patients and death in 0.4%. The most common SAEs were recurrence of craniopharyngioma (n = 151), neoplasm (n = 99), and cancer (n = 91); and scoliosis (n = 91). Median first-year delta height-SD score (SDS) (Prader) in prepubertal patients was 0.66 (IGHD), 0.55 (ISS), 0.58 (TS), and 0.71 (SGA). Median gains in NAH-SDS were 1.79 (IGHD), 1.37 (ISS), and 1.34 (SGA) for boys, and 2.07 (IGHD), 1.62 (ISS), 1.07 (TS), and 1.57 (SGA) for girls.Data from KIGS, the largest and longest running international database of rhGH-treated children, show that rhGH is safe and increases short-term height gain and adult height across GHD and non-GHD conditions.
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