Eli Lilly and Company, Windlesham, Surrey, United Kingdom.
Eli Lilly and Company, Indianapolis, Indiana.
J Clin Endocrinol Metab. 2019 Feb 1;104(2):379-389. doi: 10.1210/jc.2018-01189.
Safety concerns have been raised regarding premature mortality, diabetes, neoplasia, and cerebrovascular disease in association with GH therapy.
To assess incidence of key safety outcomes.
Prospective, multinational, observational study (1999 to 2015).
A total of 22,311 GH-treated children from 827 investigative sites in 30 countries.
Children with growth disorders.
GH treatment.
Standardized mortality ratio (SMR) and standardized incidence ratio (SIR) with 95% CIs for mortality, diabetes, and primary cancer using general population registries.
Predominant short stature diagnoses were GH deficiency (63%), idiopathic short stature (13%), and Turner syndrome (8%), with mean ± SD follow-up of 4.2 ± 3.2 years (∼92,000 person-years [PY]). Forty-two deaths occurred in patients with follow-up, with an SMR (95% CI) of 0.61 (0.44, 0.82); the SMR was elevated for patients with cancer-related organic GH deficiency [5.87 (3.21, 9.85)]. Based on 18 cases, type 2 diabetes mellitus (T2DM) risk was elevated [SIR: 3.77 (2.24, 5.96)], but 72% had risk factors. In patients without cancer history, 14 primary cancers were observed [SIR: 0.71 (0.39, 1.20)]. Second neoplasms occurred in 31 of 622 cancer survivors [5.0%; 10.7 (7.5, 15.2) cases/1000 PY] and intracranial tumor recurrences in 67 of 823 tumor survivors [8.1%; 16.9 (13.3, 21.5) cases/1000 PY]. All three hemorrhagic stroke cases had risk factors.
GeNeSIS (Genetics and Neuroendocrinology of Short Stature International Study) data support the favorable safety profile of pediatric GH treatment. Overall risk of death or primary cancer was not elevated in GH-treated children, and no hemorrhagic strokes occurred in patients without risk factors. T2DM incidence was elevated compared with the general population, but most cases had diabetes risk factors.
生长激素(GH)治疗与过早死亡、糖尿病、肿瘤和脑血管疾病有关,因此引发了安全性担忧。
评估关键安全性结局的发生率。
前瞻性、多国、观察性研究(1999 年至 2015 年)。
来自 30 个国家 827 个研究点的 22311 名接受 GH 治疗的儿童。
生长障碍患儿。
GH 治疗。
使用一般人群登记处计算死亡率、糖尿病和原发性癌症的标准化死亡率比(SMR)和标准化发病比(SIR),并计算 95%可信区间。
主要矮小症诊断为 GH 缺乏症(63%)、特发性矮小症(13%)和 Turner 综合征(8%),平均随访时间为 4.2±3.2 年(约 92000 人年)。42 例患者在随访期间死亡,SMR(95%CI)为 0.61(0.44,0.82);与癌症相关的器质性 GH 缺乏症患者 SMR 升高[5.87(3.21,9.85)]。基于 18 例病例,2 型糖尿病(T2DM)风险增加[SIR:3.77(2.24,5.96)],但 72%的患者有风险因素。在无癌症病史的患者中,观察到 14 例原发性癌症[SIR:0.71(0.39,1.20)]。31 例癌症幸存者发生第二原发性肿瘤[5.0%;10.7(7.5,15.2)例/1000 人年],823 例肿瘤幸存者中 67 例发生颅内肿瘤复发[8.1%;16.9(13.3,21.5)例/1000 人年]。所有 3 例脑出血病例均有危险因素。
GenesIs(儿童 GH 治疗的遗传和神经内分泌学研究)数据支持儿科 GH 治疗具有良好的安全性。GH 治疗儿童的死亡或原发性癌症总体风险未升高,且无危险因素的患者未发生脑出血。与普通人群相比,T2DM 的发病率升高,但大多数病例均有糖尿病风险因素。