Department of Pediatrics, Leiden University Medical Centre, Leiden, the Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Clin Endocrinol (Oxf). 2022 Nov;97(5):596-603. doi: 10.1111/cen.14782. Epub 2022 Jun 1.
Hematopoietic stem cell transplantation (HSCT) can be a curative treatment for malignant and nonmalignant diseases in children but is associated with significant late effects including growth failure. Growth hormone treatment (GHRx) is offered to improve growth, but limited data are available on its effect on adult height (AH). We aim to evaluate the effectiveness of GHRx.
Single-center retrospective study.
Thirty-four patients who had received GHRx for ≥1 year were matched with two controls each, without GHRx, based on sex, indication for HSCT (malignancy, benign haematological disease or immunodeficiency), age at HSCT and conditioning with/without total body irradiation (TBI). All had reached AH.
The primary outcome measure was the difference between AH and predicted AH (PAH) at start of GHRx or the equivalent age in controls (AH-PAH), calculated according to Bailey and Pinneau.
GHRx was started at age 12.0 ± 2.6 years; median treatment duration was 3.8 years (range 1.7-9.2). AH-PAH standard deviation score (SDS) was significantly higher in growth hormone (GH) treated boys (-0.5 ± 0.7 SDS) than in controls (-1.5 ± 1.0 SDS, p < .001). Girls also had a higher AH-PAH after GHRx (+0.5 ± 0.6 SDS) compared to controls (-0.2 SDS ±0.7, p < .01). AH remained approximately 2 SDS below target height (TH) in treated and untreated individuals. Among GH-treated children, AH-PAH was higher in those who had received busulfan-based compared to TBI-based conditioning.
GHRx had a significant positive effect on AH compared to PAH, although AH remained far below TH. Higher AH-PAH was observed in girls and in those conditioned without TBI.
造血干细胞移植(HSCT)可作为儿童恶性和非恶性疾病的一种根治性治疗方法,但与显著的晚期效应相关,包括生长障碍。生长激素治疗(GHRx)用于改善生长,但关于其对成人身高(AH)的影响的数据有限。我们旨在评估 GHRx 的有效性。
单中心回顾性研究。
34 名患者接受 GHRx 治疗≥1 年,并根据性别、HSCT 适应证(恶性肿瘤、良性血液疾病或免疫缺陷)、HSCT 时年龄以及是否接受全身照射(TBI)与/或不含 TBI 进行匹配,各匹配两名未接受 GHRx 治疗的对照组患者。所有患者均达到 AH。
主要观察指标是 GHRx 开始时的 AH 与预测 AH(PAH)之间的差异(AH-PAH)或对照组中相当年龄的 PAH(AH-PAH),根据 Bailey 和 Pinneau 计算。
GHRx 开始于 12.0±2.6 岁;中位治疗时间为 3.8 年(范围 1.7-9.2)。接受 GHRx 的男孩(-0.5±0.7 SDS)的 AH-PAH 标准差评分(SDS)显著高于对照组(-1.5±1.0 SDS,p<0.001)。与对照组相比(-0.2 SDS±0.7,p<0.01),接受 GHRx 的女孩的 AH-PAH 也更高(+0.5±0.6 SDS)。接受治疗和未接受治疗的个体的 AH 仍比目标身高(TH)低约 2 SDS。在接受 GHRx 的儿童中,与接受 TBI 为基础的预处理相比,接受以白消安为基础的预处理的儿童的 AH-PAH 更高。
与 PAH 相比,GHRx 对 AH 有显著的积极影响,但 AH 仍远低于 TH。在女孩和未接受 TBI 预处理的儿童中,观察到更高的 AH-PAH。