Sampaio Mafalda, Oliveira Andreia, Soro Isabel, Costa Carla, Castro-Correia Cíntia, Fontoura Manuel
Unidade de Endocrinologia Pediátrica, Serviço de Pediatria, Unidade Autónoma de Gestão da Mulher e da Criança, Hospital de São João, Porto, Portugal.
Acta Med Port. 2011 Dec;24 Suppl 2:393-8. Epub 2011 Dec 31.
Growth hormone (GH) deficiency is one of the most frequent endocrine problems occurring in cancer survivors, particularly when there is a previous history of central nervous system (CNS) tumour and submission to radiotherapy (RT).
We retrospectively assessed pediatric cancer survivors with GH deficiency, submitted to GH treatment from 1988 to 2010 in a tertiary level hospital. We analised the following data: sex, age, oncologic diagnosis, oncologic treatment, auxology, Tanner puberty stage, final height, target height and other associated endocrine problems. We determined the height z-score difference between the beginning and the end of GH treatment (for patients who ended treatment), and between the beginning of GH treatment and the last observation (for patients who are currently on treatment), which was defined as the dependent variable. SPSS® version 17.0 was used for statistical analysis.
A sample of 18 patients was obtained, 12 male, with a median age of cancer diagnosis of six years old. The diagnostics were CNS tumors (n=15) and hematologic neoplasia (n=3). Cancer treatment modalities were craniospinal RT (n=9), cranial RT (n=4), chemotherapy (n=14) and CNS surgery (n=15). The median of time between cancer treatment and beginning of GH treatment was 4 years and 8 months. Height z-score difference was positive in 12 patients. Statistical significant differences between medians and centiles of height z-score difference occurred in patients submitted to craniospinal RT (-0.08), cranial RT (0.59) and no RT (1.56) (p=0.003, IC 95%). The biggest differences between final height and target height (-10 and -11.5 cm) occurred in two patients submitted to craniospinal RT, with associated precocious puberty.
Our results are consistent with previous studies, which point to a lesser efficacy of GH treatment when there is a past history of RT, namely craniospinal RT, and in association with precocious puberty.
生长激素(GH)缺乏是癌症幸存者中最常见的内分泌问题之一,尤其是既往有中枢神经系统(CNS)肿瘤病史并接受过放射治疗(RT)的患者。
我们回顾性评估了1988年至2010年在一家三级医院接受GH治疗的生长激素缺乏的儿科癌症幸存者。我们分析了以下数据:性别、年龄、肿瘤诊断、肿瘤治疗、体格检查、坦纳青春期分期、最终身高、靶身高以及其他相关内分泌问题。我们确定了GH治疗开始与结束时(对于结束治疗的患者)以及GH治疗开始与最后一次观察时(对于仍在接受治疗的患者)的身高z评分差异,该差异被定义为因变量。使用SPSS®17.0版进行统计分析。
共纳入18例患者,其中男性12例,癌症诊断时的中位年龄为6岁。诊断包括中枢神经系统肿瘤(n = 15)和血液系统肿瘤(n = 3)。癌症治疗方式包括全脑全脊髓放疗(n = 9)、颅脑放疗(n = 4)、化疗(n = 14)和中枢神经系统手术(n = 15)。癌症治疗与GH治疗开始之间的中位时间为4年8个月。12例患者的身高z评分差异为正值。接受全脑全脊髓放疗(-0.08)、颅脑放疗(0.59)和未接受放疗(1.56)的患者,身高z评分差异的中位数和百分位数之间存在统计学显著差异(p = 0.003,95%置信区间)。在两名接受全脑全脊髓放疗并伴有性早熟的患者中,最终身高与靶身高之间的差异最大(-10和-11.5厘米)。
我们的结果与先前的研究一致,即既往有放疗史(尤其是全脑全脊髓放疗)且伴有性早熟时,GH治疗的疗效较差。