Jarfelt M, Bjarnason R, Lannering B
Department of Pediatrics, Division of Hematology and Oncology, Sahlgrenska Academy of Göteborg University, Göteborg, Sweden.
Pediatr Blood Cancer. 2004 Jun;42(7):582-8. doi: 10.1002/pbc.20020.
Young adults who are long-term survivors of acute lymphoblastic leukaemia (ALL) in early childhood usually do well and do not have to go to regular medical checkups. Many of these survivors did receive prophylactic cranial radiotherapy during their oncological treatment. The effect of cranial irradiation on the hypothalamus is considered to be progressive. Therefore, late effects, such as reduced growth hormone (GH) secretion, may remain undetected until adulthood.
Records from all patients treated for ALL before the onset of puberty in the region of West Sweden, between 1 January 1973 and 31 December 1985 were included, provided they were in first remission with a minimum follow-up time of 15 years, and a minimum age of 20. These criteria were met by 47 young adults aged 20-32 years, of whom 35 agreed to participate. We studied spontaneous GH secretion over 24 hr, IGF-I and IGFBP-3, final height and BMI. The patients had been treated according to three consecutive Swedish childhood leukaemia group protocols. The median follow-up time was 20 years, and 19 of the patients had been treated with cranial irradiation (CRT+), 16 had not (CRT-).
CRT+ patients had significantly lower maximal peaks of GH than CRT- patients. Fifty percent of the CRT+ patients had a GH(max) below the cut-off level (3.3 microg/l), for GH treatment. CRT- patients all had GH(max) levels considered within the normal range. Final height of all the patients, except one CRT+ women, was in the range of expected midparental height, the median loss in final height in the CRT+ patients was 0.8 standard deviation (SD). No patient in this study was obese by definition (BMI <30 kg/m(2)). IGF-I and IGFBP-3 concentrations did not correlate to variations in spontaneous GH secretion in these patients.
In spite of the little effect on final height, we found impaired spontaneous GH secretion in 79% of young adults 20-32 years of age, and GH deficiency (GHD) in 47% after low-dose cranial irradiation in early childhood. The consequences of this low-GH secretion need to be investigated.
幼年急性淋巴细胞白血病(ALL)的长期存活的年轻成年人通常情况良好,无需定期进行医学检查。这些幸存者中的许多人在肿瘤治疗期间接受了预防性颅脑放疗。颅脑照射对下丘脑的影响被认为是渐进性的。因此,诸如生长激素(GH)分泌减少等晚期效应可能直到成年才被发现。
纳入了1973年1月1日至1985年12月31日期间在瑞典西部地区青春期前接受ALL治疗的所有患者的记录,条件是他们处于首次缓解期,随访时间至少15年,且年龄至少20岁。47名年龄在20 - 32岁的年轻成年人符合这些标准,其中35人同意参与。我们研究了24小时内的自发性GH分泌、胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子结合蛋白-3(IGFBP-3)、最终身高和体重指数(BMI)。这些患者按照瑞典儿童白血病组的三个连续方案进行治疗。中位随访时间为20年,其中19名患者接受了颅脑照射(CRT+),16名未接受(CRT-)。
CRT+患者的GH最大峰值显著低于CRT-患者。50%的CRT+患者的GH(max)低于用于GH治疗的临界水平(3.3微克/升)。CRT-患者的GH(max)水平均被认为在正常范围内。除一名CRT+女性外,所有患者的最终身高均在预期的父母平均身高范围内,CRT+患者最终身高的中位损失为0.8标准差(SD)。根据定义,本研究中没有患者肥胖(BMI <30千克/平方米)。IGF-I和IGFBP-3浓度与这些患者自发性GH分泌的变化无关。
尽管对最终身高影响较小,但我们发现79%的20 - 32岁年轻成年人自发性GH分泌受损,47%的人在幼年接受低剂量颅脑照射后存在生长激素缺乏(GHD)。这种低GH分泌的后果需要进行研究。