首页> 外文期刊>Medical and Pediatric Oncology: The Official Journal of the American Association for Cancer Education >Dosimetry and growth hormone deficiency following cranial irradiation of childhood brain tumors.
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Dosimetry and growth hormone deficiency following cranial irradiation of childhood brain tumors.

机译:儿童脑肿瘤颅内照射后的剂量测定法和生长激素缺乏症。

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BACKGROUND: Dosimetry of the hypothalamus-pituitary (HP) region could allow prediction of the risk of growth hormone deficiency (GHD) following cranial irradiation. PROCEDURE: Nineteen children (15 boys) with a median age of 6.3 years (range 1.7-16.5) at the time of irradiation of a brain tumor not involving the HP axis were followed for 1.2-6.3 years (median 3.4) from radiotherapy (RT). The dose to a standardized anatomical model including the HP region was calculated from dose-volume histograms of 10% to 100% in steps of 10% of the HP model based on data from a computer-based treatment planning system. If GHD was suspected from insulin-like growth factor-I, serum insulin-like growth factor binding protein-3, and/or height velocity measurements, an arginine stimulation test was performed. GHD was defined by a peak GH <15mU/liter. RESULTS: Ten patients developed GHD 10-26 months from irradiation. Cox regression analysis identified the 90% dose-volume of the HP box as the strongest predictor of development of GHD (P = 0.03). The median dose to the 90% dose-volume of the HP region was 37.5 Gy (range 2. 3-55.3). The cumulated risk of GHD 2.5 years after radiotherapy for children receiving more than and less than 37.5 Gy to the HP region was 87% and 33%, respectively (P = 0.036). CONCLUSIONS: Dosimetry of a defined HP volume provides the opportunity to 1) calculate the exact dose delivered to this region, 2) predict the risk of GHD and, 3) in the future revise the treatment planning and thus reduce the risk of endocrine adverse effects. Copyright 1999 Wiley-Liss, Inc.
机译:背景:下丘脑-垂体(HP)区域的剂量测定可以预测颅骨照射后生长激素缺乏症(GHD)的风险。程序:19名儿童(15名男孩)在接受不涉及HP轴的脑肿瘤照射时的中位年龄为6.3岁(范围1.7-16.5),接受了放疗(RT)的1.2-6.3年(中位数3.4) )。基于来自基于计算机的治疗计划系统的数据,从10%到100%的剂量体积直方图以HP模型的10%为步长,计算出包含HP区域的标准化解剖模型的剂量。如果从胰岛素样生长因子-1,血清胰岛素样生长因子结合蛋白-3和/或身高速度测量中怀疑存在GHD,则进行精氨酸刺激试验。 GHD由峰值GH <15mU /升定义。结果:十名患者在放疗后10-26个月出现GHD。 Cox回归分析确定HP药盒的90%剂量是GHD发生的最强预测因子(P = 0.03)。 HP区域90%剂量体积的中位剂量为37.5 Gy(范围2. 3-55.3)。放疗后2.5年,接受HP大于或小于37.5 Gy的儿童的GHD累积风险分别为87%和33%(P = 0.036)。结论:确定的HP剂量的剂量测定提供了以下机会:1)计算向该区域递送的确切剂量,2)预测GHD的风险以及3)将来修订治疗计划,从而降低内分泌不良反应的风险。版权所有1999 Wiley-Liss,Inc.

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