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首页> 外文期刊>Pediatric blood & cancer >Neurobehavioral side effects of corticosteroids during active treatment for acute lymphoblastic leukemia in children are age-dependent: report from Dana-Farber Cancer Institute ALL Consortium Protocol 00-01.
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Neurobehavioral side effects of corticosteroids during active treatment for acute lymphoblastic leukemia in children are age-dependent: report from Dana-Farber Cancer Institute ALL Consortium Protocol 00-01.

机译:积极治疗儿童急性淋巴细胞白血病期间糖皮质激素的神经行为副作用是年龄依赖性的:Dana-Farber Cancer Institute ALL Consortium Protocol 00-01的报告。

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摘要

BACKGROUND: Although corticosteroids remain a mainstay of treatment for acute lymphoblastic leukemia (ALL), they can cause troublesome neurobehavioral changes during active treatment, especially in young children. We evaluated acute neurobehavioral side effects of corticosteroid therapy in preschool versus school-age children by obtaining structured reports weekly for 1 month. PROCEDURE: Parents of 62 children (2-17 years) treated on Dana-Farber Cancer Institute (DFCI) ALL Consortium Protocol 00-01 participated during the continuation phase of treatment. Patients received cyclical twice-daily 5-day courses of prednisone (PRED; 40 mg/m(2) /day) or dexamethasone (DEX; 6 mg/m(2) /day). Parents completed behavior rating scales about their child weekly during one steroid cycle [baseline (Day 0), active steroid (Day 7), post-steroid (Days 14 and 21)]. RESULTS: Behavioral side effects increased significantly (P < 0.001) during the steroid week for preschool children (<6 years) on measures of emotional control, mood, behavior regulation, and executive functions, returning to baseline during the two "off-steroid" weeks. In contrast, school-age children (>/= 6 years) did not demonstrate an increase in side effects during the steroid week. Steroid type (PRED vs. DEX) was not a significant predictor of neurobehavioral side effects. CONCLUSIONS: Preschool children are at greater risk for neurobehavioral side effects during active steroid treatment for ALL than school-age children and adolescents. DEX was not associated with more neurobehavioral side effects than PRED. Counseling of families about side-effects should be adapted according to age. The observed effects, moreover, were transient, reducing concerns about longer-term neurobehavioral toxicities.
机译:背景:尽管皮质类固醇仍是急性淋巴细胞白血病(ALL)治疗的主要手段,但它们在积极治疗期间可能引起麻烦的神经行为改变,尤其是在幼儿中。通过评估每周1个月的结构化报告,我们评估了皮质类固醇疗法在学龄前儿童与学龄儿童中的急性神经行为副作用。程序:接受Dana-Farber癌症研究所(DFCI)ALL Consortium 00-01协议治疗的62名儿童(2-17岁)的父母参加了治疗的继续阶段。患者接受泼尼松(PRED; 40 mg / m(2)/天)或地塞米松(DEX; 6 mg / m(2)/天)的周期性每日两次5天疗程。父母在一个类固醇周期[基线(第0天),活动类固醇(第7天),类固醇后(第14和21天)]每周完成关于孩子的行为评估量表。结果:学龄前儿童(<6岁)在类固醇周期间的行为控制,情绪调节,行为调节和执行功能等方面的行为副作用显着增加(P <0.001),在两次“类固醇关闭”期间恢复到基线周。相反,学龄儿童(> / = 6岁)在类固醇周期间未显示出副作用增加。类固醇类型(PRED与DEX)不是神经行为副作用的重要预测指标。结论:与学龄儿童和青少年相比,在对类固醇进行有效激素治疗期间,学龄前儿童发生神经行为副作用的风险更大。 DEX与PRED相比没有更多的神经行为副作用。家庭的副作用咨询应根据年龄进行调整。此外,观察到的效果是短暂的,从而减少了对长期神经行为毒性的担忧。

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