Suppr超能文献

儿童急性淋巴细胞白血病减停激素期间的类固醇撤药综合征:一项在诱导期比较泼尼松与地塞米松的对照研究。

Steroid withdrawal syndrome during steroid tapering in childhood acute lymphoblastic leukemia: a controlled study comparing prednisone versus dexamethasone in induction phase.

作者信息

Saracco Paola, Bertorello Nicoletta, Farinasso Loredana, Einaudi Silvia, Barisone Elena, Altare Franco, Corrias Andrea, Pastore Guido

机构信息

Department of Pediatric Onco-Hematology, University of Turin, Turin, Italy.

出版信息

J Pediatr Hematol Oncol. 2005 Mar;27(3):141-4. doi: 10.1097/01.mph.0000155870.38794.e7.

Abstract

Children with acute lymphoblastic leukemia (ALL) receive as part of induction therapy a 4-week course of high-dose glucocorticoid, which is either abruptly discontinued or shortly tapered. The aim of this study was to evaluate the signs and symptoms of steroid withdrawal syndrome and performance status (according to Lansky scale) during the 9-day tapering period and 1 week after withdrawal of the steroid in 63 children randomly allocated to receive prednisone or dexamethasone as part of induction treatment according the AIEOP ALL 2000 protocol. Twenty of 28 (75%) patients on dexamethasone versus 18 of 35 (51.4%) on prednisone (P < 0.05) developed at least one steroid withdrawal symptom during the study period. Three or more symptoms were observed in 39.3% (11/28) of the dexamethasone group and 8.6% (3/35) of the prednisone group (P < 0.05). Dexamethasone patients developed clinical signs earlier (within 3 days from the steroid tapering) than symptomatic prednisone patients. In the prednisone group, the symptoms were less severe and the performance status was higher (P < 0.05). Steroid withdrawal morbidity in ALL children during induction is a frequent and clinically relevant complaint. A more gradual (for dexamethasone) or a more prolonged (for prednisone) tapering might be suggested.

摘要

急性淋巴细胞白血病(ALL)患儿在诱导治疗期间会接受为期4周的大剂量糖皮质激素治疗,治疗结束后要么突然停药,要么短期减量。本研究旨在评估63名根据AIEOP ALL 2000方案随机分配接受泼尼松或地塞米松作为诱导治疗一部分的儿童在9天减量期及停药后1周内的类固醇戒断综合征体征和症状以及体能状态(根据兰斯基量表)。在研究期间内,接受地塞米松治疗的28名患者中有20名(75%)出现了至少一种类固醇戒断症状,而接受泼尼松治疗的35名患者中有18名(51.4%)出现该症状(P<0.05)。地塞米松组39.3%(11/28)的患者和泼尼松组8.6%(3/35)的患者出现了三种或更多症状(P<0.05)。地塞米松组患者出现临床体征的时间更早(在类固醇减量开始后3天内),而有症状的泼尼松组患者出现较晚。在泼尼松组中,症状较轻,体能状态较高(P<0.05)。ALL患儿诱导治疗期间的类固醇戒断发病率是一种常见且与临床相关的主诉。可能建议采用更缓慢的减量方式(用于地塞米松)或更长时间的减量方式(用于泼尼松)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验