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对大肠杆菌L-天冬酰胺酶的过敏反应不影响儿童B前体急性淋巴细胞白血病的预后:一项儿童肿瘤学组研究。

Allergic reactions to E. coli L-asparaginase do not affect outcome in childhood B-precursor acute lymphoblastic leukemia: a Children's Oncology Group Study.

作者信息

Wacker Pierre, Land Vita J, Camitta Bruce M, Kurtzberg Joanne, Pullen Jeanette, Harris Michael B, Shuster Jonathan J

机构信息

Hôpitaux Universitaires de Genève, Geneva, Switzerland.

出版信息

J Pediatr Hematol Oncol. 2007 Sep;29(9):627-32. doi: 10.1097/MPH.0b013e3181483df1.

Abstract

We describe the outcome of children with B-precursor acute lymphoblastic leukemia registered on Pediatric Oncology Group 8602 who switched to Erwinia asparaginase (ASP) due to an allergy to the Escherichia coli product. Between February 1986 and January 1991, children in complete remission after induction that included intramuscular E. coli ASP (6000 U/m2x6) were randomized for consolidation. One regimen included intensive weekly intramuscular E. coli ASP (25,000 U/m2/wkx24). In case of an allergic reaction to E. coli ASP, Erwinia ASP was substituted at the same dose and schedule. Of the 540 eligible patients, 408 switched to Erwinia ASP due to an allergic reaction. Allergic reactions were significantly associated with younger age, white race, and standard-risk acute lymphoblastic leukemia. Multivariate Cox analysis adjusting for these factors demonstrated no correlation between the switch per se or the timing of the switch and event-free survival.

摘要

我们描述了在儿童肿瘤学组8602注册的B前体急性淋巴细胞白血病患儿的结局,这些患儿因对大肠杆菌来源的天冬酰胺酶(ASP)过敏而改用欧文氏菌天冬酰胺酶。1986年2月至1991年1月期间,诱导治疗后达到完全缓解且诱导治疗包括肌肉注射大肠杆菌ASP(6000 U/m²×6)的患儿被随机分组进行巩固治疗。一种方案包括每周强化肌肉注射大肠杆菌ASP(25,000 U/m²/周×24周)。若对大肠杆菌ASP发生过敏反应,则以相同剂量和疗程改用欧文氏菌ASP。在540例符合条件的患者中,408例因过敏反应改用欧文氏菌ASP。过敏反应与年龄较小、白种人和标准风险急性淋巴细胞白血病显著相关。对这些因素进行校正的多变量Cox分析显示,改用本身或改用时机与无事件生存期之间无相关性。

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