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前瞻性、实时监测聚乙二醇化大肠杆菌和欧文氏菌天冬酰胺酶在比利时儿童急性淋巴细胞白血病和非霍奇金淋巴瘤中的治疗作用。

Prospective, real-time monitoring of pegylated Escherichia coli and Erwinia asparaginase therapy in childhood acute lymphoblastic leukaemia and non-Hodgkin lymphoma in Belgium.

机构信息

Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital and Cancer Research Institute Ghent, Ghent, Belgium.

Pediatric Hematology-Oncology, Hôpital Universitaire des Enfants Reine Fabiola (HUDERF-UKZKF), Brussels, Belgium.

出版信息

Br J Haematol. 2020 Jul;190(1):105-114. doi: 10.1111/bjh.16495. Epub 2020 Feb 14.

Abstract

Asparaginase (ASNase) is an important anti-leukaemic drug in the treatment of childhood acute lymphoblastic leukaemia (ALL) and non-Hodgkin lymphoma (NHL). A substantial proportion of patients develop hypersensitivity reactions with anti-ASNase neutralising antibodies, resulting in allergic reactions or silent inactivation (SI), and characterised by inactivation and rapid clearance of ASNase. We report results of a prospective, real-time therapeutic drug monitoring of pegylated Escherichia coli (PEG-)ASNase and Erwinia ASNase in children treated for ALL and NHL in Belgium. Erwinia ASNase was given as second-line after hypersensitivity to PEG-ASNase. In total, 286 children were enrolled in the PEG-ASNase cohort. Allergy was seen in 11·2% and SI in 5·2% of patients. Of the 42 patients treated with Erwinia ASNase, 7·1% experienced allergy and 2·4% SI. The median trough PEG-ASNase activity was high in all patients without hypersensitivity. After Erwinia administration significantly more day 3 samples had activities <100 IU/l (62·5% vs. 10% at day 2 (D2)). The median D2 activity was significantly higher for intramuscular (IM; 347 IU/l) than for intravenous Erwinia administrations (159 IU/l). This prospective, multicentre study shows that monitoring of ASNase activity during treatment of children with ALL and NHL is feasible and informative. Treatment with Erwinia ASNase warrants close monitoring and optimally adherence to a 2-day interval of IM administrations.

摘要

天冬酰胺酶(ASNase)是治疗儿童急性淋巴细胞白血病(ALL)和非霍奇金淋巴瘤(NHL)的重要抗白血病药物。相当一部分患者会产生针对抗 ASNase 中和抗体的过敏反应,导致过敏反应或沉默失活(SI),其特征是 ASNase 失活和快速清除。我们报告了在比利时接受 ALL 和 NHL 治疗的儿童中聚乙二醇(PEG)-ASNase 和欧文氏菌 ASNase 的前瞻性实时治疗药物监测结果。在对 PEG-ASNase 过敏后,给予欧文氏菌 ASNase 作为二线药物。共有 286 名儿童入组 PEG-ASNase 队列。11.2%的患者出现过敏,5.2%的患者出现 SI。在接受欧文氏菌 ASNase 治疗的 42 名患者中,7.1%出现过敏,2.4%出现 SI。所有无过敏患者的 PEG-ASNase 终末浓度均较高。Erwinia 给药后,第 3 天有活性<100IU/L 的样本明显增多(第 2 天为 62.5%,第 3 天为 10%)。肌肉内(IM)给药的第 2 天(D2)活性中位数明显高于静脉内 Erwinia 给药(347IU/l 与 159IU/l)。这项前瞻性、多中心研究表明,在治疗 ALL 和 NHL 儿童时,监测 ASNase 活性是可行且有信息意义的。用欧文氏菌 ASNase 治疗需要密切监测,最好遵循 2 天 IM 给药间隔。

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