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Monitoring of Erwinia asparaginase therapy in childhood ALL in the Nordic countries.

机译:北欧国家儿童ALL中欧文氏菌天冬酰胺酶治疗的监测。

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AIMS: Evaluation of L-asparaginase therapy in the NOPHO-92 ALL-protocol (treatment protocol of acute lymphoblastic leukaemia of the Nordic Society of Paediatric Haematology and Oncology, initiated in 1992) after intravenous and intramuscular administration of Erwinia asparaginase during induction and re-induction therapy. METHODS: Forty children with newly diagnosed acute lymphoblastic leukaemia received Erwinia asparaginase (30 000 IU/m2 i.v. or i.m.) during induction therapy (every day for 10 days), and 19 children received Erwinia asparaginase (30 000 IU/m2 i.v. or i.m.) during re-induction therapy (twice a week for 2 weeks). Within the treatment periods asparaginase trough activity (using a spectrophotometric assay) was determined on specific days. The goal of therapy is complete L-asparagine depletion, which asparaginase activities above 100 IU l(-1) have been shown to ensure. Therefore determination of L-asparagine (using a h.p.l.c. method) was performed only in plasma samples with asparaginase activities below 100 IU l(-1). RESULTS: During induction therapy 92.2% of the trough enzyme activities were above 500 IU l(-1) for the i.v.-treated patients, and 92.4% of the trough enzyme activities were above 500 IU l(-1) for the i.m.-treated patients. During re-induction therapy 64.7% of the trough enzyme activities were below 100 IU l(-1) in the i.v.-treated group, and 73.3% of the trough enzyme activities were below 100 IU l(-1) in the i.m.-treated group. For trough enzyme activities below 100 IU l(-1) L-asparagine depletion was complete in two thirds of the samples. CONCLUSIONS: In the NOPHO-92 ALL-protocol L-asparaginase treatment during induction therapy was unnecessarily intense, but during the re-induction phase it appeared inadequate.
机译:目的:在诱导和再灌注期间静脉内和肌肉内注射艾尔文氏菌门冬酰胺酶后,评估NOPHO-92 ALL方案中L-天冬酰胺酶疗法的疗效(北欧小儿血液病和肿瘤学会急性淋巴细胞白血病的治疗方案,始于1992年)。诱导疗法。方法:40名新诊断为急性淋巴细胞白血病的儿童在诱导治疗期间(每天,共10天)接受了艾尔文氏菌天冬酰胺酶(30000 IU / m2 iv或im),19名儿童接受了艾尔文氏菌天冬酰胺酶(30000 IU / m2 iv或im)。在重新诱导治疗期间(每周两次,共2周)。在治疗期间内,在特定日期确定天冬酰胺酶谷活性(使用分光光度测定法)。治疗的目标是完全消耗L-天冬酰胺,已证明可以确保100 IU l(-1)以上的天冬酰胺酶活性。因此,仅在天冬酰胺酶活性低于100 IU l(-1)的血浆样品中进行L-天冬酰胺测定(使用h.p.l.c.方法)。结果:诱导治疗期间,静脉注射治疗的患者中92.2%的谷类酶活性高于500 IU l(-1),而静脉注射治疗的患者中92.4%的谷类酶活性高于500 IU l(-1)耐心。在再诱导疗法中,静脉注射治疗组中64.7%的谷类酶活性低于100 IU l(-1),而静脉注射治疗组中73.3%的谷类酶活性低于100 IU l(-1)组。对于低于100 IU l(-1)的低谷酶活性,三分之二的样品中L-天冬酰胺的消耗完成。结论:在NOPHO-92 ALL方案L-天冬酰胺酶诱导治疗期间,治疗强度过大,但在再诱导阶段则显得不足。

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