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Reduced vs. standard dose native E. coli-asparaginase therapy in childhood acute lymphoblastic leukemia: long-term results of the randomized trial Moscow–Berlin 2002

机译:相对于标准剂量的天然大肠杆菌-天冬酰胺酶降低剂量治疗儿童急性淋巴细胞白血病:莫斯科-柏林2002年随机试验的长期结果

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摘要

PurposeFavorable outcomes were achieved for children with acute lymphoblastic leukemia (ALL) with the first Russian multicenter trial Moscow–Berlin (ALL-MB) 91. One major component of this regimen included a total of 18 doses of weekly intramuscular (IM) native Escherichia coli-derived asparaginase (E. coli-ASP) at 10000 U/m2 during three consolidation courses. ASP was initially available from Latvia, but had to be purchased from abroad at substantial costs after the collapse of Soviet Union. Therefore, the subsequent trial ALL-MB 2002 aimed at limiting costs to a reasonable extent and also at reducing toxicity by lowering the dose for standard risk (SR−) patients to 5000 U/m2 without jeopardizing efficacy.
机译:目的首次俄罗斯多中心试验莫斯科–柏林(ALL-MB)91对急性淋巴细胞性白血病(ALL)的儿童取得了有利的结果。该方案的主要组成部分包括每周肌注(IM)天然大肠杆菌共18剂在三个巩固过程中以10000 U / m 2 衍生的天冬酰胺酶(E. coli-ASP)。 ASP最初可从拉脱维亚获得,但在苏联解体后必须从国外购买,价格昂贵。因此,随后的试验ALL-MB 2002旨在在合理范围内限制成本,并通过将标准风险(SR-)患者的剂量降低至5000 U / m 2 来降低毒性,而不会损害疗效。

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