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载门冬酰胺酶的红细胞在儿童和成人难治或复发急性淋巴细胞白血病中的应用:GRASPALL2005-01 随机试验结果。

l-asparaginase loaded red blood cells in refractory or relapsing acute lymphoblastic leukaemia in children and adults: results of the GRASPALL 2005-01 randomized trial.

机构信息

Institut d'Hemato-Oncologie pédiatrique, Hospices civils de Lyon, Université Claude Bernard, France.

出版信息

Br J Haematol. 2011 Apr;153(1):58-65. doi: 10.1111/j.1365-2141.2011.08588.x. Epub 2011 Feb 20.

Abstract

l-asparaginase encapsulated within erythrocytes (GRASPA(®) ) should allow serum asparagine depletion over a longer period than the native form of the enzyme, using lower doses and allowing better tolerance. The GRASPALL 2005-01 study, a multicentre randomized controlled trial, investigated three doses of GRASPA(®) for the duration of asparagine depletion in a phase I/II study in adults and children with acute lymphoblastic leukaemia (ALL) in first relapse. Between February 2006 and April 2008, 18 patients received GRASPA(®) (50 iu/kg: n = 6,100 iu/kg: n = 6, 150 iu/kg: n = 6) after randomization, and six patients were assigned to the Escherichia coli native l-asparaginase (E. colil-ASNase) control group. GRASPA(®) was effective at depleting l-asparagine. One single injection of 150 iu/kg of GRASPA(®) provided similar results to 8 × 10,000 iu/m(2) intravenous injections of E. colil-ASNase. The safety profile of GRASPA(®) showed a reduction in the number and severity of allergic reactions and a trend towards less coagulation disorders. Other expected adverse events were comparable to those observed with E. colil-ASNase and there was also no difference between the three doses of GRASPA(®) .

摘要

用红细胞包裹的 L-天冬酰胺酶(GRASPA(®))应该能够比天然形式的酶更长时间地耗尽血清中的天冬酰胺,使用更低的剂量,并允许更好的耐受性。GRASPALL 2005-01 研究是一项多中心随机对照试验,在成人和儿童急性淋巴细胞白血病(ALL)首次复发的 I/II 期研究中,调查了 GRASPA(®)三种剂量在天冬酰胺耗竭期间的应用。在 2006 年 2 月至 2008 年 4 月期间,18 名患者在随机分组后接受了 GRASPA(®)(50 iu/kg:n = 6,1000 iu/kg:n = 6,150 iu/kg:n = 6)治疗,6 名患者被分配到大肠杆菌天然 L-天冬酰胺酶(E. colil-ASNase)对照组。GRASPA(®)能有效耗尽 L-天冬酰胺。单次注射 150 iu/kg 的 GRASPA(®)与 8 次 10000 iu/m2 静脉注射 E. colil-ASNase 提供了相似的结果。GRASPA(®)的安全性特征显示过敏反应的次数和严重程度减少,且凝血障碍的趋势也较少。其他预期的不良事件与 E. colil-ASNase 观察到的相似,而且 GRASPA(®)的三种剂量之间也没有差异。

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