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儿童急性淋巴细胞白血病中天冬酰胺酶治疗继发的获得性抗凝血酶III缺乏症。

Acquired antithrombin III deficiency secondary to asparaginase therapy in childhood acute lymphoblastic leukaemia.

作者信息

Andrew M, Brooker L, Mitchell L

机构信息

Department of Paediatrics, McMaster University, Hamilton, Ontario, Canada.

出版信息

Blood Coagul Fibrinolysis. 1994 Jan;5 Suppl 1:S24-36; discussion S59-64. doi: 10.1097/00001721-199401000-00005.

Abstract

As improved treatment regimens for acute lymphoblastic leukaemia (ALL) continue to improve survival future, therapy must also take into consideration the many secondary problems. Most of these are the direct result of combination chemotherapy and L-asparaginase (ASP), is an example of a highly effective chemotherapeutic agent with serious side-effects such as thromboembolic events. ASP interferes with protein synthesis resulting in an acquired deficiency of antithrombin III. This review explores the effects of ALL and ASP on haemostasis, and the link between ASP and thromboembolic events in childhood ALL.

摘要

随着急性淋巴细胞白血病(ALL)治疗方案的不断改进,患者生存率持续提高,未来的治疗也必须考虑到许多继发性问题。其中大多数是联合化疗的直接结果,而L-天冬酰胺酶(ASP)就是一种高效化疗药物,但会产生严重副作用,如血栓栓塞事件。ASP干扰蛋白质合成,导致抗凝血酶III后天性缺乏。本综述探讨了ALL和ASP对止血的影响,以及ASP与儿童ALL血栓栓塞事件之间的联系。

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