O'Meara A, Daly M, Hallinan F H
Children's Research Centre, Our Lady's Hospital for Sick Children, Dublin, Ireland.
Med Pediatr Oncol. 1988;16(3):169-74. doi: 10.1002/mpo.2950160304.
Previous reports have observed a fall in antithrombin III (AT III) concentration in patients receiving L-asparaginase as part of acute lymphatic leukaemia (ALL) induction therapy. The aim of this study was to define any qualitative changes in AT III that might arise during the course of L-asparaginase therapy and predispose to coagulopathy. Serial AT III profiles were studied in 12 patients with ALL receiving a course of L-asparaginase for 21 consecutive days as part of induction therapy. AT III isoforms were examined by isoelectric focusing in polyacrylamide gels (IEF/PA) and immunoblotting, and no changes were observed throughout the study period. Contrary to expectation, AT III antigen was significantly increased on treatment, while AT III activity remained unchanged. Fibrinogen levels, in contrast, fell considerably by 1 week of therapy and had not reverted to pre-treatment values 1 week after completion of asparaginase. No coagulation or bleeding disorders were observed during or after the study period.
既往报告观察到,接受L-天冬酰胺酶作为急性淋巴细胞白血病(ALL)诱导治疗一部分的患者,其抗凝血酶III(AT III)浓度会下降。本研究的目的是确定在L-天冬酰胺酶治疗过程中可能出现的、易导致凝血病的AT III的任何定性变化。对12例接受L-天冬酰胺酶疗程连续21天作为诱导治疗一部分的ALL患者进行了连续的AT III分析。通过在聚丙烯酰胺凝胶中进行等电聚焦(IEF/PA)和免疫印迹法检测AT III同工型,在整个研究期间未观察到变化。与预期相反,治疗时AT III抗原显著增加,而AT III活性保持不变。相比之下,纤维蛋白原水平在治疗1周时大幅下降,在天冬酰胺酶治疗完成1周后仍未恢复到治疗前水平。在研究期间或之后未观察到凝血或出血障碍。