Ver Elst Kristien M M, van Vliet Huub D M, Kappers-Klunne Mies C, Leebeek Frank W G
Department of Haematology, Erasmus Medical Center, 3000 CA Rotterdam, The Netherlands.
Thromb Haemost. 2004 Jul;92(1):67-74. doi: 10.1160/TH04-02-0107.
Patients with type 2 and 3 von Willebrand disease (VWD) are treated with factor VIII/VWF concentrate in case of bleeding or surgery. Immunate (Baxter, Vienna, Austria) is a double virus inactivated FVIII/VWF concentrate and is registered in several countries for patients with VWD with reduced FVIII levels. We performed an in vitro, a pharmacokinetic and a clinical study to evaluate Immunate in VWD. In vitro studies showed a significant variation in VWF levels in 9 different batches. The median (range) values (in IU/mL) were 1.10 (0.98-1.30) for FVIII:C, 1.34 (0.95-1.61) for VWF:Ag, 0.60 (0.27-1.08) for VWF:CBA and 0.73 (0.59-0.94) for VWF:RCo. The relatively low VWF activity is mainly due to the lack of high molecular weight multimers (HMWM), as determined by electrophoresis. A pharmacokinetic study showed, based on a content of FVIII:C of 1 U/mL, in vivo recoveries (%) of 106 (56-150) (median and range) for FVIII:C, 105 (62-187) for VWF:Ag, 25 (7-41) for VWF:CBA and 43 (11-76) for VWF:RCo. Half-lives were 14.1 h (7.4-36.9) for FVIII:C, 10.8 h (7.7-26.2) for VWF:Ag, 15.3 h (7.8-44.6) for VWF:CBA and 16.4 h (4.2-26.5) for VWF:RCo. In a clinical study efficacy was determined after infusion given before surgery or dental extractions in ten patients. In two patients the hemostatic response was classified as inadequate. In conclusion, there is a wide variability in VWF concentration and activity in various batches of Immunate. In the clinical study in which the dosage was based on FVIII:C contents of the concentrate, two out of ten patients had an insufficient haemostatic response. Therefore dosing of Immunate dosing should not be based on FVIII:C levels, but should be based on VWF activity of the individual batches. Future studies using a VWF activity-guided dosage regimen have to be performed to establish the efficacy of Immunate in the treatment of von Willebrand disease.
2型和3型血管性血友病(VWD)患者在出血或手术时用凝血因子VIII/血管性血友病因子(VWF)浓缩物进行治疗。Immunate(百特公司,奥地利维也纳)是一种双重病毒灭活的FVIII/VWF浓缩物,已在多个国家注册用于FVIII水平降低的VWD患者。我们进行了一项体外、药代动力学和临床研究以评估Immunate在VWD中的作用。体外研究显示9个不同批次的VWF水平存在显著差异。FVIII:C的中位数(范围)值(以IU/mL计)为1.10(0.98 - 1.30),VWF:Ag为1.34(0.95 - 1.61),VWF:CBA为0.60(0.27 - 1.08),VWF:RCo为0.73(0.59 - 0.94)。相对较低的VWF活性主要是由于缺乏高分子量多聚体(HMWM),这通过电泳确定。一项药代动力学研究表明,基于FVIII:C含量为1 U/mL,FVIII:C的体内回收率(%)为106(56 - 150)(中位数和范围),VWF:Ag为105(62 - 187),VWF:CBA为25(7 - 41),VWF:RCo为43(11 - 76)。半衰期分别为:FVIII:C为14.1小时(7.4 - 36.9),VWF:Ag为10.8小时(7.7 - 26.2),VWF:CBA为15.3小时(7.8 - 44.6),VWF:RCo为16.4小时(4.2 - 26.5)。在一项临床研究中,对10例患者在手术或拔牙前输注后确定疗效。2例患者的止血反应被分类为不足。总之,不同批次的Immunate中VWF浓度和活性存在很大差异。在基于浓缩物FVIII:C含量进行剂量设定的临床研究中,10例患者中有2例止血反应不足。因此,Immunate的给药不应基于FVIII:C水平而应基于各批次的VWF活性。必须进行未来使用VWF活性指导剂量方案的研究以确定Immunate在治疗血管性血友病中的疗效。