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在澳大利亚患有高滴度抑制物的儿童重度甲型血友病患者中,使用含或不含免疫抑制的凝血因子 VIII/血管性血友病因子浓缩物(BIOSTATE)诱导免疫耐受:一项多中心回顾性研究。

Immune tolerance induction using a factor VIII/von Willebrand factor concentrate (BIOSTATE), with or without immunosuppression, in Australian paediatric severe haemophilia A patients with high titre inhibitors: a multicentre, retrospective study.

作者信息

Robertson Jeremy D, Higgins Pauline, Price Jamie, Dunkley Scott, Barrese Giulio, Curtin Julie

机构信息

Royal Children's Hospital, Brisbane, Queensland, Australia.

Princess Margaret Hospital, Perth, Western Australia, Australia.

出版信息

Thromb Res. 2014 Nov;134(5):1046-51. doi: 10.1016/j.thromres.2014.09.010. Epub 2014 Sep 21.

Abstract

INTRODUCTION

It has been postulated that factor VIII (FVIII) products containing von Willebrand factor (VWF) may improve immune tolerance induction (ITI) success rate in patients with haemophilia A and poor prognostic factors.

MATERIALS AND METHODS

We conducted a retrospective cohort analysis of a FVIII/VWF concentrate (BIOSTATE) for ITI in paediatric patients with severe haemophilia A (SHA) and inhibitors, from January 2003 to December 2011 at 3 paediatric-only Haemophilia Treatment Centres in Australia. Response to ITI was assessed at or before 33 months and at completion of ITI. Fifteen male patients with SHA were included in the analysis.

RESULTS

BIOSTATE was used for primary ITI in 8 patients (2 years, range 1.1-11.5 years) and for salvage ITI in 7 patients (9.9 years, range 1.1-15.4). At the end of the observation period there were 11 patients who achieved a complete response with BIOSTATE after a median duration of 21 months (range 5-85 months); a partial response was achieved in 2 patients in whom ITI is ongoing. Therefore, the overall response rate was 86.6%. Two patients were deemed treatment failures: one due to non-compliance after 18 months of ITI and another in whom a partial response had not been achieved after 22 months of ITI.

CONCLUSION

BIOSTATE was well-tolerated and effective when used for primary or salvage ITI in this cohort of paediatric patients with SHA and a high-level inhibitor.

摘要

引言

据推测,含有血管性血友病因子(VWF)的凝血因子VIII(FVIII)产品可能会提高甲型血友病且预后因素较差患者的免疫耐受诱导(ITI)成功率。

材料与方法

我们对2003年1月至2011年12月期间在澳大利亚3家仅收治儿科患者的血友病治疗中心,使用FVIII/VWF浓缩物(BIOSTATE)对患有严重甲型血友病(SHA)和抑制剂的儿科患者进行ITI的情况进行了回顾性队列分析。在33个月及之前以及ITI结束时评估对ITI的反应。15名患有SHA的男性患者纳入分析。

结果

8名患者(年龄2岁,范围1.1 - 11.5岁)使用BIOSTATE进行初始ITI,7名患者(年龄9.9岁,范围1.1 - 15.4岁)使用其进行挽救性ITI。在观察期结束时,11名患者在中位持续时间21个月(范围5 - 85个月)后对BIOSTATE取得完全反应;2名ITI仍在进行的患者取得部分反应。因此,总体反应率为86.6%。2名患者被视为治疗失败:1名在ITI 18个月后因不依从治疗,另1名在ITI 22个月后未取得部分反应。

结论

在这组患有SHA和高滴度抑制剂的儿科患者中,BIOSTATE用于初始或挽救性ITI时耐受性良好且有效。

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