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何时才算足够……足够呢?血友病患者及抑制物患者免疫耐受诱导失败定义的共识达成。

When is enough…enough? Developing consensus of definition of failure of immune tolerance induction in patients with haemophilia and inhibitors.

作者信息

Barnes C, Brown S A, Curtin J, Dunkley S

机构信息

Haemophilia Treatment Centre, Royal Children's Hospital, Parkville, Vic., Australia.

出版信息

Haemophilia. 2014 Jul;20(4):e275-9. doi: 10.1111/hae.12442.

DOI:10.1111/hae.12442
PMID:24948406
Abstract

Immune tolerance induction (ITI) is the preferred management of haemophilia A patients who develop high titre inhibitors against factor VIII. However, the optimal ITI regimen, predictors of ITI outcome and definitions of successful and unsuccessful ITI remain unclear. The aim of this project was to develop a consensus on the definition of ITI treatment failure for Australian clinical practice using a modified Delphi approach. Three consecutive surveys were distributed to the directors of 17 haemophilia treatment centres in Australia. Participants were asked to rate their agreement with definitions of ITI treatment failure generated from a literature review. Thirty-five statements regarding ITI achieved consensus (majority agree or strongly agree) during the three survey rounds. After round 3, four statements achieved majority disagreement, and for two statements no consensus was reached. Our study demonstrates that clinicians in Australia necessitate an arbitrary time to assess ITI failure, but that clinical outcomes of ITI are important in assessing response. Assessment over any 3- to 6-month period without a 20% reduction in inhibitor titre is suggestive of failure, but a reduction in bleeding phenotype alone may be sufficient to continue ITI. Overall, a period of 3 or 5 years of ITI may be required to determine response to ITI. Documentation of improvement in clinical measures, supported by the laboratory features of factor VIII inhibitor levels and pharmacokinetics, is essential in assessing the success of failure of ITI in these patients.

摘要

免疫耐受诱导(ITI)是对产生高滴度抗凝血因子VIII抑制剂的甲型血友病患者的首选治疗方法。然而,最佳的ITI方案、ITI结果的预测因素以及成功和失败的ITI定义仍不明确。本项目的目的是采用改良的德尔菲法,就澳大利亚临床实践中ITI治疗失败的定义达成共识。连续三次调查被分发给澳大利亚17个血友病治疗中心的主任。参与者被要求对他们对文献综述中产生的ITI治疗失败定义的认同程度进行评分。在三轮调查中,35条关于ITI的陈述达成了共识(大多数人同意或强烈同意)。在第三轮之后,有4条陈述得到了大多数人的反对,还有2条陈述未达成共识。我们的研究表明,澳大利亚的临床医生需要一个任意的时间来评估ITI失败,但ITI的临床结果在评估反应方面很重要。在任何3至6个月的时间段内,如果抑制剂滴度没有降低20%,则提示治疗失败,但仅出血表型的改善可能足以继续进行ITI治疗。总体而言,可能需要3年或5年的ITI治疗时间来确定对ITI的反应。在评估这些患者ITI治疗的成功或失败时,由凝血因子VIII抑制剂水平和药代动力学的实验室特征支持的临床测量改善的记录至关重要。

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When is enough…enough? Developing consensus of definition of failure of immune tolerance induction in patients with haemophilia and inhibitors.何时才算足够……足够呢?血友病患者及抑制物患者免疫耐受诱导失败定义的共识达成。
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引用本文的文献

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J Manag Care Spec Pharm. 2021 Aug;27(8):996-1008. doi: 10.18553/jmcp.2021.20600. Epub 2021 Apr 12.
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Experience of Immune Tolerance Induction Therapy for Hemophilia A Patients with Inhibitors from a Single Center in India.印度单中心对血友病A抑制物患者进行免疫耐受诱导治疗的经验
Indian J Hematol Blood Transfus. 2020 Jul;36(3):458-463. doi: 10.1007/s12288-019-01218-2. Epub 2019 Nov 4.
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Inhibitors in haemophilia A and B: Management of bleeds, inhibitor eradication and strategies for difficult-to-treat patients.
血友病 A 和 B 的抑制剂:出血管理、抑制剂清除和治疗困难患者的策略。
Eur J Haematol. 2019 Feb;102(2):111-122. doi: 10.1111/ejh.13193. Epub 2018 Dec 6.