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在接受治疗的阵发性夜间血红蛋白尿患者中,通过增加聚乙二醇化依库珠单抗给药频率实现血红蛋白正常化并控制突破性溶血。

Normalisation of haemoglobin and control of breakthrough haemolysis with increased frequency pegcetacoplan dosing in treated paroxysmal nocturnal haemoglobinuria.

作者信息

Davis Amanda K, Bingham Nicholas, Szer Jeff

机构信息

Department of Haematology The Alfred Hospital Melbourne Victoria Australia.

Clinical Haematology Royal Melbourne Hospital Melbourne Victoria Australia.

出版信息

EJHaem. 2023 May 23;4(3):710-713. doi: 10.1002/jha2.714. eCollection 2023 Aug.

Abstract

Paroxysmal nocturnal haemoglobinura is an acquired life-threatening haemolytic condition, which is generally well controlled with terminal complement blockade with eculizumab. Whilst almost all patients treated with terminal complement inhibitors develop extravascular haemolysis, only a small proportion of these results in symptomatic anaemia limiting their activities and requiring red cell transfusion. This case highlights the potential role for the C3 inhibitor, pegcetacoplan, in controlling both intravascular and extravascular haemolysis, and is the first case to report on the use of additional doses of pegcetacoplan to control breakthrough haemolysis.

摘要

阵发性夜间血红蛋白尿是一种后天获得性的、危及生命的溶血性疾病,通常通过使用依库珠单抗进行终末补体阻断来得到良好控制。虽然几乎所有接受终末补体抑制剂治疗的患者都会发生血管外溶血,但其中只有一小部分会导致有症状的贫血,限制其活动并需要红细胞输血。本病例突出了C3抑制剂培戈西普在控制血管内和血管外溶血方面的潜在作用,并且是首例报道使用额外剂量的培戈西普来控制突破性溶血的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9e0/10435701/a0954d54845e/JHA2-4-710-g001.jpg

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