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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.

DOI:10.1002/jha2.714
PMID:37601872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10435701/
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
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9e0/10435701/a0954d54845e/JHA2-4-710-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9e0/10435701/a0954d54845e/JHA2-4-710-g001.jpg

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Normalisation of haemoglobin and control of breakthrough haemolysis with increased frequency pegcetacoplan dosing in treated paroxysmal nocturnal haemoglobinuria.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。
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本文引用的文献

1
Inhibition of C3 with pegcetacoplan results in normalization of hemolysis markers in paroxysmal nocturnal hemoglobinuria.佩格司他单抗抑制 C3 可使阵发性睡眠性血红蛋白尿症的溶血标志物恢复正常。
Ann Hematol. 2022 Sep;101(9):1971-1986. doi: 10.1007/s00277-022-04903-x. Epub 2022 Jul 22.
2
Breakthrough Hemolysis in PNH with Proximal or Terminal Complement Inhibition.阵发性睡眠性血红蛋白尿症中近端或末端补体抑制引发的突破性溶血
N Engl J Med. 2022 Jul 14;387(2):160-166. doi: 10.1056/NEJMra2201664.
3
Pegcetacoplan versus Eculizumab in Paroxysmal Nocturnal Hemoglobinuria.
佩格司他单抗与依库珠单抗治疗阵发性睡眠性血红蛋白尿症的疗效比较。
N Engl J Med. 2021 Mar 18;384(11):1028-1037. doi: 10.1056/NEJMoa2029073.
4
Anti-complement Treatment for Paroxysmal Nocturnal Hemoglobinuria: Time for Proximal Complement Inhibition? A Position Paper From the SAAWP of the EBMT.抗补体治疗阵发性睡眠性血红蛋白尿症:是否需要近端补体抑制?来自 EBMT 的 SAAWP 的立场文件。
Front Immunol. 2019 Jun 14;10:1157. doi: 10.3389/fimmu.2019.01157. eCollection 2019.
5
Ravulizumab (ALXN1210) vs eculizumab in adult patients with PNH naive to complement inhibitors: the 301 study.瑞维鲁单抗(ALXN1210)与依库珠单抗在既往未接受补体抑制剂治疗的成人 PNH 患者中的比较:301 研究。
Blood. 2019 Feb 7;133(6):530-539. doi: 10.1182/blood-2018-09-876136. Epub 2018 Dec 3.
6
Ravulizumab (ALXN1210) vs eculizumab in C5-inhibitor-experienced adult patients with PNH: the 302 study.瑞维鲁单抗(ALXN1210)对比依库珠单抗在有 C5 抑制剂治疗史的成人 PNH 患者中的疗效:302 研究。
Blood. 2019 Feb 7;133(6):540-549. doi: 10.1182/blood-2018-09-876805. Epub 2018 Dec 3.
7
Long-term treatment with eculizumab in paroxysmal nocturnal hemoglobinuria: sustained efficacy and improved survival.依库珠单抗长期治疗阵发性睡眠性血红蛋白尿症:疗效持续且生存改善。
Blood. 2011 Jun 23;117(25):6786-92. doi: 10.1182/blood-2011-02-333997. Epub 2011 Apr 1.
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Blood. 2009 Apr 23;113(17):4094-100. doi: 10.1182/blood-2008-11-189944. Epub 2009 Jan 29.
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Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria.补体抑制剂依库珠单抗治疗阵发性夜间血红蛋白尿症患者的多中心3期研究。
Blood. 2008 Feb 15;111(4):1840-7. doi: 10.1182/blood-2007-06-094136. Epub 2007 Nov 30.
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The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria.补体抑制剂依库珠单抗治疗阵发性夜间血红蛋白尿症。
N Engl J Med. 2006 Sep 21;355(12):1233-43. doi: 10.1056/NEJMoa061648.