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[阵发性睡眠性血红蛋白尿的管理:最新进展]

[Management of paroxysmal nocturnal hemoglobinuria: an update].

作者信息

Kawaguchi Tatsuya

机构信息

Department of Medical Technology, Kumamoto Health Science University.

出版信息

Rinsho Ketsueki. 2018;59(6):703-710. doi: 10.11406/rinketsu.59.703.

Abstract

The accepted therapeutic strategy for treating paroxysmal nocturnal hemoglobinuria (PNH) has drastically changed since eculizumab was introduced in 2010 in Japan. Its clinical impact has paved way for the new area of anti-complement therapy, and it has sparked further research and development of anti-complement drugs. The long-term safety and efficacy of eculizumab was established in clinical settings by analyzing post-marketing surveillance that is mandatory in Japan and in clinical trial settings. However, new clinical complications such as resistance to eculizumab, breakthrough hemolysis, extravascular hemolysis, and invasive meningococcal disease (IMD) have emerged after the introduction of eculizumab. Therefore, it is important to strategize effective ways to tackle these issues occurring during eculizumab treatment. In Japan, it is an urgent priority to reach a consensus for managing IMD in patients treated with eculizumab and for establishing protocols for prophylaxis to prevent meningococcal infection.

摘要

自2010年依库珠单抗在日本上市以来,阵发性夜间血红蛋白尿(PNH)的公认治疗策略发生了巨大变化。其临床影响为抗补体治疗这一新领域铺平了道路,并引发了抗补体药物的进一步研发。依库珠单抗的长期安全性和有效性是通过分析日本强制要求的上市后监测以及临床试验数据在临床环境中确立的。然而,依库珠单抗上市后出现了新的临床并发症,如对依库珠单抗耐药、突破性溶血、血管外溶血和侵袭性脑膜炎球菌病(IMD)。因此,制定有效方法来应对依库珠单抗治疗期间出现的这些问题非常重要。在日本,当务之急是就依库珠单抗治疗患者的IMD管理达成共识,并制定预防脑膜炎球菌感染的预防方案。

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