Eculizumab as Additional Rescue Therapy in Myasthenic Crisis

Muscles Pub Date : 2024-02-07 DOI:10.3390/muscles3010005
F. Crescenzo, Mattia Zanoni, Laura Ferigo, Francesca Rossi, Matteo Grecò, Angelica Lupato, Alessandra Danese, Domenico Ajena, Michelangelo Turazzini
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Abstract

Eculizumab is a monoclonal antibody blocking the terminal complement protein C5. As demonstrated in the phase III randomized, placebo-controlled, REGAIN clinical trial, eculizumab is efficacious in acetylcholine receptor antibody (AChR-Ab)-positive refractory generalized myasthenia gravis (gMG) (Myasthenia Gravis Foundation of America—MGFA class II–IV). It has not been studied in severe myasthenic exacerbation or myasthenic crisis (MGFA V). A 73-year-old man diagnosed with myasthenia gravis AChR-Ab positivity came to our observation for symptoms of bulbar and ocular weakness and unresponsiveness or intolerability to conventional immunosuppressive therapies (prednisone and azathioprine). Due to the recurrent clinical worsening with intubation over a short-term period, the patient was treated with eculizumab. After 15 days of eculizumab treatment, we observed a significant recovery of clinical condition. We discharged the patient to an outpatient regimen, where he is continuing with maintenance doses of eculizumab and slowly tapering steroid intake. The use of eculizumab in myasthenic crises is still anecdotal. Our case aims to provide eculizumab benefit for refractory severe gMG in a practical, real-world setting beyond the criteria of the REGAIN study. Further studies are needed to evaluate the efficacy and safety of eculizumab in myasthenic crises.
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将依库珠单抗作为肌无力危象的额外救援疗法
Eculizumab 是一种阻断末端补体蛋白 C5 的单克隆抗体。REGAIN III 期随机安慰剂对照临床试验表明,依库珠单抗对乙酰胆碱受体抗体(AChR-Ab)阳性的难治性全身性重症肌无力(gMG)(美国重症肌无力基金会-MGFA II-IV 级)有效。目前尚未对重症肌无力加重或肌无力危象(MGFA V 级)进行研究。一名被诊断为肌无力 AChR-Ab 阳性的 73 岁男子因出现球部和眼部无力症状,以及对常规免疫抑制疗法(强的松和硫唑嘌呤)无反应或无法耐受而前来就诊。由于患者的临床症状在短期内反复恶化,需要插管治疗,因此我们使用了依库珠单抗。在接受 15 天的依库珠单抗治疗后,我们观察到患者的临床状况明显好转。患者出院后,我们对其进行了门诊治疗,继续使用维持剂量的依库珠单抗,并缓慢减少类固醇的摄入量。在肌无力危象中使用依库珠单抗仍是传闻。我们的病例旨在超越 REGAIN 研究的标准,在实际的现实环境中为难治性重症肌无力患者提供依库珠单抗的益处。还需要进一步研究来评估依库珠单抗在肌无力危象中的疗效和安全性。
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