治疗冷凝集素病的 Sutimlimab。

Mark Reid, Bethany A Fedutes Henderson
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引用次数: 0

摘要

冷凝集素病(CAD)是一种罕见的自身免疫性溶血性贫血(AIHA),有别于温抗体型 AIHA。区别之一在于,与温抗体型自身免疫性溶血性贫血相比,冷凝集素病通常对皮质类固醇无反应。一直以来,CAD 的治疗方法仅限于免疫疗法或化学免疫疗法,但疗效各异。冷凝集素病还存在血栓形成和死亡的风险。对患者来说,疲劳往往是 CAD 的常见症状。CAD的特征是补体介导的溶血,这使得补体抑制剂成为患者的重要治疗选择。以前,C5 抑制剂 eculizumab 对 CAD 的治疗效果有限。最近,C1s 抑制剂 sutimlimab 在两项 III 期研究中被证明是治疗 CAD 的有效药物,可改善血红蛋白、溶血和疲劳。然而,有关 CAD,特别是有关 sutimlimab 的医学文献却很少,而且这些文献都是针对高级医疗人员 (APP) 的。这篇文章旨在为医生提供有关 CAD 的背景知识,并重点介绍 sutimlimab,以帮助他们护理接受这种疗法的 CAD 患者。
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Sutimlimab for Cold Agglutinin Disease.

Cold agglutinin disease (CAD) is a rare type of autoimmune hemolytic anemia (AIHA) distinct from warm antibody AIHA. One of the ways it is distinct is that CAD is usually not responsive to corticosteroids compared with warm antibody AIHA. Historically, CAD therapy has been limited to immunotherapy or chemoimmunotherapy with varying responses. Cold agglutinin disease also poses a risk for thrombosis and mortality. For patients, fatigue tends to be a common symptom of CAD. The hallmark of CAD is complement-mediated hemolysis, which makes complement inhibitors a critical therapeutic option for patients. Previously, eculizumab, a C5 inhibitor, had limited therapeutic effect for CAD. More recently, sutimlimab, a C1s inhibitor, was shown in two phase III studies to be an efficacious treatment for CAD, improving hemoglobin, hemolysis, and fatigue. However, there is a paucity of medical literature on CAD and on sutimlimab in particular that is geared toward advanced practice providers (APPs). This article aims to provide APPs with a background in CAD and a focus on sutimlimab, assisting these providers in caring for patients with CAD receiving this therapy.

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