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美泊利单抗和贝那利珠单抗治疗重度嗜酸性粒细胞性哮喘及嗜酸性肉芽肿性多血管炎的“超级应答者”的真实世界特征

Real-world characteristics of "super-responders" to mepolizumab and benralizumab in severe eosinophilic asthma and eosinophilic granulomatosis with polyangiitis.

作者信息

Portacci Andrea, Campisi Raffaele, Buonamico Enrico, Nolasco Santi, Pelaia Corrado, Crimi Nunzio, Benfante Alida, Triggiani Massimo, Spadaro Giuseppe, Caiaffa Maria Filomena, Scioscia Giulia, Detoraki Aikaterini, Valenti Giuseppe, Papia Francesco, Tomasello Alessandra, Scichilone Nicola, Pelaia Girolamo, Crimi Claudia, Carpagnano Giovanna Elisiana

机构信息

Institute of Respiratory Disease, Department of Translational Biomedicine and Neuroscience, University "Aldo Moro", Bari, Italy.

These authors contributed equally.

出版信息

ERJ Open Res. 2023 Oct 30;9(5). doi: 10.1183/23120541.00419-2023. eCollection 2023 Sep.

Abstract

BACKGROUND

The current definition of severe eosinophilic asthma (SEA) super-responders to biologic treatment does not include patients with other eosinophil-based comorbidities. Although eosinophilic granulomatosis with polyangiitis (EGPA) is frequently associated with SEA, we lack data on a possible super-response to biologic treatments in patients suffering from these two diseases. We aim to assess super-responder features in real-life patients with SEA and EGPA treated with mepolizumab and benralizumab.

METHODS

We enrolled 39 patients with SEA and EGPA eligible for treatment with mepolizumab or benralizumab. Super-responder assessment was performed considering oral corticosteroid (OCS) cessation, lack of exacerbations, forced expiratory volume in 1 s and Asthma Control Test (ACT) improvement.

RESULTS

Super-responders showed worse clinical baseline characteristics than non-super-responder patients, with a greater improvement in severe asthma exacerbations, OCS dose reduction and ACT score increase. Definition of super-responders was consistent only considering a 12-month course of monoclonal antibody, lacking sensitivity in earlier evaluations.

CONCLUSION

Mepolizumab and benralizumab are safe and effective in patients with EGPA and SEA, since a consistent proportion of patients show a super-response after 12 months of treatment. Further studies will address specific criteria for super-responder assessment in these patients.

摘要

背景

目前严重嗜酸性粒细胞性哮喘(SEA)生物治疗超级应答者的定义不包括患有其他嗜酸性粒细胞相关合并症的患者。虽然嗜酸性粒细胞肉芽肿性多血管炎(EGPA)常与SEA相关,但我们缺乏关于这两种疾病患者对生物治疗可能出现超级应答的数据。我们旨在评估接受美泊利珠单抗和贝那利珠单抗治疗的现实生活中SEA和EGPA患者的超级应答者特征。

方法

我们纳入了39例符合美泊利珠单抗或贝那利珠单抗治疗条件的SEA和EGPA患者。超级应答者评估通过考虑口服糖皮质激素(OCS)停用、无加重发作、1秒用力呼气量和哮喘控制测试(ACT)改善情况来进行。

结果

超级应答者的临床基线特征比非超级应答者更差,但在严重哮喘发作、OCS剂量减少和ACT评分增加方面有更大改善。仅考虑单克隆抗体12个月疗程时超级应答者的定义是一致的,在早期评估中缺乏敏感性。

结论

美泊利珠单抗和贝那利珠单抗对EGPA和SEA患者安全有效,因为相当比例的患者在治疗12个月后显示出超级应答。进一步的研究将探讨这些患者超级应答者评估的具体标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7989/10613971/130336886dc0/00419-2023.01.jpg

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