European Respiratory Journal ( IF 16.6 ) Pub Date : 2024-08-22 , DOI: 10.1183/13993003.00404-2024 Marianne Baastrup Soendergaard 1 , Anne-Sofie Bjerrum 2 , Linda Makowska Rasmussen 3 , Sofie Lock-Johansson 4 , Ole Hilberg 5 , Susanne Hansen 6, 7 , Anna von Bulow 6 , Celeste Porsbjerg 6
The treatment of severe eosinophilic asthma has been revolutionised with the introduction of anti-interleukin (IL)-5 biological treatment. Anti-IL-5 biologics include mepolizumab, benralizumab and reslizumab, all of which target the IL-5 pathway; regulatory randomised controlled trials (RCTs) have shown that they are efficient in reducing exacerbation rates and the need for maintenance oral corticosteroids (mOCS) [1–6]. Real-life results from the use of anti-IL-5 biologics suggest that they have exceeded the expectations set by RCTs. Data from the nationwide Danish Severe Asthma Register (DSAR) showed that 58% of patients achieved a complete response with complete abrogation of the outcomes that set the indication for treatment: exacerbations and need for mOCS [7].
中文翻译:
严重哮喘中抗 IL-5 生物制剂的滴定:一项开放标签随机对照试验(OPTIMAL 研究)
随着抗白细胞介素 (IL)-5 生物治疗的引入,严重嗜酸性粒细胞性哮喘的治疗发生了革命性的变化。抗 IL-5 生物制剂包括美泊利单抗、贝那利珠单抗和瑞利珠单抗,它们都靶向 IL-5 通路;监管性随机对照试验 (RCT) 表明,它们在降低急性加重率和维持口服皮质类固醇 (mOCS) 的需求方面有效 [1-6]。使用抗 IL-5 生物制剂的真实结果表明,它们已经超出了 RCT 设定的预期。来自全国丹麦严重哮喘登记册 (DSAR) 的数据显示,58% 的患者获得了完全缓解,完全消除了设定治疗适应证的结局:恶化和需要 mOCS [7]。