Mayo Clinic School of Graduate Medical Education, Mayo Clinic-Rochester, 200 First Street SW, Rochester, MN, 55905, USA.
Department of Pediatrics, Mayo Clinic-Rochester, Rochester, MN, USA.
Lung. 2020 Aug;198(4):653-659. doi: 10.1007/s00408-020-00369-8. Epub 2020 Jun 24.
To determine the efficacy of IL-5 inhibitory therapy in severe, refractory asthma in a real-world clinical setting from a tertiary referral center.
A retrospective chart review of patients with severe asthma treated with IL-5 biologic therapy for ≥ 6 months at Mayo Clinic in Rochester, Minnesota between January 1, 2013 and August 31, 2019.
Over the study period, we identified 63 patients with a mean age of 54 who received an IL-5 inhibitor for ≥ 6 months. A total of 55 patients received mepolizumab, 2 received benralizumab, and 9 patients received both. Patients were followed up for a mean of 25 months. The mean number of months of oral prednisone use prior to biologic initiation was 64. There was a significant reduction in the median dose of prednisone in the 24 months after drug initiation (15 mg vs. 0 mg; p = < 0.0001). Similarly; there was a significant decline in the median number of asthma exacerbations in the 24 months before and after drug initiation (7 vs. 2; p = < 0.0001). The mean number of emergency room (ER) visits and hospitalizations decreased from 5.1 and 2.0 to 1.6 and 0.4 in the 24 months before and after therapy initiation (p < 0.0001 and p = 0.007, respectively) CONCLUSIONS: IL-5 inhibitory therapy is associated with significant and long-term sustained reductions in asthma exacerbation frequency, ER visits, hospitalizations, as well as oral steroid usage in a patient population with refractory steroid-dependent asthma referred to a tertiary referral center.
在明尼苏达州罗切斯特市梅奥诊所的三级转诊中心的真实临床环境中,确定 IL-5 抑制疗法在重度、难治性哮喘中的疗效。
对 2013 年 1 月 1 日至 2019 年 8 月 31 日期间在明尼苏达州罗切斯特市梅奥诊所接受 IL-5 生物治疗治疗时间≥6 个月的重度哮喘患者进行回顾性图表审查。
在研究期间,我们确定了 63 名平均年龄为 54 岁的患者,他们接受了 IL-5 抑制剂治疗时间≥6 个月。共有 55 名患者接受了美泊利珠单抗治疗,2 名患者接受了贝那利珠单抗治疗,9 名患者同时接受了两种药物治疗。患者的平均随访时间为 25 个月。在开始使用生物制剂前,口服泼尼松的平均时间为 64 个月。在药物开始后 24 个月内,泼尼松的中位剂量显著降低(15mg 与 0mg;p<0.0001)。同样,在药物开始前和开始后 24 个月内,哮喘加重的中位次数也显著下降(7 次与 2 次;p<0.0001)。在开始治疗前和开始治疗后的 24 个月内,急诊室(ER)就诊次数和住院次数的平均值分别从 5.1 次和 2.0 次减少到 1.6 次和 0.4 次(p<0.0001 和 p=0.007,分别)。
在转诊至三级转诊中心的难治性类固醇依赖型哮喘患者中,IL-5 抑制疗法与哮喘加重频率、急诊室就诊次数、住院次数以及口服类固醇使用率的显著且长期持续降低相关。