Suppr超能文献

美泊利单抗在过敏性和非过敏性哮喘患者中的真实世界疗效

Real-World Effectiveness of Mepolizumab in Patients with Allergic and Non-Allergic Asthma.

作者信息

Silver Jared, Steffens Andrea, Chastek Benjamin, Deb Arijita

机构信息

Medical Affairs, GSK, Durham, NC, USA.

Optum, Eden Prairie, MN, USA.

出版信息

J Asthma Allergy. 2024 Mar 23;17:261-271. doi: 10.2147/JAA.S444693. eCollection 2024.

Abstract

PURPOSE

Real-world data on mepolizumab in patients with severe asthma and allergic and non-allergic phenotypes are limited. This study investigated the effectiveness of mepolizumab treatment in patients with severe asthma with allergic and non-allergic phenotypes.

PATIENTS AND METHODS

This retrospective cohort study (GSK ID: 214148) used administrative claims data from the Optum Research Database. Eligible patients were ≥6 years of age with asthma and had ≥2 mepolizumab claims post-index. Index date was the first mepolizumab claim/administration (January 2016-December 2018). Patients were divided into two cohorts: allergic and non-allergic asthma, based on diagnosis codes, medication use and lab test results. Outcomes included the rate of asthma-related exacerbations and oral corticosteroid (OCS) use during the 12 months before (baseline period) and 12 months after (follow-up period) mepolizumab initiation. Study ended in December 2019.

RESULTS

Overall, 240 (44.6%) and 298 (55.4%) patients were included in the allergic and non-allergic asthma cohorts, respectively. Mean (standard deviation [SD]) counts of asthma-related exacerbations were significantly reduced from baseline to follow-up in both the allergic and non-allergic asthma cohorts (3.2 [2.5] to 2.1 [2.1], p < 0.001 and 2.5 [2.2] to 1.7 [1.9], p < 0.001, respectively). The mean number of OCS pharmacy claims was significantly decreased by 33.3% and 41.4% from baseline to follow-up in the allergic and non-allergic cohorts, respectively (p < 0.001); mean daily OCS dose significantly decreased by 30.6% and 45.4%, respectively (p < 0.001) as well as the mean number of OCS bursts, which decreased by 44.9% and 41.8%, respectively (p < 0.001). No significant differences were observed between cohorts in reductions in asthma exacerbations, counts of OCS pharmacy claims or OCS bursts (baseline to follow-up).

CONCLUSION

Mepolizumab significantly reduced asthma exacerbations and OCS use in patients with allergic and non-allergic asthma, suggesting that mepolizumab provides real-world benefit in severe asthma irrespective of whether a patient has an allergic phenotype.

摘要

目的

关于美泊利珠单抗治疗重度哮喘以及过敏和非过敏表型患者的真实世界数据有限。本研究调查了美泊利珠单抗治疗重度哮喘过敏和非过敏表型患者的有效性。

患者与方法

这项回顾性队列研究(葛兰素史克编号:214148)使用了Optum研究数据库中的管理索赔数据。符合条件的患者年龄≥6岁,患有哮喘,且索引后有≥2次美泊利珠单抗索赔记录。索引日期为首次美泊利珠单抗索赔/给药日期(2016年1月 - 2018年12月)。根据诊断代码、药物使用和实验室检查结果,将患者分为两个队列:过敏性哮喘和非过敏性哮喘。结局指标包括美泊利珠单抗开始使用前12个月(基线期)和开始使用后12个月(随访期)内哮喘相关加重的发生率以及口服糖皮质激素(OCS)的使用情况。研究于2019年12月结束。

结果

总体而言,过敏性哮喘队列和非过敏性哮喘队列分别纳入了240例(44.6%)和298例(55.4%)患者。过敏性哮喘队列和非过敏性哮喘队列中,从基线到随访,哮喘相关加重的平均(标准差[SD])次数均显著减少(分别从3.2[2.5]降至2.1[2.1],p<0.001;从2.5[2.2]降至1.7[1.9],p<0.001)。从基线到随访,过敏性队列和非过敏性队列中OCS药房索赔的平均次数分别显著减少33.3%和41.4%(p<0.001);OCS平均每日剂量分别显著减少30.6%和45.4%(p<0.001),OCS冲击次数平均也分别减少44.9%和41.8%(p<0.001)。两个队列在哮喘加重减少、OCS药房索赔次数或OCS冲击次数(从基线到随访)方面未观察到显著差异。

结论

美泊利珠单抗显著减少了过敏性和非过敏性哮喘患者的哮喘加重及OCS使用,这表明无论患者是否具有过敏表型,美泊利珠单抗在重度哮喘中都具有真实世界的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14b3/10967551/c306bc984469/JAA-17-261-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验