长期使用生物制剂治疗重症哮喘的临床缓解情况

Bradley E. Chipps MD , Njira Lugogo MD , Warner Carr MD , Wenjiong Zhou PhD , Arpan Patel PharmD , Donna D. Carstens MD , Frank Trudo MD, MBA , Christopher S. Ambrose MD, MBA
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引用次数: 0

摘要

背景描述通过长期生物制剂治疗达到临床缓解的重症哮喘(SA)患者比例的真实世界数据非常有限。方法CHRONICLE 是一项针对美国接受亚专科治疗的重症哮喘成人患者的观察性研究。研究机构报告了入组前 12 个月的病情加重情况和生物制剂的使用情况。研究收集了每月的哮喘控制测试评分和专家对哮喘控制的 6 个月评估。对 2018 年 2 月至 2023 年 2 月入组、在研究观察期内开始服用生物制剂并持续使用该生物制剂至少 12 个月的患者进行了评估。在12个月的间隔期内,治疗中出现的临床缓解被定义为没有病情加重和使用全身性皮质类固醇、最近6个月内哮喘控制测试评分提高了50%或更多,至少达到20分,以及专家报告的哮喘控制情况。结果在可评估的患者(n = 611)中,使用生物制剂的中位持续时间为39.6个月。在研究期间的至少一个 12 个月间隔中,79.9% 的患者没有病情加重或使用过全身性皮质类固醇,46.0% 的患者在任何时候都符合临床缓解的定义。临床缓解的点患病率从使用生物制剂 12 到 13 个月时的 22.3% 增加到使用生物制剂 47 到 48 个月时的 34.3%。通过至少1年的生物制剂治疗,临床缓解是SA可行的治疗目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On-treatment clinical remission of severe asthma with real-world longer-term biologic use

Background

There are limited real-world data describing the proportion of patients with severe asthma (SA) who achieve on-treatment clinical remission with long-term biologic treatment.

Objective

Our aim was to examine the proportion and characteristics of adults with SA who achieved clinical remission with biologic therapy.

Methods

CHRONICLE is an observational study of US subspecialist–treated adults with SA. Sites reported exacerbations and biologic use from 12 months before enrollment forward. Monthly Asthma Control Test scores and 6-monthly specialist assessments of asthma control were collected. Patients who enrolled from February 2018 to February 2023, began taking a biologic during the study observation period, and continued use of that biologic for at least 12 months were evaluated. Incident on-treatment clinical remission was defined in a 12-month interval as the absence of exacerbations and systemic corticosteroid use, a 50% or greater improvement in Asthma Control Test scores of least 20 points in the latest 6 months, and specialist report of asthma control.

Results

Among the evaluable patients (n = 611), the median duration of biologic use was 39.6 months. In at least one 12-month interval during the study, 79.9% of patients had no exacerbations or systemic corticosteroid use and 46.0% met the definition of clinical remission at any point. The point prevalence of clinical remission increased from 22.3% at 12 to 13 months of biologic use to 34.3% at 47 to 48 months of biologic use.

Conclusions

In a real-world cohort of patients with SA with longer-term biologic treatment, almost one-half achieved on-treatment clinical remission. With at least 1 year of biologic therapy, clinical remission is a feasible treatment goal in SA.
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来源期刊
The journal of allergy and clinical immunology. Global
The journal of allergy and clinical immunology. Global Immunology, Allergology and Rheumatology
CiteScore
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审稿时长
92 days
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