Chipps Bradley E, Lugogo Njira, Carr Warner, Zhou Wenjiong, Patel Arpan, Carstens Donna D, Trudo Frank, Ambrose Christopher S
Capital Allergy and Respiratory Disease Center, Sacramento, Calif.
University of Michigan, Ann Arbor, Mich.
J Allergy Clin Immunol Glob. 2024 Oct 30;4(1):100365. doi: 10.1016/j.jacig.2024.100365. eCollection 2025 Feb.
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.
Our aim was to examine the proportion and characteristics of adults with SA who achieved clinical remission with biologic therapy.
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.
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.
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.
描述重度哮喘(SA)患者通过长期生物治疗实现治疗期临床缓解比例的真实世界数据有限。
我们的目的是研究通过生物治疗实现临床缓解的成年SA患者的比例及特征。
CHRONICLE是一项针对美国专科医生治疗的成年SA患者的观察性研究。各研究点报告了入组前12个月起的病情加重情况和生物制剂使用情况。收集每月哮喘控制测试分数以及每6个月对哮喘控制情况进行的专科评估结果。对2018年2月至2023年2月入组、在研究观察期开始使用生物制剂并持续使用该生物制剂至少12个月的患者进行评估。治疗期临床缓解定义为在12个月期间无病情加重且未使用全身糖皮质激素、哮喘控制测试分数提高50%或更多(最近6个月内至少提高20分)以及专科医生报告哮喘得到控制。
在可评估患者(n = 611)中,生物制剂使用的中位时长为39.6个月。在研究期间至少一个12个月期间,79.9%的患者无病情加重或未使用全身糖皮质激素,46.0%的患者在任何时间点符合临床缓解定义。临床缓解的时点患病率从生物制剂使用12至13个月时的22.3%增至生物制剂使用47至48个月时的34.3%。
在接受长期生物治疗的SA患者真实世界队列中,近一半患者实现了治疗期临床缓解。进行至少1年的生物治疗后,临床缓解是SA可行的治疗目标。