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可治疗特征导向的哮喘管理:一项可行性研究。

Treatable Trait Guided Asthma Management: A Feasibility Study.

作者信息

Fingleton James, McLachlan Rob, Sparks Jenny, Beasley Richard, Agustí Alvar, Gibson Peter G, Pavord Ian D, Hardy Jo, Weatherall Mark, Eathorne Allie, McDonald Vanessa M

机构信息

Te Whatu Ora - Capital, Coast and Hutt Valley, Wellington, New Zealand.

Medical Research Institute of New Zealand, Wellington, New Zealand.

出版信息

Respirology. 2025 Jun;30(6):480-492. doi: 10.1111/resp.70016. Epub 2025 Mar 12.

Abstract

BACKGROUND AND OBJECTIVES

Treatable trait-based personalised medicine improves outcomes in severe asthma clinics. We assessed the feasibility of a randomised controlled trial (RCT) of protocolised treatable trait-guided asthma management in patients not under a severe asthma clinic.

METHODS

Ten week single-group cohort study. Participants had a doctor's diagnosis of asthma, Asthma Control Questionnaire-5 (ACQ-5) score > 1, and ≥ 1 exacerbation in the last year.

INTERVENTION

biomarker-guided asthma medication according to a protocolised algorithm, targeting traits of type-2 inflammation and airflow obstruction. Feasibility outcomes: recruitment rates, acceptability of intervention, willingness to enrol in an RCT, need for 'extended' trait assessment after 10 weeks, and estimation of trait prevalence.

RESULTS

Recruitment ceased with 29/50 participants after 14 months due to difficulties associated with COVID-19. Recruitment rate: 29/118 (25%) of those invited to participate (95% CI 17 to 33). 24/26 (92%) participants found the intervention acceptable and were willing to participate in a future study. After 10 weeks, 65% remained not well controlled (ACQ-5 > 1) and would have required the 'extended' assessment. Participants had a mean (SD) 4.8 (2.3) of 13 traits assessed. ACQ-5 improved during the study by -1.0 (0.3 to 1.8) units, and post-bronchodilator airflow limitation reduced from 59% of participants to 35%. 12/29 (41%) participants received continuous oral corticosteroids at some point during the study.

CONCLUSION

Protocolised treatable trait management was acceptable to participants, associated with significant clinical benefit, and a full RCT appears feasible. Targeting type-2 inflammation and airflow obstruction was insufficient to control asthma in the majority of patients, despite marked systemic corticosteroid exposure.

TRIAL REGISTRATION

ACTRN12620000935932.

摘要

背景与目的

基于可治疗特征的个性化医疗可改善重度哮喘诊所的治疗效果。我们评估了在非重度哮喘诊所的患者中开展一项随机对照试验(RCT)的可行性,该试验采用规范化的、基于可治疗特征的哮喘管理方案。

方法

为期10周的单组队列研究。参与者经医生诊断为哮喘,哮喘控制问卷-5(ACQ-5)评分>1,且在过去一年中至少有1次病情加重。

干预措施

根据规范化算法进行生物标志物指导的哮喘药物治疗,针对2型炎症和气流受限的特征。可行性结果:招募率、干预措施的可接受性、参与RCT的意愿、10周后进行“扩展”特征评估的必要性以及特征患病率的估计。

结果

由于与COVID-19相关的困难,14个月后招募了29/50名参与者,招募工作停止。招募率:受邀参与的人员中有29/118(25%)参与(95%CI 17至33)。24/26(92%)的参与者认为干预措施可接受,并愿意参与未来的研究。10周后,65%的患者仍未得到良好控制(ACQ-5>1),需要进行“扩展”评估。参与者平均(标准差)评估了13项特征中的4.8(2.3)项。在研究期间,ACQ-5改善了-1.0(0.3至1.8)个单位,支气管扩张剂后气流受限从59%的参与者降至35%。12/29(41%)的参与者在研究期间的某个时间点接受了持续口服糖皮质激素治疗。

结论

规范化的可治疗特征管理为参与者所接受,具有显著的临床益处,全面的RCT似乎是可行的。尽管全身糖皮质激素暴露显著,但针对2型炎症和气流受限不足以控制大多数患者的哮喘。

试验注册

ACTRN12620000935932。

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