Biologics in severe asthma: a state-of-the-art review.

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM
European Respiratory Review Pub Date : 2025-01-08 Print Date: 2025-01-01 DOI:10.1183/16000617.0088-2024
Bishal Gyawali, Steve N Georas, Sandhya Khurana
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引用次数: 0

Abstract

Asthma is considered severe if it remains uncontrolled despite optimal conventional therapy, characterised by poor symptom control, frequent exacerbations and increased exposure to systemic corticosteroids. This has a significant impact on morbidity, mortality and healthcare resource utilisation. Recent advances in the understanding of asthma heterogeneity and immunopathogenesis have helped delineate precise disease pathways. The discovery of these pivotal pathways has led to the development of highly effective biologic therapies. Currently available asthma biologics target immunoglobulin E, interleukin (IL)-5/IL-5Rα, IL-4Rα and thymic stromal lymphopoietin. Identification of specific asthma phenotypes, utilising easily measurable biomarkers, has paved the way towards personalised and precision asthma management. Biologic therapies play a significant role in reducing exacerbations, hospitalisations and the need for maintenance systemic steroids, while also improving the quality of life in patients with severe asthma. The evidence for their clinical efficacy comes from randomised controlled trials (RCTs), extension studies, metanalyses and real-world data. This review synthesises findings from early, pivotal RCTs and subsequent studies following the approval of biologics for severe asthma. The safety and efficacy data from these studies, completed in a variety of settings, provide practical perspectives on their application and enhance their generalisability.

重度哮喘中的生物制剂:最新进展综述。
如果哮喘在最佳常规治疗后仍不受控制,则被认为是严重的,其特征是症状控制不佳、频繁恶化和全身皮质类固醇暴露增加。这对发病率、死亡率和保健资源的利用产生了重大影响。最近在了解哮喘异质性和免疫发病机制方面的进展有助于描述精确的疾病途径。这些关键途径的发现导致了高效生物疗法的发展。目前可用的哮喘生物制剂靶向免疫球蛋白E、白细胞介素(IL)-5/IL- 5r α、IL- 4r α和胸腺基质淋巴生成素。利用易于测量的生物标志物识别特定的哮喘表型,为个性化和精确的哮喘管理铺平了道路。生物疗法在减少病情恶化、住院和维持全身性类固醇方面发挥着重要作用,同时也改善了严重哮喘患者的生活质量。其临床疗效的证据来自随机对照试验(rct)、扩展研究、元分析和真实世界的数据。本综述综合了重症哮喘生物制剂获批后早期关键性随机对照试验和后续研究的结果。在各种环境下完成的这些研究的安全性和有效性数据为它们的应用提供了实际的视角,并增强了它们的普遍性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Respiratory Review
European Respiratory Review Medicine-Pulmonary and Respiratory Medicine
CiteScore
14.40
自引率
1.30%
发文量
91
审稿时长
24 weeks
期刊介绍: The European Respiratory Review (ERR) is an open-access journal published by the European Respiratory Society (ERS), serving as a vital resource for respiratory professionals by delivering updates on medicine, science, and surgery in the field. ERR features state-of-the-art review articles, editorials, correspondence, and summaries of recent research findings and studies covering a wide range of topics including COPD, asthma, pulmonary hypertension, interstitial lung disease, lung cancer, tuberculosis, and pulmonary infections. Articles are published continuously and compiled into quarterly issues within a single annual volume.
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