Clinical remission and control in severe asthma: agreements and disagreements.

Q2 Pharmacology, Toxicology and Pharmaceutics
Drugs in Context Pub Date : 2024-09-23 eCollection Date: 2024-01-01 DOI:10.7573/dic.2024-7-2
Annamaria Bosi, Carlo Lombardi, Cristiano Caruso, Marcello Cottini, Ilaria Baglivo, Stefania Colantuono, Francesco Menzella
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引用次数: 0

Abstract

Over the last two decades, we have witnessed great advancements in our understanding of the immunological pathways of asthma, leading to the development of targeted therapies, such as biologic drugs, that have radically and definitively changed the clinical outcomes of severe asthma. Despite the numerous therapeutic options available, ~4-10% of all people with asthma have severe or uncontrolled asthma, associated with an increased risk of developing chronic oral corticosteroid use, fixed airflow limitation, exacerbations, hospitalization and, finally, increased healthcare costs. The new concept of disease modification in asthma comes from the evolution of asthma management, which encompasses phenotyping patients with different inflammatory endotypes characterizing the disease, followed by the advent of more effective therapies capable of targeting the proximal factors of airway inflammation. This treat-to-target approach aims to achieve remission of the disease. Because the novel treatment paradigm for severe asthma with the advent of biologic therapies is no longer clinical control but rather clinical remission - a step closer to the concept of cure - a deeper and more accurate understanding of the critical causal mechanisms and endotypes of asthma is necessary to achieve the goal of clinical remission, which has the potential to generate real life-changing benefits for patients. This review aims to frame the evolution of the debated concept of clinical remission and provide clinicians with insights that may be helpful in achieving remission in the greatest number of patients.

严重哮喘的临床缓解与控制:共识与分歧。
在过去二十年里,我们对哮喘免疫途径的认识取得了巨大进步,从而开发出了生物药物等靶向疗法,彻底改变了重症哮喘的临床治疗效果。尽管治疗方法众多,但仍有约 4-10% 的哮喘患者患有严重或无法控制的哮喘,这与长期口服皮质类固醇、固定气流受限、病情加重、住院以及医疗费用增加的风险有关。哮喘疾病调整的新概念源于哮喘治疗的演变,其中包括对具有不同炎症内型特征的患者进行表型分析,随后出现了能够针对气道炎症近端因素的更有效疗法。这种 "靶向治疗 "方法旨在实现疾病的缓解。由于随着生物疗法的出现,重症哮喘的新治疗模式不再是临床控制,而是临床缓解--更接近治愈的概念--因此必须更深入、更准确地了解哮喘的关键致病机制和终末型,才能实现临床缓解的目标,这有可能为患者带来真正改变生活的益处。这篇综述旨在勾勒出临床缓解这一备受争议的概念的演变过程,并为临床医生提供可能有助于使更多患者获得缓解的真知灼见。
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
Drugs in Context
Drugs in Context Medicine-Medicine (all)
CiteScore
5.90
自引率
0.00%
发文量
63
审稿时长
9 weeks
期刊介绍: Covers all phases of original research: laboratory, animal and human/clinical studies, health economics and outcomes research, and postmarketing studies. Original research that shows positive or negative results are welcomed. Invited review articles may cover single-drug reviews, drug class reviews, latest advances in drug therapy, therapeutic-area reviews, place-in-therapy reviews, new pathways and classes of drugs. In addition, systematic reviews and meta-analyses are welcomed and may be published as original research if performed per accepted guidelines. Editorials of key topics and issues in drugs and therapeutics are welcomed. The Editor-in-Chief will also consider manuscripts of interest in areas such as technologies that support diagnosis, assessment and treatment. EQUATOR Network reporting guidelines should be followed for each article type. GPP3 Guidelines should be followed for any industry-sponsored manuscripts. Other Editorial sections may include Editorial, Case Report, Conference Report, Letter-to-the-Editor, Educational Section.
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