Advancing COPD management through novel pharmacological agents: ensifentrine and dupilumab.

IF 4.5 Q2 RESPIRATORY SYSTEM
Breathe Pub Date : 2025-12-16 eCollection Date: 2025-10-01 DOI:10.1183/20734735.0206-2025
Lauren L Walkon, James R Burmeister, Michael Nazmifar, Forrest Bohler, Anna Kochanowska-Karamyan, Samuel A Allen
{"title":"Advancing COPD management through novel pharmacological agents: ensifentrine and dupilumab.","authors":"Lauren L Walkon, James R Burmeister, Michael Nazmifar, Forrest Bohler, Anna Kochanowska-Karamyan, Samuel A Allen","doi":"10.1183/20734735.0206-2025","DOIUrl":null,"url":null,"abstract":"<p><p>COPD is a progressive respiratory condition characterised by persistent airflow limitation and chronic inflammation. Despite advances in bronchodilator and corticosteroid therapy, many patients, particularly those with eosinophilic inflammation, remain inadequately managed. This review highlights two recently approved therapies, ensifentrine and dupilumab, which represent a shift toward precision medicine in COPD management. Ensifentrine, a dual phosphodiesterase 3 and 4 inhibitor, offers both bronchodilatory and anti-inflammatory effects, improving lung function and reducing exacerbations. Dupilumab targets interleukin-4 and interleukin-13 signalling, addressing type 2 inflammatory pathways prominent in eosinophilic COPD. Key clinical trials (ENHANCE, BOREAS, NOTUS) demonstrate the efficacy of these agents in improving forced expiratory volume in 1 s, reducing exacerbation rates, and enhancing quality of life in select patient subgroups. By focusing on disease endotypes, these novel therapies underscore the growing role of personalised treatment approaches in COPD. Continued investigation into biomarkers and long-term outcomes will be essential for integrating these therapies into routine clinical practice.</p>","PeriodicalId":9292,"journal":{"name":"Breathe","volume":"21 4","pages":"250206"},"PeriodicalIF":4.5000,"publicationDate":"2025-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12706593/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Breathe","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1183/20734735.0206-2025","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0

Abstract

COPD is a progressive respiratory condition characterised by persistent airflow limitation and chronic inflammation. Despite advances in bronchodilator and corticosteroid therapy, many patients, particularly those with eosinophilic inflammation, remain inadequately managed. This review highlights two recently approved therapies, ensifentrine and dupilumab, which represent a shift toward precision medicine in COPD management. Ensifentrine, a dual phosphodiesterase 3 and 4 inhibitor, offers both bronchodilatory and anti-inflammatory effects, improving lung function and reducing exacerbations. Dupilumab targets interleukin-4 and interleukin-13 signalling, addressing type 2 inflammatory pathways prominent in eosinophilic COPD. Key clinical trials (ENHANCE, BOREAS, NOTUS) demonstrate the efficacy of these agents in improving forced expiratory volume in 1 s, reducing exacerbation rates, and enhancing quality of life in select patient subgroups. By focusing on disease endotypes, these novel therapies underscore the growing role of personalised treatment approaches in COPD. Continued investigation into biomarkers and long-term outcomes will be essential for integrating these therapies into routine clinical practice.

Abstract Image

Abstract Image

Abstract Image

通过新型药物推进COPD治疗:恩西芬汀和杜匹单抗。
慢性阻塞性肺病是一种进行性呼吸系统疾病,其特征是持续气流受限和慢性炎症。尽管支气管扩张剂和皮质类固醇治疗取得了进展,但许多患者,特别是嗜酸性粒细胞炎症患者,仍然没有得到充分的治疗。这篇综述强调了最近批准的两种治疗方法,ensifentrine和dupilumab,它们代表了COPD治疗向精准医学的转变。Ensifentrine是一种双磷酸二酯酶3和4抑制剂,具有支气管扩张和抗炎作用,改善肺功能并减少恶化。Dupilumab靶向白细胞介素-4和白细胞介素-13信号传导,解决嗜酸性COPD中突出的2型炎症途径。关键的临床试验(ENHANCE, BOREAS, NOTUS)证明了这些药物在改善15秒内用力呼气量,降低急性加重率和提高特定患者亚组的生活质量方面的有效性。通过关注疾病的内源性类型,这些新疗法强调了个性化治疗方法在COPD中日益重要的作用。对生物标志物和长期结果的持续研究对于将这些疗法纳入常规临床实践至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Breathe
Breathe RESPIRATORY SYSTEM-
CiteScore
2.90
自引率
5.00%
发文量
51
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书