恩斯芬汀加长效毒蕈碱拮抗剂治疗COPD:三功能双支气管扩张的视角。

IF 14.4 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Drugs Pub Date : 2025-09-01 Epub Date: 2025-07-24 DOI:10.1007/s40265-025-02213-w
Mario Cazzola, Clive P Page, Luigino Calzetta, Fernando J Martinez, Paola Rogliani, Maria Gabriella Matera
{"title":"恩斯芬汀加长效毒蕈碱拮抗剂治疗COPD:三功能双支气管扩张的视角。","authors":"Mario Cazzola, Clive P Page, Luigino Calzetta, Fernando J Martinez, Paola Rogliani, Maria Gabriella Matera","doi":"10.1007/s40265-025-02213-w","DOIUrl":null,"url":null,"abstract":"<p><p>Chronic obstructive pulmonary disease (COPD) management has evolved with the emergence of advanced pharmacological strategies, notably dual bronchodilation and bifunctional agents. Among these innovations, the selective inhaled phosphodiesterase (PDE)3/4 inhibitor ensifentrine represents a novel therapeutic class that combines bronchodilatory and anti-inflammatory properties within a single molecular entity. Dual bronchodilation, traditionally achieved through the combination of long-acting muscarinic antagonists (LAMAs) and long-acting β<sub>2</sub>-agonists, has demonstrated superior efficacy compared with monotherapies, including enhanced pulmonary function, reduced symptom burden, and decreased exacerbation frequency. Ensifentrine, recently approved by the US Food and Drug Administration, exerts bronchodilation via PDE3 inhibition and suppresses inflammation by inhibiting PDE4, offering complementary benefits when combined with LAMAs. Clinical trials, including ENHANCE-1 and ENHANCE-2, have shown that ensifentrine significantly improves FEV<sub>1</sub>, reduces exacerbations, and lowers inflammatory biomarkers, with a favorable safety profile. Notably, preclinical and clinical data suggest synergism between ensifentrine and muscarinic antagonists, underpinning the rationale for a combination approach. This has led to the conceptualization of \"trifunctional dual bronchodilation,\" describing a regimen that simultaneously targets distinct bronchodilatory mechanisms and provides robust anti-inflammatory effects. Such a strategy may support corticosteroid stewardship by reducing inhaled corticosteroid use, particularly in patients with low eosinophil counts or corticosteroid resistance. However, limitations remain, including the absence of head-to-head trials against existing triple therapy, high cost, and reliance on nebulized delivery. Future research should evaluate long-term outcomes, optimal placement within treatment algorithms, and potential benefits of dry powder or metered-dose formulations. Overall, ensifentrine, especially in combination with a LAMA, may redefine maintenance therapy in COPD, offering a steroid-sparing alternative grounded in mechanistic synergy and clinical efficacy.</p>","PeriodicalId":11482,"journal":{"name":"Drugs","volume":" ","pages":"1099-1107"},"PeriodicalIF":14.4000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12414029/pdf/","citationCount":"0","resultStr":"{\"title\":\"Ensifentrine Plus a Long-Acting Muscarinic Antagonist in COPD: A Trifunctional Dual Bronchodilation Perspective.\",\"authors\":\"Mario Cazzola, Clive P Page, Luigino Calzetta, Fernando J Martinez, Paola Rogliani, Maria Gabriella Matera\",\"doi\":\"10.1007/s40265-025-02213-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Chronic obstructive pulmonary disease (COPD) management has evolved with the emergence of advanced pharmacological strategies, notably dual bronchodilation and bifunctional agents. Among these innovations, the selective inhaled phosphodiesterase (PDE)3/4 inhibitor ensifentrine represents a novel therapeutic class that combines bronchodilatory and anti-inflammatory properties within a single molecular entity. Dual bronchodilation, traditionally achieved through the combination of long-acting muscarinic antagonists (LAMAs) and long-acting β<sub>2</sub>-agonists, has demonstrated superior efficacy compared with monotherapies, including enhanced pulmonary function, reduced symptom burden, and decreased exacerbation frequency. Ensifentrine, recently approved by the US Food and Drug Administration, exerts bronchodilation via PDE3 inhibition and suppresses inflammation by inhibiting PDE4, offering complementary benefits when combined with LAMAs. Clinical trials, including ENHANCE-1 and ENHANCE-2, have shown that ensifentrine significantly improves FEV<sub>1</sub>, reduces exacerbations, and lowers inflammatory biomarkers, with a favorable safety profile. Notably, preclinical and clinical data suggest synergism between ensifentrine and muscarinic antagonists, underpinning the rationale for a combination approach. This has led to the conceptualization of \\\"trifunctional dual bronchodilation,\\\" describing a regimen that simultaneously targets distinct bronchodilatory mechanisms and provides robust anti-inflammatory effects. Such a strategy may support corticosteroid stewardship by reducing inhaled corticosteroid use, particularly in patients with low eosinophil counts or corticosteroid resistance. However, limitations remain, including the absence of head-to-head trials against existing triple therapy, high cost, and reliance on nebulized delivery. Future research should evaluate long-term outcomes, optimal placement within treatment algorithms, and potential benefits of dry powder or metered-dose formulations. Overall, ensifentrine, especially in combination with a LAMA, may redefine maintenance therapy in COPD, offering a steroid-sparing alternative grounded in mechanistic synergy and clinical efficacy.</p>\",\"PeriodicalId\":11482,\"journal\":{\"name\":\"Drugs\",\"volume\":\" \",\"pages\":\"1099-1107\"},\"PeriodicalIF\":14.4000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12414029/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drugs\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s40265-025-02213-w\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/24 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drugs","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s40265-025-02213-w","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/24 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

随着先进药理学策略的出现,慢性阻塞性肺疾病(COPD)的治疗也在不断发展,尤其是双重支气管扩张和双功能药物。在这些创新中,选择性吸入磷酸二酯酶(PDE)3/4抑制剂ensifentrine代表了一种新的治疗类别,它在单个分子实体中结合了支气管扩张和抗炎特性。双重支气管扩张,传统上是通过长效毒蕈碱拮抗剂(LAMAs)和长效β2激动剂的联合治疗来实现的,与单一治疗相比,已经证明了更好的疗效,包括增强肺功能,减轻症状负担,降低恶化频率。Ensifentrine最近被美国食品和药物管理局批准,通过抑制PDE3发挥支气管扩张作用,并通过抑制PDE4抑制炎症,与LAMAs联合使用时提供互补的益处。包括ENHANCE-1和ENHANCE-2在内的临床试验表明,ensifentrine可显著改善FEV1,减少恶化,降低炎症生物标志物,并具有良好的安全性。值得注意的是,临床前和临床数据表明,埃斯芬汀和毒蕈碱拮抗剂之间存在协同作用,这支持了联合用药的基本原理。这导致了“三功能双重支气管扩张”的概念,描述了一种同时针对不同支气管扩张机制并提供强大抗炎作用的方案。这种策略可以通过减少吸入皮质类固醇的使用来支持皮质类固醇的管理,特别是在嗜酸性粒细胞计数低或皮质类固醇抵抗的患者中。然而,局限性仍然存在,包括缺乏对现有三联疗法的正面试验,成本高,依赖雾化输送。未来的研究应评估长期结果、治疗算法中的最佳位置以及干粉或计量制剂的潜在益处。总的来说,恩西芬汀,特别是与LAMA联合使用,可能重新定义COPD的维持治疗,提供一种基于机制协同作用和临床疗效的节省类固醇的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ensifentrine Plus a Long-Acting Muscarinic Antagonist in COPD: A Trifunctional Dual Bronchodilation Perspective.

Ensifentrine Plus a Long-Acting Muscarinic Antagonist in COPD: A Trifunctional Dual Bronchodilation Perspective.

Chronic obstructive pulmonary disease (COPD) management has evolved with the emergence of advanced pharmacological strategies, notably dual bronchodilation and bifunctional agents. Among these innovations, the selective inhaled phosphodiesterase (PDE)3/4 inhibitor ensifentrine represents a novel therapeutic class that combines bronchodilatory and anti-inflammatory properties within a single molecular entity. Dual bronchodilation, traditionally achieved through the combination of long-acting muscarinic antagonists (LAMAs) and long-acting β2-agonists, has demonstrated superior efficacy compared with monotherapies, including enhanced pulmonary function, reduced symptom burden, and decreased exacerbation frequency. Ensifentrine, recently approved by the US Food and Drug Administration, exerts bronchodilation via PDE3 inhibition and suppresses inflammation by inhibiting PDE4, offering complementary benefits when combined with LAMAs. Clinical trials, including ENHANCE-1 and ENHANCE-2, have shown that ensifentrine significantly improves FEV1, reduces exacerbations, and lowers inflammatory biomarkers, with a favorable safety profile. Notably, preclinical and clinical data suggest synergism between ensifentrine and muscarinic antagonists, underpinning the rationale for a combination approach. This has led to the conceptualization of "trifunctional dual bronchodilation," describing a regimen that simultaneously targets distinct bronchodilatory mechanisms and provides robust anti-inflammatory effects. Such a strategy may support corticosteroid stewardship by reducing inhaled corticosteroid use, particularly in patients with low eosinophil counts or corticosteroid resistance. However, limitations remain, including the absence of head-to-head trials against existing triple therapy, high cost, and reliance on nebulized delivery. Future research should evaluate long-term outcomes, optimal placement within treatment algorithms, and potential benefits of dry powder or metered-dose formulations. Overall, ensifentrine, especially in combination with a LAMA, may redefine maintenance therapy in COPD, offering a steroid-sparing alternative grounded in mechanistic synergy and clinical efficacy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Drugs
Drugs 医学-毒理学
CiteScore
22.70
自引率
0.90%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Drugs is a journal that aims to enhance pharmacotherapy by publishing review and original research articles on key aspects of clinical pharmacology and therapeutics. The journal includes: Leading/current opinion articles providing an overview of contentious or emerging issues. Definitive reviews of drugs and drug classes, and their place in disease management. Therapy in Practice articles including recommendations for specific clinical situations. High-quality, well designed, original clinical research. Adis Drug Evaluations reviewing the properties and place in therapy of both newer and established drugs. AdisInsight Reports summarising development at first global approval. Moreover, the journal offers additional digital features such as animated abstracts, video abstracts, instructional videos, and podcasts to increase visibility and educational value. Plain language summaries accompany articles to assist readers with some knowledge of the field in understanding important medical advances.
×
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