Singh Dave, Higham Andrew, Mathioudakis Alexander G, Beech Augusta
Division of Immunology, Immunity to Infection and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester and Manchester University NHS Foundation Trust, Manchester, UK.
Medicines Evaluation Unit, The Langley Building, Southmoor Road, Manchester, M23 9QZ, UK.
Drugs. 2025 May 20. doi: 10.1007/s40265-025-02188-8.
The immediate goals of pharmacological management in chronic obstructive pulmonary disease (COPD) are to minimise symptoms and improve exercise performance. The longer-term goals are to reduce the future risk of exacerbations, lung function decline and mortality. It is now recognised that a subset of COPD patients have type 2 inflammation, which is identified by the presence of higher blood eosinophil counts (BEC). Individuals with higher BEC show a greater response to pharmacological interventions targeting type 2 inflammation, including inhaled corticosteroids and the monoclonal antibody, dupilumab. The use of BEC as a biomarker to guide pharmacological treatment has enabled a precision medicine approach in COPD. This article reviews recent advances in the pharmacological treatment of COPD, encompassing the optimum use of inhaled combination treatments and the evidence to support the use of the novel inhaled phosphodiesterase inhibitor ensifentrine and monoclonal antibodies in patients with COPD.
慢性阻塞性肺疾病(COPD)药物治疗的近期目标是将症状降至最低并改善运动表现。长期目标是降低未来急性加重、肺功能下降和死亡的风险。现在人们认识到,一部分COPD患者存在2型炎症,这可通过较高的血液嗜酸性粒细胞计数(BEC)来确定。BEC较高的个体对针对2型炎症的药物干预(包括吸入性糖皮质激素和单克隆抗体度普利尤单抗)反应更大。使用BEC作为生物标志物来指导药物治疗,已在COPD中实现了精准医学方法。本文综述了COPD药物治疗的最新进展,包括吸入联合治疗的最佳使用,以及支持在COPD患者中使用新型吸入性磷酸二酯酶抑制剂恩昔芬净和单克隆抗体的证据。
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