用于治疗慢性阻塞性肺疾病的新型吸入式 PDE3 和 PDE4 双抑制剂安西芬净:根据 PRISMA 声明对低谷 FEV1 和病情恶化进行的系统综述和荟萃分析方案

Q2 Agricultural and Biological Sciences Current Research in Pharmacology and Drug Discovery Pub Date : 2024-01-01 DOI:10.1016/j.crphar.2024.100195
Luigino Calzetta , Mario Cazzola , Shima Gholamalishahi , Paola Rogliani
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引用次数: 0

摘要

吸入性磷酸二酯酶(PDE)3 和 PDE4 双抑制剂安非他酮用于慢性阻塞性肺病(COPD)维持治疗的研究引起了极大的临床兴趣。尽管最近的 III 期试验取得了令人鼓舞的结果,但仍缺乏对其在慢性阻塞性肺病中疗效的全面综述。本方案概述了 PROSPERO 中首次登记的系统综述和荟萃分析,以评估安非他酮对第一秒用力呼气容积(FEV1)谷值和慢性阻塞性肺疾病急性加重的影响。通过进行严格的文献检索和采用可靠的方法,这项工作旨在为安昔喷丁的实际疗效提供有力的证据。预期结果包括:与对照组相比,接受安非他酮治疗的患者的 FEV1 谷值明显改善,AECOPD 风险降低,证实了其支气管扩张和抗炎特性。荟萃分析有望揭示不同试验的一致结果,从而增强对研究结果的信心。此外,亚组分析可能会揭示影响安塞芬净疗效的因素,从而指导最佳治疗策略。总之,该方案有望为临床实践和监管决策提供依据,并将安非他酮定位为慢性阻塞性肺疾病治疗的重要补充药物。
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The novel inhaled dual PDE3 and PDE4 inhibitor ensifentrine for the treatment of COPD: A systematic review and meta-analysis protocol on trough FEV1 and exacerbation according to PRISMA statement

The investigation of ensifentrine, an inhaled dual phosphodiesterase (PDE)3 and PDE4 inhibitor, for chronic obstructive pulmonary disease (COPD) maintenance therapy presents a significant clinical interest. Despite promising results from recent Phase III trials, a comprehensive synthesis of its therapeutic efficacy in COPD is lacking. This protocol outlines the first registered systematic review and meta-analysis in PROSPERO to assess the impact of ensifentrine on trough forced expiratory volume in the 1st second (FEV1) and acute exacerbations of COPD. By conducting a rigorous literature search and employing solid methodologies, this endeavour aims to provide robust evidence on the real efficacy of ensifentrine. Anticipated outcomes include a significant improvement in trough FEV1 and a reduction in AECOPD risk among ensifentrine-treated patients compared to controls, corroborating its bronchodilator and anti-inflammatory properties. The meta-analysis expects to reveal consistent results across different trials, enhancing confidence in the findings. Additionally, subgroup analyses may unveil factors influencing the efficacy of ensifentrine, guiding optimal therapeutic strategies. Overall, this protocol holds the potential to inform clinical practice and regulatory decisions, positioning ensifentrine as a valuable addition to COPD management.

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来源期刊
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
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