LABA/LAMA fixed-dose combinations in patients with COPD: a systematic review

被引:33
作者
Rogliani, Paola [1 ]
Calzetta, Luigino [1 ]
Braido, Fulvio [2 ]
Cazzola, Mario [1 ]
Clini, Enrico [3 ]
Pelaia, Girolamo [4 ]
Rossi, Andrea [5 ]
Scichilone, Nicola [6 ]
Di Marco, Fabiano [7 ]
机构
[1] Univ Roma Tor Vergata, Dept Expt Med & Surg, Via Montpellier 1, I-00133 Rome, Italy
[2] IRCCS San Martino Genoa Univ Hosp, Dept Internal Med, Genoa, Italy
[3] Univ Modena & Reggio Emilia, Dept Med & Surg Sci, Modena, Italy
[4] Magna Graecia Univ Catanzaro, Sect Resp Dis, Dept Med & Surg Sci, Catanzaro, Italy
[5] Univ Verona, Pulm Unit, Verona, Italy
[6] Univ Palermo, Dept Internal Med, Palermo, Italy
[7] Univ Milan, Papa Giovanni Hosp 23, Dept Hlth Sci, Resp Unit, Bergamo, Italy
关键词
LABA; LAMA; fixed-dose combination; COPD; systematic review; ACLIDINIUM BROMIDE/FORMOTEROL FUMARATE; INHALED BETA(2)-ADRENOCEPTOR AGONIST; UMECLIDINIUM/VILANTEROL; 62.5/25; MCG; ACTING MUSCARINIC ANTAGONISTS; LONG-TERM SAFETY; TO-SEVERE COPD; DOUBLE-BLIND; PHARMACOLOGICAL CHARACTERIZATION; IN-VITRO; FLUTICASONE PROPIONATE/SALMETEROL;
D O I
10.2147/COPD.S170606
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Objectives: The aim of this study was to assess the current evidence for long-acting beta(2)-agonist (LABA)/long-acting muscarinic antagonist (LAMA) fixed-dose combinations (FDCs) in the treatment of COPD. Materials and methods: A systematic literature search of randomized controlled trials published in English up to September 2017 of LABA/LAMA FDCs vs LABA or LAMA or LABA/inhaled corticosteroid (ICS) FDCs in COPD patients was performed using PubMed, Embase, Scopus, and Google Scholar. Outcomes including forced expiratory volume in 1 second (FEV1), Transition Dyspnea Index (TDI) scores, St George's Respiratory Questionnaire (SGRQ) scores, exacerbations, exercise tolerance (endurance time [ET]), inspiratory capacity (IC), and rescue medication use were evaluated. Results: In total, 27 studies were included in the review. LABA/LAMA FDCs significantly improved lung function (FEV1) at 12 weeks compared with LABA or LAMA or LABA/ICS. These effects were maintained over time. Significant improvements with LABA/LAMA FDCs vs each evaluated comparator were also observed in TDI and SGRQ scores, even if significant differences between different LABA/LAMA FDCs were detected. Only the LABA/LAMA FDC indacaterol/glycopyrronium has shown superiority vs LAMA and LABA/ICS for reducing exacerbation rates, while olodaterol/tiotropium and indacaterol/glycopyrronium have been shown to improve ET and IC vs the active comparators. Rescue medication use was significantly reduced by LABA/LAMA FDCs vs the evaluated comparators. LABA/LAMA FDCs were safe, with no increase in the risk of adverse events with LABA/LAMA FDCs vs the monocomponents. Conclusion: Evidence supporting the efficacy of LABA/LAMA FDCs for COPD is heterogeneous, particularly for TDI and SGRQ scores, exacerbation rates, ET, and IC. So far, indacaterol/glycopyrronium is the LABA/LAMA FDC that has the strongest evidence for superiority vs LABA, LAMA, and LABA/ICS FDCs across the evaluated outcomes. LABA/LAMA FDCs were safe; however, more data should be collected in a real-world setting to confirm their safety.
引用
收藏
页码:3115 / 3130
页数:16
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