Global Initiative for Asthma 2016-derived asthma control with fluticasone propionate and salmeterol A Gaining Optimal Asthma Control (GOAL) study reanalysis

被引:14
作者
Bateman, Eric D. [1 ]
Busse, William [2 ]
Pedersen, Soren E. [3 ]
Bousquet, Jean [4 ]
Huang, Shaoguang [5 ]
Zhou, Xin [6 ]
Gul, Nadeem [7 ]
Hollis, Sally [8 ]
Gibbs, Michael [7 ]
机构
[1] Univ Cape Town, Div Pulmonol, Dept Med, Cape Town, South Africa
[2] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI USA
[3] Univ Southern Denmark, Kolding Hosp, Pediat Res Unit, Kolding, Denmark
[4] Univ Montpellier, European Innovat Partnership Active & Healthy Age, Fdn MACVIA LR, Malad Chron Vieillissement Actif Languedoc Roussi, Montpellier, France
[5] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Resp Med, Shanghai, Peoples R China
[6] Shanghai First Peoples Hosp, Shanghai, Peoples R China
[7] Global Resp Franchise, GSK House, Brentford, Middlesex, England
[8] Phastar, London, England
关键词
SEVERITY; QUALITY; DEVICE;
D O I
10.1016/j.anai.2019.04.018
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: In 2004, the landmark Gaining Optimal Asthma Control (GOAL) study demonstrated that most patients can achieve asthma control through sustained treatment and that adding a long-acting beta(2)-adrenoreceptor agonist to an inhaled corticosteroid (ICS) is more effective than ICS alone in this regard. Definitions of asthma control have since evolved, and the consequent implications for the GOAL study findings are unclear. Objective: To evaluate the efficacy of fluticasone propionate and salmeterol and fluticasone propionate alone in achieving and maintaining asthma control, as derived from the Global Initiative for Asthma (GINA) 2016 report. Methods: In total, 3416 patients were stratified by prior medication (ICS-naive [stratum 1], low-dose ICS [stratum 2], or medium-dose ICS [stratum 3]) and randomized to receive fluticasone propionate and salmeterol or fluticasone propionate. The primary end point was the proportion of patients achieving well-controlled or partly controlled asthma; secondary end points included the proportion of patients achieving well-controlled asthma. Control was evaluated during the last 4 weeks of each dose titration. Results: In all strata, more patients achieved well-controlled or partly controlled asthma with fluticasone propionate and salmeterol vs fluticasone propionate alone (stratum 1: 91% vs 85%; P = .003; stratum 2: 86% vs 82%; P = .07; and stratum 3: 76% vs 66%; P < .001), as well as patients with well-controlled asthma (stratum 1: 64% vs 56%; P = .005; stratum 2: 59% vs 41%; P < .001; and stratum 3: 40% vs 22%; P < .001). Conclusion: A markedly higher proportion of patients with uncontrolled asthma in each stratum achieved control according to GINA 2016 criteria compared with the original study criteria. The proportion of patients achieving control remained greater with fluticasone propionate and salmeterol than with fluticasone propionate alone. (C) 2019 Published by Elsevier Inc. on behalf of American College of Allergy, Asthma & Immunology.
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收藏
页码:57 / +
页数:9
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