TY - JOUR
T1 - Tiotropium bromide step-up therapy for adults with uncontrolled asthma
AU - Peters, Stephen P.
AU - Kunselman, Susan J.
AU - Icitovic, Nikolina
AU - Moore, Wendy C.
AU - Pascual, Rodolfo
AU - Ameredes, Bill T.
AU - Boushey, Homer A.
AU - Calhoun, William J.
AU - Castro, Mario
AU - Cherniack, Reuben M.
AU - Craig, Timothy
AU - Denlinger, Loren
AU - Engle, Linda L.
AU - DiMango, Emily A.
AU - Fahy, John V.
AU - Israel, Elliot
AU - Jarjour, Nizar
AU - Kazani, Shamsah D.
AU - Kraft, Monica
AU - Lazarus, Stephen C.
AU - Lemanske, Robert F.
AU - Lugogo, Njira
AU - Martin, Richard J.
AU - Meyers, Deborah A.
AU - Ramsdell, Joe
AU - Sorkness, Christine A.
AU - Sutherland, E. Rand
AU - Szefler, Stanley J.
AU - Wasserman, Stephen I.
AU - Walter, Michael J.
AU - Wechsler, Michael E.
AU - Chinchilli, Vernon M.
AU - Bleecker, Eugene R.
PY - 2010/10/28
Y1 - 2010/10/28
N2 - BACKGROUND: Long-acting beta-agonist (LABA) therapy improves symptoms in patients whose asthma is poorly controlled by an inhaled glucocorticoid alone. Alternative treatments for adults with uncontrolled asthma are needed. METHODS: In a three-way, double-blind, triple-dummy crossover trial involving 210 patients with asthma, we evaluated the addition of tiotropium bromide (a long-acting anticholinergic agent approved for the treatment of chronic obstructive pulmonary disease but not asthma) to an inhaled glucocorticoid, as compared with a doubling of the dose of the inhaled glucocorticoid (primary superiority comparison) or the addition of the LABA salmeterol (secondary noninferiority comparison). RESULTS: The use of tiotropium resulted in a superior primary outcome, as compared with a doubling of the dose of an inhaled glucocorticoid, as assessed by measuring the morning peak expiratory flow (PEF), with a mean difference of 25.8 liters per minute (P<0.001) and superiority in most secondary outcomes, including evening PEF, with a difference of 35.3 liters per minute (P<0.001); the proportion of asthmacontrol days, with a difference of 0.079 (P = 0.01); the forced expiratory volume in 1 second (FEV1) before bronchodilation, with a difference of 0.10 liters (P = 0.004); and daily symptom scores, with a difference of -0.11 points (P<0.001). The addition of tiotropium was also noninferior to the addition of salmeterol for all assessed outcomes and increased the prebronchodilator FEV1 more than did salmeterol, with a difference of 0.11 liters (P = 0.003). CONCLUSIONS: When added to an inhaled glucocorticoid, tiotropium improved symptoms and lung function in patients with inadequately controlled asthma. Its effects appeared to be equivalent to those with the addition of salmeterol. (Funded by the National Heart, Lung, and Blood Institute; ClinicalTrials.gov number, NCT00565266.).
AB - BACKGROUND: Long-acting beta-agonist (LABA) therapy improves symptoms in patients whose asthma is poorly controlled by an inhaled glucocorticoid alone. Alternative treatments for adults with uncontrolled asthma are needed. METHODS: In a three-way, double-blind, triple-dummy crossover trial involving 210 patients with asthma, we evaluated the addition of tiotropium bromide (a long-acting anticholinergic agent approved for the treatment of chronic obstructive pulmonary disease but not asthma) to an inhaled glucocorticoid, as compared with a doubling of the dose of the inhaled glucocorticoid (primary superiority comparison) or the addition of the LABA salmeterol (secondary noninferiority comparison). RESULTS: The use of tiotropium resulted in a superior primary outcome, as compared with a doubling of the dose of an inhaled glucocorticoid, as assessed by measuring the morning peak expiratory flow (PEF), with a mean difference of 25.8 liters per minute (P<0.001) and superiority in most secondary outcomes, including evening PEF, with a difference of 35.3 liters per minute (P<0.001); the proportion of asthmacontrol days, with a difference of 0.079 (P = 0.01); the forced expiratory volume in 1 second (FEV1) before bronchodilation, with a difference of 0.10 liters (P = 0.004); and daily symptom scores, with a difference of -0.11 points (P<0.001). The addition of tiotropium was also noninferior to the addition of salmeterol for all assessed outcomes and increased the prebronchodilator FEV1 more than did salmeterol, with a difference of 0.11 liters (P = 0.003). CONCLUSIONS: When added to an inhaled glucocorticoid, tiotropium improved symptoms and lung function in patients with inadequately controlled asthma. Its effects appeared to be equivalent to those with the addition of salmeterol. (Funded by the National Heart, Lung, and Blood Institute; ClinicalTrials.gov number, NCT00565266.).
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U2 - 10.1056/NEJMoa1008770
DO - 10.1056/NEJMoa1008770
M3 - Article
C2 - 20979471
AN - SCOPUS:77957768543
SN - 0028-4793
VL - 363
SP - 1715
EP - 1726
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 18
ER -