Comparison of fluticasone propionate-salmeterol combination therapy and montelukast in patients who are symptomatic on short-acting beta(2)-agonists alone

The objective of this study was to determine whether initial maintenance th erapy for the treatment of inflammation and bronchoconstriction associated with persistent asthma is more effective with a combination product (100 mu g of fluticasone propionate and 50 mug of salmeterol [FSC]) administered tw ice daily through the Diskus device (GlaxoWellcome, Research Triangle Park, NQ or with montelukast at 10 mg once daily. A 12-wk, randomized, double-bl ind, double-dummy, multicenter study was conducted with 423 patients 15 yr of age and older with asthma and who were symptomatic while receiving short -acting beta (2)-agonists alone. At end point, FSC resulted in significantl y greater increases in morning predose FEV, (0.54 +/- 0.03 vs. 0.27 +/- 0.0 3 L), morning peak expiratory flow (PEP) (89.9 +/- 6.7 vs. 34.2 +/- 4.7 L/m in), evening PEP (69.9 +/- 5.8 vs. 31.1 +/- 4.5 L/min), the percentage of s ymptom-free days (48.9 +/- 2.9 vs. 21.7 +/- 2.5%), the percentage of rescue -free days (53.0 +/- 2.8 vs. 26.2 +/- 2.5%), and the percentage of nights w ith no awakenings (23.0 +/- 2.5 vs. 15.5 +/- 2.4%) compared with montelukas t (p less than or equal to 0.001, all comparisons). FSC significantly reduc ed asthma symptom scores (-1.0 +/- 0.1 vs. -0.6 +/- 0.1), rescue albuterol use (-3.3 +/- 0.2 vs. -1.9 +/- 0.2 puffs/d), and the number of exacerbation s (0 vs. 11) compared with montelukast (p < 0.001). Both treatments were we ll tolerated. In summary, treatment of the two main components of asthma (i nflammation and bronchoconstriction) with fluticasone propionate and salmet erol in a combination product was a more effective initial maintenance trea tment strategy than treatment with montelukast, a single-mediator antagonis t.