RT Journal Article
SR Electronic
T1 Clinical efficacy of once-daily mometasone furoate in children with persistent asthma switched from treatment with fluticasone propionate
JF European Respiratory Journal
JO Eur Respir J
FD European Respiratory Society
SP p4006
VO 38
IS Suppl 55
A1 Steven F. Weinstein
A1 Michael Noonan
A1 William E. Berger
A1 Heribert Staudinger
YR 2011
UL http://erj.ersjournals.com/content/38/Suppl_55/p4006.abstract
AB Background: Mometasone furoate (MF) delivered via dry powder inhaler is an inhaled corticosteroid (ICS) for the treatment of persistent asthma in children ≥4 years. MF 110 μg once daily in the evening (QD PM; approved pediatric dose) and MF 110 μg twice daily (BID) were compared with placebo (PBO) in children aged 4–11 years with persistent asthma previously treated with other ICSs at stable doses for ≥2 weeks before randomization. The primary efficacy variable was change from baseline in% predicted forced expiratory volume in 1 s (FEV1) at endpoint; primary results for 296 randomized children were published previously.Objective: Investigate the possible relationship between the primary endpoint and previous ICS use.Methods: Two post hoc analyses were conducted: one to determine whether children previously using different ICSs responded differently to MF; another to compare the effects of MF vs PBO in the subgroup of children previously using fluticasone propionate (FP).Results: In post hoc analysis, no significant difference was found in the response to MF in 296 children previously using different ICSs (P=0.6372). Most children (160; 54%) previously used FP 88–440 μg/d (median, 176 μg/d). Post hoc analysis of treatment effects in the FP subgroup determined that changes in% predicted FEV1 with MF 110 μg QD PM, MF 110 μg BID, and PBO were 6.4%, 4.3%, and -4.2%, respectively. The difference between both doses of MF and PBO was significant (P<0.004).Conclusions: Previous ICS use did not affect the efficacy of MF in children, and MF 110 μg QD PM significantly improved lung function compared with PBO in children switched from FP.