Superiority of tacrolimus 0•1% ointment compared with fluticasone 0•005% in adults with moderate to severe atopic dermatitis of the face: results from a randomized, double-blind trial

被引:35
作者
Doss, N. [1 ]
Reitamo, S. [2 ]
Dubertret, L. [3 ]
Fekete, G. L. [4 ]
Kamoun, M. -R. [5 ]
Lahfa, M. [3 ]
Ortonne, J. -P. [6 ]
机构
[1] Mil Hosp Tunis, Dept Dermatol, Tunis 1006, Tunisia
[2] Univ Helsinki, Cent Hosp, Dept Dermatol, FIN-00170 Helsinki, Finland
[3] Hop St Louis, Dept Dermatol, Paris, France
[4] Emergency Hosp Targu Mures, Dermatol Clin, Targu Mures, Romania
[5] Hop Charles Nicolle, Dept Dermatol, Tunis, Tunisia
[6] Hop Archet, Dept Dermatol, Nice, France
关键词
atopic dermatitis; chronic facial erythema; clinical trial; fluticasone propionate ointment; tacrolimus ointment; topical calcineurin inhibitors; TOPICAL CORTICOSTEROIDS; CALCINEURIN INHIBITORS; EFFICACY; SAFETY; PRURITUS; EXPOSURE;
D O I
10.1111/j.1365-2133.2009.09143.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background No specific data are available on tacrolimus ointment as a second-line treatment in adults with facial eczema. Objectives To compare tacrolimus 0 center dot 1% and fluticasone 0 center dot 005% ointments in adults with moderate to severe atopic dermatitis (AD) of the face in whom conventional treatment was ineffective or poorly tolerated. Methods Patients were randomized to double-blind treatment of facial AD with twice-daily tacrolimus ointment (n = 288) or fluticasone ointment (n = 280) for 3 weeks or until clearance. After day 21, patients could continue without the study treatment, apply the same ointment once daily, or switch to the other medication twice daily, depending on lesion clearance and patient/physician satisfaction. The primary endpoint was the day-21 response [>= 60% reduction in the modified Local Eczema and Severity Index (mLEASI) score]. Secondary endpoints included facial erythema and pruritus, global clinical response, treatment switching at day 21 and safety. Results Response with tacrolimus ointment (93%) was superior to that with fluticasone (88%; P = 0 center dot 026). Improvements in mLEASI components were also greater with tacrolimus ointment. Facial erythema and pruritus improved in both groups. Global clinical response was rated 'marked improvement' or better in 88% and 79% of patients in the tacrolimus ointment and fluticasone groups, respectively. At day 21, 9% of patients switched from fluticasone to tacrolimus ointment, while 4 center dot 5% switched from tacrolimus ointment to fluticasone. Adverse events were more frequent with tacrolimus ointment as a result of the higher incidence of application-site skin burning sensation. Safety of both drugs was in line with their respective summary of product characteristics. Conclusions Tacrolimus 0 center dot 1% ointment has superior efficacy to fluticasone 0 center dot 005% ointment for twice-daily treatment of adults with moderate to severe facial AD in whom conventional therapy was inadequately effective or not tolerated. Tacrolimus 0 center dot 1% ointment is a safe and effective second-line treatment for the control of moderate to severe AD of the face.
引用
收藏
页码:427 / 434
页数:8
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