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A multicentre, randomized, double-blind, controlled study of long-term treatment with 0.1% tacrolimus ointment in adults with moderate to severe atopic dermatitis
被引:96
|作者:
Reitamo, S
Ortonne, JP
Sand, C
Cambazard, F
Bieber, T
Fölster-Holst, R
Vena, G
Bos, JD
Fabbri, P
Larsen, CG
机构:
[1] Helsinki CHU, Dept Dermatol, SF-00250 Helsinki, Finland
[2] Hop Archet 2, Serv Dermatol, Nice, France
[3] Bispebjerg Hosp, Dept Dermatol, DK-2400 Copenhagen, Denmark
[4] Hop Nord St Etienne, Serv Dermatol, St Etienne, France
[5] Univ Bonn, Dermatol Klin & Poliklin, D-5300 Bonn, Germany
[6] Univ Kiel, Dermatol Klin, Kiel, Germany
[7] Policlin Consorziale Bari, Unita Operat Dermatol 2, Bari, Italy
[8] Univ Amsterdam, Acad Med Ctr, Dept Dermatol, NL-1105 AZ Amsterdam, Netherlands
[9] Univ Florence, Clin Dermosifilopat 2, Florence, Italy
[10] Marselisborg Hosp, Dept Dermatol, DK-8000 Aarhus, Denmark
关键词:
atopic dermatitis;
efficacy;
long-term treatment;
randomized controlled trial;
safety 0-1% tacrolimus;
D O I:
10.1111/j.1365-2133.2005.06592.x
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Background Atopic dermatis (AD) is a chronic disease that often requires long-term treatment. Topical corticosteroids are the usual therapy for patients with AD, but prolonged usage can result in skin atrophy and other side-effects. Objectives In a randomized, double-blind, comparative study, to compare the efficacy and safety of a 6-month treatment period with 0.1% tacrolimus ointment vs. a corticosteroid ointment regimen in adults with moderate to severe AD. Methods Treatment was applied twice daily for a maximum of 6 months. Patients in the tacrolimus treatment group (n = 487) applied 0.1% tacrolimus ointment to all affected areas over the whole body. The patients treated with the corticosteroid regimen (n = 485) applied 0.1% hydrocortisone butyrate ointment to affected areas on the trunk and extremities and 1% hydrocortisone acetate ointment to affected areas on the face and neck. The study primary endpoint was the response rate, i.e. the proportion of patients with at least 60% improvement in the modified Eczema Area and Severity Index (mEASI) between baseline and month 3. Results By month 3, more patients in the 0.1% tacrolimus group responded to treatment (72.6% vs. 52.3% in the corticosteroid group, P < 0.001). The patients treated with 0.1% tacrolimus also showed greater improvement in mEASI, EASI, affected body surface area and physician and patient assessments of global response. Patients applying 0.1% tacrolimus ointment experienced more skin burning (52.4% vs. 13.8% in the corticosteroid group; P < 0.001). In most patients, skin burning was mild to moderate in severity and decreased rapidly after the first week of treatment. There was no increase in the incidence of infections or malignancies over time in either treatment group. Conclusions Long-term treatment with 0.1% tacrolimus ointment is significantly more efficacious than a corticosteroid ointment regimen in adults with moderate to severe AD.
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页码:1282 / 1289
页数:8
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