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Tacrolimus ointment 0.1% in the treatment of nickel-induced allergic contact dermatitis - 29/08/11

Doi : 10.1067/S0190-9622(03)01826-7 
Yamini V Saripalli, MD a, Joseph E Gadzia, MD a, Donald V Belsito, MD a,
a Division of Dermatology, University of Kansas Medical Center, Kansas City, Kansas, USA 

*Reprint requests: Donald V. Belsito, MD, Division of Dermatology, University of Kansas Medical Center, 3901 Rainbow Blvd, Kansas City, KS, USA 66160-7319.

Abstract

Background

Tacrolimus is a macrolactam that prevents the transcription of messenger RNA for various inflammatory cytokines in both helper T cells (types 1 and 2) (TH1 and TH2). It is currently approved for the treatment of moderate to severe atopic dermatitis, a Th2-mediated disease, in children and adults.

Objective

We sought to evaluate the safety and efficacy of tacrolimus ointment 0.1% in the treatment of nickel-induced allergic contact dermatitis, a TH1-mediated disease.

Methods

This was a double-blind, randomized, vehicle-controlled, bilateral paired comparison study to assess the safety and efficacy of topical tacrolimus (Protopic, Fujisawa Healthcare Inc, Deerfield, Ill) ointment 0.1% in the treatment of allergic contact dermatitis induced by nickel sulfate. Volunteers were individuals with known hypersensitivity to nickel. Reactivity to nickel was graded both as the investigator's global assessment and total signs and symptoms, which consisted of the cumulative grade from 0 to 4 for each of the following parameters: erythema, induration, vesiculation, and pruritus (range of scores: 0-16). Reactivity was assessed in the per-protocol group at 1 and 2 weeks after beginning treatment with study drug and control. Adverse events were assessed in the intent-to-treat population.

Results

Of the 19 volunteers who completed the study (per protocol), 18 had an improvement in total signs and symptoms with tacrolimus versus 10 patients with the vehicle. Of patients, 80% had an improvement in the investigator's global assessment score on the tacrolimus-treated site versus 30% of patients on the placebo-treated site. Overall, tacrolimus was more effective than placebo in ameliorating the nickel reaction. Although the tacrolimus treated site was clear or almost clear in a greater number of individuals at week 1, this difference did not become significant until the second week of the study. Other than application site burning in 25% of volunteers, no significant adverse events were noted in the intent-to-treat population.

Conclusion

Topical tacrolimus (Protopic, Fujisawa Healthcare Inc) ointment 0.1% may be an option for the treatment of allergic contact dermatitis induced by nickel.

Le texte complet de cet article est disponible en PDF.

Plan


 Supported by Fujisawa Healthcare Inc, Deerfield, Ill.
Disclosure: Both the vehicle and the tacrolimus ointment 0.1% used in this study were manufactured by Fujisawa Healthcare Inc, which funded the study.
An abstract of this study was presented orally at the Experimental Contact Dermatitis Research Group/American Contact Dermatitis Society Combined Biennial Meeting in Cleveland, Ohio, September 20-22, 2002.


© 2003  American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 49 - N° 3

P. 477-482 - septembre 2003 Retour au numéro
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