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Volume 183, Issue 4, Pages 1395-1399 (April 2010)


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Acitretin for Severe Lichen Sclerosus of Male Genitalia: A Randomized, Placebo Controlled Study

D. Ioannides, E. LazaridouCorresponding Author Informationemail address, Z. Apalla, E. Sotiriou, S. Gregoriou, D. Rigopoulos

Received 12 July 2009 published online 19 February 2010.

Purpose

Genital lichen sclerosus is a chronic inflammatory and fibrosclerotic disease associated with substantial morbidity. Acitretin has been reported to be of benefit in many dermatological indications including lichen sclerosus. We evaluated the efficacy and tolerability of acitretin for biopsy confirmed, severe lichen sclerosus of the male genitalia.

Materials and Methods

A randomized, double-blind, placebo controlled study was performed in which 52 male patients with severe, long-standing lichen sclerosus were randomized in a 2:1 ratio to receive daily acitretin (35 mg) or placebo for 20 consecutive weeks. Followup lasted for 36 weeks from baseline. The primary end point was complete response of active lichen sclerosus as well as improvement of patient quality of life. Secondary end points were partial response and recurrence rates after treatment discontinuation.

Results

A total of 49 patients completed the study and were eligible for statistical analysis. Complete response was achieved by 36.4% (12 of 33) of the acitretin group vs 6.3% (1 of 16) of the controls, while 36.4% (12 of 33) vs 12.5% (2 of 16) achieved partial resolution, respectively. Mean total clinical score of the acitretin group was significantly lower than that of the controls at week 20 [t (47) = −4.146, p = 0.00 < 0.5], which was also accompanied by a significant improvement in mean Dermatology Life Quality Index score [t (32) = 6,441, p = 0.000 < 0.05]. Acitretin was well tolerated and only minimal transient side effects were recorded.

Conclusions

Acitretin is safe and effective for the management of severe, long-standing lichen sclerosus of the male genitalia. Study limitations included bias during clinical evaluation considering the expected side effects of acitretin.

First Department of Dermatology-Venereology, Aristotle University Medical School, Thessaloniki, and First Department of Dermatology, A. Sygros Hospital, University of Athens Medical School, Athens (SG, DR), Greece

Corresponding Author InformationCorrespondence: 133 Tsimiski St., 546 21, Thessaloniki, Greece (telephone: +302310 242433; FAX: +302310 271749)

 Study received institutional ethical committee approval.

PII: S0022-5347(09)03234-0

doi:10.1016/j.juro.2009.12.057


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