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Tacrolimus Ointment in the Treatment of Chronic Cutaneous Graft-vs-Host Disease
A Case Series of 18 Patients
Caroline J. Choi, MD;
Paul Nghiem, MD, PhD
Arch Dermatol. 2001;137:1202-1206.
Background Tacrolimus (formerly FK 506) is an immunosuppressive drug that works by inhibiting calcineurin, a calcium-dependent protein phosphatase required for immune function. Tacrolimus has been shown to be effective topically in atopic dermatitis and systemically in psoriasis and graft-vs-host disease (GVHD). However, its efficacy in treating cutaneous GVHD when applied topically has not been reported.
Objective To assess the therapeutic efficacy of 0.1% tacrolimus ointment on chronic cutaneous GVHD in patients with symptoms refractory to systemic corticosteroid therapy.
Results Tacrolimus ointment effectively treated pruritus and/or erythema in 13 (72%) of 18 patients with chronic GVHD. Responding patients had a rapid effect within several hours to days. Effectiveness was measured by means of patient report, results of physical examination, side-by-side comparisons of tacrolimus vs a vehicle control, and temporal flares of the cutaneous symptoms of the disease in the context of stopping tacrolimus ointment therapy. Because of the progression of GVHD and in 2 cases, loss of drug efficacy, all patients eventually went on to receive more aggressive treatment, including increases in steroid dosage, psoralenUV-A therapy, and extracorporeal photopheresis.
Conclusions This case series suggests that tacrolimus ointment has efficacy in treating the erythema and pruritus of steroid-refractory, chronic cutaneous GVHD in most patients. The rapid response of tacrolimus ointment may provide a useful therapeutic bridge to systemic therapies that have slower onset, such as psoralenUV-A therapy or extracorporeal photopheresis.
From the Department of Dermatology, Brigham and Women's Hospital and Dana Farber Cancer Institute, Harvard Medical School, Boston, Mass (Drs Choi and Nghiem); and the Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Mass (Dr Nghiem). The authors have no commercial, proprietary, or financial interest in the products or companies described in this article.
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