Topical clobetasol propionate treatment and cutaneous adverse effects in patients with early-stage mycosis fungoides: an observational study.


Journal

Cutis
ISSN: 2326-6929
Titre abrégé: Cutis
Pays: United States
ID NLM: 0006440

Informations de publication

Date de publication:
May 2020
Historique:
entrez: 1 7 2020
pubmed: 1 7 2020
medline: 23 4 2021
Statut: ppublish

Résumé

Topical superpotent class I corticosteroids (CSs) are highly effective in the treatment of early-stage mycosis fungoides (MF) and are readily available, easily applied, and have minor side effects compared to other topical therapeutic options. Because MF is a chronic disease, prolonged treatment is needed, raising the concern of CS-induced cutaneous adverse effects (AEs). In this observational study, we aimed to evaluate the risk for skin AEs of clobetasol propionate cream 0.05% in patients with early-stage MF. Thirteen consecutive patients with MF were treated with clobetasol propionate cream 0.05% once or twice daily as monotherapy and were followed for 4 to 17 months. One participant was lost to follow-up, and the remaining 12 participants responded to treatment with topical clobetasol propionate with minimal side effects. With proper education and monitoring, topical CSs are a safe and effective mainstay of treatment for patches and flat plaques in patients with early-stage localized MF.

Identifiants

pubmed: 32603400

Substances chimiques

Glucocorticoids 0
Clobetasol ADN79D536H

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

E27-E32

Auteurs

Shamir Geller (S)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA; and Division of Dermatology, Tel Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Israel.

Patricia L Myskowski (PL)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; and Weill Cornell Medicine, USA.

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Classifications MeSH