Dimethyl Fumarate as Therapeutic Alternative in Moderate-to-Severe Psoriasis: Our Experience

Pau Rosés Gibert1, Francisco Javier de la Torre Gomar1, Amaia Saenz Aguirre1

  • 1Dermatology Department, Araba University Hospital, Vitoria-Gasteiz, Spain.

Abstract

Insights

Dimethyl fumarate (DMF) effectively treats moderate-to-severe psoriasis in adults. This study shows significant PASI and BSA score reductions with manageable side effects, indicating DMF

Area of Science:

  • Dermatology
  • Pharmacology

Background:

  • Dimethyl fumarate (DMF) is an approved oral therapy for moderate-to-severe psoriasis requiring systemic treatment.
  • Psoriasis is a chronic autoimmune disease affecting skin, characterized by red, itchy, scaly patches.

Purpose of the Study:

  • To evaluate the clinical experience and treatment outcomes of dimethyl fumarate (DMF) in adult patients with moderate-to-severe psoriasis in Spain.
  • Assess the efficacy and safety profile of DMF for psoriasis management.

Main Methods:

  • Retrospective study of 30 adult patients with moderate-to-severe psoriasis treated with DMF.
  • Treatment duration ranged from 4 to 55 weeks, with a median of 15 weeks.
  • Evaluated Psoriasis Area and Severity Index (PASI) and Body Surface Area (BSA) scores, and documented adverse events (AEs).

Main Results:

  • Significant reductions in PASI and BSA scores observed by week 24.
  • At week 36, 5 patients achieved PASI and BSA scores of 0.
  • Most frequent adverse events included diarrhea (40.0%), flushing (13.3%), and lymphopenia (3.3%); 47.1% of AEs were managed by dose adjustment. Treatment discontinuation due to AEs occurred in 43.3% of patients.

Conclusions:

  • Dimethyl fumarate (DMF) demonstrates efficacy in reducing psoriasis severity.
  • DMF is a potentially safe and effective treatment option for adult patients with moderate-to-severe psoriasis.
  • Adverse event management through dose adjustment is feasible, though discontinuation rates due to AEs should be considered.

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