1. [Analysis of a case series of adult patients with severe atopic dermatitis treated with dupilumab in Argentina].
- Author
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Máspero J, Angles MV, Ardusso L, Brancciforte M, Castro C, Cruz Iturrieta C, Chouela E, De Gennaro MS, Fernández Bussy R, Galimberti ML, Galimberti RL, Gattolin G, Luna PC, Magariños G, Marini MG, Maskin M, Plafnik R, Raimondo N, Russo JP, Sevinsky L, and Stringa MF
- Subjects
- Adolescent, Adult, Aged, Argentina, Female, Follow-Up Studies, Humans, Male, Middle Aged, Retrospective Studies, Severity of Illness Index, Treatment Outcome, Young Adult, Antibodies, Monoclonal, Humanized therapeutic use, Dermatitis, Atopic drug therapy, Dermatologic Agents therapeutic use
- Abstract
Introduction: Severe atopic dermatitis (AD) treatment is an unmet need, given the limited efficacy and safety of classical systemic treatments (CSTs). Dupilumab is a monoclonal antibody that blocks the signaling of the interleukins that mediate the inflammatory response involved in AD., Methods: the clinical response of a group of patients from Argentina with severe AD and insufficient response and/or toxicity to CSTs who were treated with dupilumab before commercial availability was analyzed. EASI, SCORAD, DLQI scales and analog visual scales of pruritus and sleep were evaluated, during a median follow-up of 189 days. In addition, the incidence of adverse events was analyzed., Results: 20 patients (13 male) were included; median age: 37.5 years; median AD evolution: 20 years; atopic comorbidity: 70%. 100% had received systemic corticosteroids (serious complications: 20%). Main reasons for discontinuation of CSTs were lack of efficacy and occurrence of adverse events. All scores were significantly and steadily reduced, with identifiable clinical response at the second month of treatment. At the end of the follow-up, only 3 patients required concomitant systemic immunosuppressive treatment. Dupilumab was well tolerated, with mild and controllable adverse events., Discussion: Dupilumab is the only biological agent with high efficacy demonstrated in clinical and observational studies. In this case series, its effectiveness was confirmed in difficult-to-treat patients with severe AD and inadequate response to CSTs. The safety profile was favorable and consistent., (Universidad Nacional de Córdoba)
- Published
- 2020
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