1. Treatment of erythrodermic psoriasis with biologics: A systematic review
- Author
-
Gabriel Arias-Berrios, Gabriela Pabón-Cartagena, Karina J. Cancel-Artau, Marely Santiago-Vázquez, Rafael F. Martín-García, Leyre A. Falto-Aizpurua, and Osward Y. Carrasquillo
- Subjects
medicine.medical_specialty ,Dermatology ,Antibodies, Monoclonal, Humanized ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,Psoriasis Area and Severity Index ,Internal medicine ,Psoriasis ,Ustekinumab ,medicine ,Adalimumab ,Humans ,Biological Products ,business.industry ,medicine.disease ,Infliximab ,Ixekizumab ,Guselkumab ,030220 oncology & carcinogenesis ,Secukinumab ,business ,Dermatitis, Exfoliative ,medicine.drug - Abstract
Background Biologic medications for plaque psoriasis have been used to treat erythrodermic psoriasis (EP). Since the guidelines for management of EP were published, new biologic medications have been approved for the treatment of plaque psoriasis. Objective To analyze the evidence of biologic medications in the treatment of EP based on response and tolerability. Methods A comprehensive search was conducted with the PubMed, Cochrane Library, Embase, and Scopus databases through December 31, 2018. Studies reporting 1 or more cases of EP, defined as >75% body surface area involvement, in patients aged ≥18 years treated with biologics were included. Baseline Psoriasis Area and Severity Index score, score improvement, and adverse events were documented. Adequate response to treatment was defined as Psoriasis Area and Severity Index ≥50. Results Included were 43 articles, yielding a total of 179 patients. Most patients responded at some point during treatment, with a higher level of evidence for infliximab, ustekinumab, ixekizumab, and guselkumab. Infection was the most common adverse event (n = 35). Limitations Data are limited to case reports, case series, and uncontrolled studies. Conclusion Patients with EP treated with biologics demonstrated positive responses and treatment was well-tolerated, with a weak recommendation and limited quality of evidence in favor of infliximab, ustekinumab, ixekizumab, and guselkumab.
- Published
- 2020
- Full Text
- View/download PDF