2023
DOI: 10.1111/ajd.14081
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Benralizumab: A novel treatment for the cutaneous features of paediatric eosinophilic granulomatosis with polyangiitis (pEGPA)

Abstract: Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis presenting primarily with pulmonary and cutaneous features. The disease is typically seen in the fifth or sixth decade of life (1, 2). We report a case of EGPA in an adolescent who was successfully treated with the interleukin‐5 (IL‐5) receptor inhibitor, benralizumab.

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“…Only one case report describing the efficacy of benralizumab in a 16-year-old boy with antineutrophilic cytoplasmatic antibody-negative EGPA presenting with skin manifestations (eosinophilic infiltration and small-vessel and medium-vessel vasculitis) has been described [ 115 ]. With this exception, there are no studies available for reslizumab and benralizumab in patients aged ≤18 years and the MANDARA trial (NCT04157348), currently comparing mepolizumab versus benralizumab in EGPA excludes patients aged ≤18 years.…”
Section: Eosinophilic Granulomatosis With Polyangiitismentioning
confidence: 99%
“…Only one case report describing the efficacy of benralizumab in a 16-year-old boy with antineutrophilic cytoplasmatic antibody-negative EGPA presenting with skin manifestations (eosinophilic infiltration and small-vessel and medium-vessel vasculitis) has been described [ 115 ]. With this exception, there are no studies available for reslizumab and benralizumab in patients aged ≤18 years and the MANDARA trial (NCT04157348), currently comparing mepolizumab versus benralizumab in EGPA excludes patients aged ≤18 years.…”
Section: Eosinophilic Granulomatosis With Polyangiitismentioning
confidence: 99%