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Pyoderma Gangrenosum and Interleukin Inhibitors: A Semi-Systematic Review
Hakim Ben Abdallah1, Karsten Fogh1, Christian Vestergaard1
1Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
Interleukin inhibitors show promising effectiveness and safety for treating pyoderma gangrenosum (PG) in adults, with high response rates and few adverse events. Further research is needed to confirm these findings and compare specific inhibitors for recalcitrant PG.
Area of Science:
- Dermatology
- Immunology
- Pharmacology
Background:
- Pyoderma gangrenosum (PG) is a rare, severe ulcerative skin disease with significant comorbidities and mortality.
- Current treatment options for PG are limited, with a growing interest in biologics like interleukin inhibitors.
- Existing literature on interleukin inhibitors for PG is sparse, primarily consisting of case reports and series.
Purpose of the Study:
- To systematically review and evaluate the efficacy and safety of interleukin inhibitors in treating adult patients with pyoderma gangrenosum.
- To synthesize available evidence on response rates and adverse events associated with interleukin inhibitor therapy for PG.
Main Methods:
- A comprehensive literature search was performed across major databases (PubMed, Embase, Scopus, Web of Science, Cochrane Library).
- Inclusion criteria focused on adult patients diagnosed with PG and treated with any interleukin inhibitor.
- Data from 60 papers involving 81 patients were analyzed.
Main Results:
- Interleukin inhibitor treatment demonstrated a 70% overall response rate and a 57% complete response rate in adult PG patients.
- Adverse events were infrequent (4%) and generally mild.
- Specific response rates varied: anakinra (59% response, 38% complete), canakinumab (64% response, 55% complete), and ustekinumab (79% response, 71% complete).
Conclusions:
- Off-label use of interleukin inhibitors is supported for managing recalcitrant pyoderma gangrenosum in adults due to observed efficacy and favorable safety profile.
- Publication bias may overestimate efficacy; further studies are required to compare different interleukin inhibitors and understand treatment response in relation to underlying conditions.
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