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Infliximab in hidradenitis suppurativa: A systematic review and meta-analysis.
Shih, Terri; Lee, Katrina; Grogan, Tristan; De, Devea R; Shi, Vivian Y; Hsiao, Jennifer L.
Affiliation
  • Shih T; David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
  • Lee K; Department of Dermatology, University of California Los Angeles, Los Angeles, California, USA.
  • Grogan T; Department of Medicine Statistics Core, David Geffen School of Medicine, University of California, Los Angeles, California, USA.
  • De DR; Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York, USA.
  • Shi VY; Department of Dermatology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
  • Hsiao JL; Department of Dermatology, University of Southern California, Los Angeles, California, USA.
Dermatol Ther ; 35(9): e15691, 2022 09.
Article in En | MEDLINE | ID: mdl-35790062
ABSTRACT
Hidradenitis suppurativa (HS) is a chronic inflammatory often recalcitrant to treatment. There is a lack of an updated systematic data review for infliximab use in HS. We conducted a systematic review and meta-analysis of literature on infliximab in HS. This study was performed following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines and was pre-registered on PROSPERO (CRD42021283596). In 9/2021, MEDLINE and EMBASE were systematically searched for articles on infliximab in HS. Non-English, duplicate, and studies with <5 HS patients were excluded. Study quality was assessed utilizing Cochrane Risk of Bias for prospective trials and Newcastle-Ottawa Scale for cohort studies. Random effects meta-analytical model, Cochran's Q statistic, and I squared index were performed. Nineteen articles (314 patients) met inclusion criteria (six prospective, 13 retrospective studies). All patients with HS severity data available (n = 299) had moderate-to-severe disease. Outcome measures used for meta-analysis of the pooled response rate were largely based on clinician reported outcomes (16 studies). One utilized both clinician and patient assessment. Two utilized patient-reported response alone. The pooled response rate of HS patients to infliximab was 83% (95% CI, 0.71-0.91). The most common adverse events (AEs) included non-serious infections (13.2%) and infusion reaction (2.9%). The rate of serious AEs was 2.9%. Study limitations include the small number of prospective studies and heterogeneity between studies. Overall, infliximab is an effective treatment for moderate-to-severe HS. Efficacy of infliximab in HS should be compared to other biologics in larger, randomized controlled trials.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hidradenitis Suppurativa Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Dermatol Ther Journal subject: DERMATOLOGIA Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hidradenitis Suppurativa Type of study: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Dermatol Ther Journal subject: DERMATOLOGIA Year: 2022 Document type: Article Affiliation country: Estados Unidos