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Efficacy of anti-interleukin-17A biological agents for palmoplantar psoriasis and palmoplantar pustulosis: A network meta-analysis.
Xia, RuiYuan; Diao, ZiYue; Chen, DanDan; Wang, YuFei; Zhou, ChaoJing; Gao, YaMei; Yin, ZhiQiang.
Afiliação
  • Xia R; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Diao Z; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Chen D; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Wang Y; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Zhou C; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Gao Y; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
  • Yin Z; Department of Dermatology, First Affiliated Hospital of Nanjing Medical University, Nanjing, China. Electronic address: yinzhiqiang@njmu.edu.cn.
Int Immunopharmacol ; 130: 111716, 2024 Mar 30.
Article em En | MEDLINE | ID: mdl-38417367
ABSTRACT

BACKGROUND:

The comparative efficacy of anti-IL (interleukin)-17A biological agents in palmoplantar psoriasis (PP) and palmoplantar pustulosis (PPP) are not well established.

OBJECTIVE:

To investigate the efficacy of different dosage regimens of anti-IL-17A biological agents compared with placebo in PP and PPP.

METHODS:

A literature search was conducted in PubMed, clinicaltrials.gov, and Embase. Meta-analysis was performed for all outcomes of randomized controlled trials, while network meta-analysis was only performed for the primary outcome.

RESULTS:

In total, 21 articles exploring the efficacy of 5 treatment options were included, 4 cohort studies were also reviewed. Meta-analysis demonstrated a statistically significant difference favoring anti-IL-17A biological agents versus placebo (OR = 6.84, 95 %[CI] [5.34, 8.76]). On-label secukinumab was identified as the most effective treatment option for patients with PP (OR = 33.50, 95 %[CI] [4.37,256.86]). PPP treated with secukinumab 300 mg showed benefit in terms of PPPASI 75 responses over 52 weeks.

CONCLUSION:

IL-17A biological agents had better PP disease clearance compared with placebo and on-label secukinumab was identified as the most effective treatment option for PP patients. Secukinumab 300 mg showed benefit for PPP patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Psoríase / Interleucina-17 Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Psoríase / Interleucina-17 Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article