Efficacy of Biologics for Hidradenitis Suppurativa: A Network Meta Analysis and Meta Regression for Baseline Disease Severity

医学 化脓性汗腺炎 优势比 阿达木单抗 内科学 荟萃分析 可能性 元回归 临床试验 疾病严重程度 塞库金单抗 频数推理 子群分析 置信区间 英夫利昔单抗 逻辑回归 物理疗法 外科 诊断优势比 疾病 梅德林 随机对照试验
作者
James P. Pham,Tara Sholji,Marra Aghajani,Ericka Maye,Kate Burrell,Cindy Kok,John W. Frew
出处
期刊:Australasian Journal of Dermatology [Wiley]
标识
DOI:10.1111/ajd.70085
摘要

Hidradenitis Suppurativa is a challenging, heterogeneous inflammatory skin disease, with three approved biologic therapies. No head-to-head studies exist comparing these therapeutic modalities, and previous work has identified the influence of baseline disease severity upon clinical response. We aimed to perform a network meta-analysis of approved biologic therapies and meta-regression of baseline disease severity in moderate to severe HS. Pubmed, Embase, and Web of Science were searched from their inception up until 31 July 2025. Randomised Phase 3 clinical trials of biologic therapies approved for use in moderate to severe Hidradenitis Suppurativa. Network meta-analysis was conducted via both frequentist and Bayesian frameworks. Subgroup analysis was performed using a priori identified covariates (baseline AN count, tunnel count, BMI, and smoking), and random effects meta regression was performed with the final model selected using restricted maximum likelihood, I2, and Cochran's Q statistic. Adjusted odds ratios were then calculated. Efficacy outcomes analysed were the Hidradenitis Suppurativa Clinical Response (HiSCR-50) score, compared using odds ratios and 95% CI for frequentist analysis and odds ratio and 95% CrI for Bayesian methods. Adalimumab (OR = 2.81 95% CI 2.01-3.92), followed by Bimekizumab q2weekly (OR 2.24, 95% CI 1.52-3.29) had the highest odds of HiSCR50 clinical response compared to placebo. Baseline tunnel count was the only significant covariate influencing odds of response (OR = 0.225, 95% CI = 0.013-0.436, p = 0.0375), with meta-regression and adjusted odds ratios accounting for baseline tunnels demonstrating an increase in the odds of clinical response to Adalimumab and Bimekizumab, whilst the odds of achieving clinical response to Secukinumab became non-significant relative to placebo.
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