David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
Department of Dermatology, University of California Los Angeles, Los Angeles, California, USA.
Dermatol Ther. 2022 Sep;35(9):e15691. doi: 10.1111/dth.15691. Epub 2022 Jul 18.
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.
化脓性汗腺炎(HS)是一种慢性炎症性疾病,通常对治疗有抵抗力。目前缺乏关于英夫利昔单抗在 HS 中的应用的最新系统数据综述。我们对 HS 中使用英夫利昔单抗的文献进行了系统回顾和荟萃分析。本研究遵循系统评价和荟萃分析的首选报告项目以及在 PROSPERO(CRD42021283596)上进行了预注册。2021 年 9 月,系统地检索了 MEDLINE 和 EMBASE 上关于 HS 中使用英夫利昔单抗的文章。排除非英语、重复和<5 例 HS 患者的研究。利用 Cochrane 前瞻性试验风险偏倚和纽卡斯尔-渥太华量表评估研究质量。采用随机效应荟萃分析模型、Cochran's Q 统计量和 I 平方指数进行分析。19 篇文章(314 例患者)符合纳入标准(6 项前瞻性研究,13 项回顾性研究)。所有可获得 HS 严重程度数据的患者(n=299)均患有中重度疾病。荟萃分析中用于汇总反应率的结局测量主要基于临床医生报告的结局(16 项研究)。一项研究同时使用了临床医生和患者评估。两项研究仅使用患者报告的反应。英夫利昔单抗治疗 HS 患者的总体反应率为 83%(95%CI,0.71-0.91)。最常见的不良事件(AE)包括非严重感染(13.2%)和输注反应(2.9%)。严重 AE 的发生率为 2.9%。研究局限性包括前瞻性研究数量少和研究之间的异质性。总体而言,英夫利昔单抗是治疗中重度 HS 的有效药物。英夫利昔单抗在 HS 中的疗效应在更大的随机对照试验中与其他生物制剂进行比较。