Husein-ElAhmed Husein, Husein-ElAhmed Sara
Department of Dermatology, Hospital de Baza, Granada, Spain.
Department of Dermatology, Montefrío Health Center, Andalusian Health Service, C. Mariana Pineda, Granada, Spain.
Indian J Dermatol Venereol Leprol. 2024 Feb 28:1-9. doi: 10.25259/IJDVL_665_2023.
Background Hidradenitis suppurativa (HS) is a challenging inflammatory skin condition. Recently, many different biologics have been tested for HS, but the paucity of head-to-head comparative trials makes it difficult to determine the real value of each biological intervention. We aimed to determine the relative efficacy among biologics in treating moderate-to-severe HS throughout a network meta-analysis (NMA) and, to identify which pathogenetic pathways may be the most appropriate to target. Methods We comprehensively identified studies in 3 databases and clinicaltrials.gov. The eligibility criteria included randomised controlled trials (RCTs) reporting data on the efficacy of moderate-to-severe HS. Results The NMA comprised 13 studies comprising 14 interventions on 2,748 participants in the network. The NMA showed the odds of achieving the clinical response were significantly superior with adalimumab (RR: 0.37, 95% CI = 0.06-0.63), adalimumab QW (RR: 0.63, 95% CI = 0.43-0.87), MAB1p (RR: 1.33, 95% CI = 0.03-3.12), secukinumab (RR: 0.25, 95% CI = 0.11-0.47) and secukinumabQ2W (RR: 0.24, 95% CI = 0.1-0.46) compared to placebo. Conclusion Based on the NMA, inhibiting tumour necrosis factor (TNF)-a with adalimumab appears to be the best strategy, followed by the blockade of IL--17 with secukinumab. Data for bimekizumab and CJM112 are promising. Infliximab has inconsistent clinical response, and more data are necessary to confirm this molecule as a potential third-line therapy in HS. The blockade of IL-23 and CD5a pathways is not relevant, or at least the current evidence is insufficient to recommend further investigation of guselkumab, risankizumab, and vilobelimab in phase III trials.
化脓性汗腺炎(HS)是一种具有挑战性的炎症性皮肤病。最近,许多不同的生物制剂已在HS中进行了测试,但缺乏头对头的比较试验使得难以确定每种生物干预的实际价值。我们旨在通过网络荟萃分析(NMA)确定生物制剂在治疗中度至重度HS中的相对疗效,并确定哪些致病途径可能是最适合靶向的。方法:我们全面检索了3个数据库和ClinicalTrials.gov中的研究。纳入标准包括报告中度至重度HS疗效数据的随机对照试验(RCT)。结果:NMA包括13项研究,涉及网络中的2748名参与者的14种干预措施。NMA显示,与安慰剂相比,阿达木单抗(RR:0.37,95%CI = 0.06-0.63)、阿达木单抗每周一次(RR:0.63,95%CI = 0.43-0.87)、MAB1p(RR:1.33,95%CI = 0.03-3.12)、司库奇尤单抗(RR:0.25,95%CI = 0.11-0.47)和司库奇尤单抗每2周一次(RR:0.24,95%CI = 0.1-0.46)实现临床反应的几率显著更高。结论:基于NMA,用阿达木单抗抑制肿瘤坏死因子(TNF)-α似乎是最佳策略,其次是用司库奇尤单抗阻断IL-17。比美吉珠单抗和CJM112的数据很有前景。英夫利昔单抗的临床反应不一致,需要更多数据来确认该分子作为HS潜在三线治疗的地位。阻断IL-23和CD5a途径不相关,或者至少目前的证据不足以推荐在III期试验中进一步研究古塞库单抗、瑞莎珠单抗和维洛贝单抗。