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拓展化脓性汗腺炎治疗选择的前沿:比美吉珠单抗的有效贡献。

Expanding the frontiers of therapeutic options in hidradenitis suppurativa: The valid contribution of bimekizumab.

机构信息

Dermatological Unit, Department of Clinical and Molecular Sciences, Polytechnic Marche University, Ancona, Italy.

Dermatological Unit, Department of Clinical and Molecular Sciences, Polytechnic Marche University, Ancona, Italy.

出版信息

Med. 2024 Oct 11;5(10):1197-1199. doi: 10.1016/j.medj.2024.08.005.

DOI:10.1016/j.medj.2024.08.005
PMID:39395402
Abstract

Hidradenitis suppurativa (HS) is a chronic inflammatory cutaneous disorder with a significant negative impact on quality of life. Th17 axis has a central role in the pathogenesis of HS. Kimball et al. demonstrated the efficacy and safety of bimekizumab in two double-blind, placebo-controlled phase 3 studies (BE HEARD I-II), adding a new targeting option to the therapeutic armamentarium of HS..

摘要

化脓性汗腺炎(HS)是一种慢性炎症性皮肤病,对生活质量有重大负面影响。Th17 轴在 HS 的发病机制中起核心作用。Kimball 等人在两项双盲、安慰剂对照的 3 期研究(BE HEARD I-II)中证明了 bimekizumab 的疗效和安全性,为 HS 的治疗手段增添了一种新的靶向选择。

相似文献

1
Expanding the frontiers of therapeutic options in hidradenitis suppurativa: The valid contribution of bimekizumab.拓展化脓性汗腺炎治疗选择的前沿:比美吉珠单抗的有效贡献。
Med. 2024 Oct 11;5(10):1197-1199. doi: 10.1016/j.medj.2024.08.005.
2
Efficacy and safety of bimekizumab in patients with moderate-to-severe hidradenitis suppurativa (BE HEARD I and BE HEARD II): two 48-week, randomised, double-blind, placebo-controlled, multicentre phase 3 trials.比美吉珠单抗治疗中重度化脓性汗腺炎患者的疗效和安全性(BE HEARD I 和 BE HEARD II):两项为期 48 周、随机、双盲、安慰剂对照、多中心 3 期临床试验。
Lancet. 2024 Jun 8;403(10443):2504-2519. doi: 10.1016/S0140-6736(24)00101-6. Epub 2024 May 22.
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Bimekizumab for the treatment of hidradenitis suppurativa.比美吉珠单抗治疗化脓性汗腺炎。
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Efficacy and Safety of Bimekizumab in Moderate to Severe Hidradenitis Suppurativa: A Phase 2, Double-blind, Placebo-Controlled Randomized Clinical Trial.比美吉珠单抗治疗中重度化脓性汗腺炎的疗效和安全性:一项 2 期、双盲、安慰剂对照随机临床试验。
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Secukinumab in patients with moderate-to-severe hidradenitis suppurativa based on prior biologic exposure: an efficacy and safety analysis from the SUNSHINE and SUNRISE phase III trials.基于既往生物制剂暴露情况的中重度化脓性汗腺炎患者使用司库奇尤单抗:来自 III 期 SUNSHINE 和 SUNRISE 研究的疗效和安全性分析。
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Secukinumab in moderate-to-severe hidradenitis suppurativa (SUNSHINE and SUNRISE): week 16 and week 52 results of two identical, multicentre, randomised, placebo-controlled, double-blind phase 3 trials.司库奇尤单抗治疗中重度化脓性汗腺炎(SUNSHINE和SUNRISE研究):两项相同的多中心、随机、安慰剂对照、双盲3期试验的第16周和第52周结果
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Assessing the validity, responsiveness and meaningfulness of the Hidradenitis Suppurativa Clinical Response (HiSCR) as the clinical endpoint for hidradenitis suppurativa treatment.评估化脓性汗腺炎临床应答(HiSCR)作为化脓性汗腺炎治疗的临床终点的有效性、反应性和有意义性。
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引用本文的文献

1
IRAK4 Targeting: A Breakthrough Approach to Combat Hidradenitis Suppurativa.靶向IRAK4:治疗化脓性汗腺炎的突破性方法。
Biologics. 2025 Jun 30;19:387-397. doi: 10.2147/BTT.S525106. eCollection 2025.