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高剂量、高频度英夫利昔单抗:治疗化脓性汗腺炎的一种新治疗模式。

High-dose, high-frequency infliximab: A novel treatment paradigm for hidradenitis suppurativa.

机构信息

Division of Dermatology, Department of Internal Medicine, Albert Einstein College of Medicine, Bronx, New York.

Departments of Dermatology and Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

J Am Acad Dermatol. 2020 May;82(5):1094-1101. doi: 10.1016/j.jaad.2019.09.071. Epub 2019 Oct 4.

Abstract

BACKGROUND

The permanent disfigurement associated with hidradenitis suppurativa (HS) necessitates early aggressive disease intervention. Although limited data support the use of infliximab (IFX) in HS, the efficacy of high-dose, high-frequency IFX has yet to be defined.

OBJECTIVE

To evaluate the efficacy of IFX 7.5 to 10 mg/kg, with a maintenance frequency every 4 weeks.

METHODS

Prospective analysis of 42 patients initiating IFX 7.5 mg/kg every 4 weeks (IFX 7.5) and 16 patients receiving dose escalation to IFX 10 mg/kg every 4 weeks (IFX 10) between March 1, 2018, and February 28, 2019. The primary outcome measure (clinical response) was the proportion of patients with Physician Global Assessment of clear, minimal, or mild (score of 0-2) HS with at least a 2-grade improvement from baseline scores.

RESULTS

The proportion of patients achieving a clinical response after initiating IFX 7.5 was 20 of 42 (47.6%) at week 4 and 17 of 24 (70.8%) at week 12. For patients receiving dose escalation to IFX 10 because of incomplete initial response, 6 of 16 (37.5%) achieved clinical response at week 4 and 6 of 12 (50%) at week 12.

CONCLUSIONS

Initiation of IFX 7.5 every 4 weeks, with possible dose escalation to IFX 10, if needed, provides optimal mitigation of HS-related disease activity.

摘要

背景

化脓性汗腺炎(HS)导致的永久性毁容需要早期积极的疾病干预。尽管有限的数据支持英夫利昔单抗(IFX)在 HS 中的应用,但高剂量、高频率 IFX 的疗效尚未确定。

目的

评估每 4 周给予 7.5 至 10 mg/kg 的 IFX 的疗效,维持频率为每 4 周一次。

方法

前瞻性分析了 42 例于 2018 年 3 月 1 日至 2019 年 2 月 28 日期间开始每 4 周给予 7.5 mg/kg IFX(IFX 7.5)的患者和 16 例剂量递增至每 4 周给予 10 mg/kg IFX(IFX 10)的患者。主要结局指标(临床反应)是指与基线评分相比至少有 2 级改善的患者比例,这些患者的医师整体评估 HS 为清晰、轻微或轻度(评分为 0-2)。

结果

在开始 IFX 7.5 后第 4 周,有 20/42(47.6%)例患者达到临床反应,第 12 周时为 17/24(70.8%)例。对于因初始反应不完全而接受 IFX 10 剂量递增的患者,第 4 周时 6/16(37.5%)例达到临床反应,第 12 周时 6/12(50%)例达到临床反应。

结论

每 4 周开始给予 IFX 7.5,并在需要时可能递增至 IFX 10,可最佳缓解 HS 相关疾病活动。

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