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阿达木单抗与甲氨蝶呤和安慰剂治疗中度至重度银屑病的获益-风险分析:CHAMPION 试验中不良反应无事件天数的比较。

Benefit-risk analysis of adalimumab versus methotrexate and placebo in the treatment of moderate to severe psoriasis: comparison of adverse event-free response days in the CHAMPION trial.

机构信息

Dermatologikum Hamburg, Hamburg, Germany.

出版信息

J Am Acad Dermatol. 2010 Dec;63(6):1011-8. doi: 10.1016/j.jaad.2009.12.029. Epub 2010 Oct 8.

DOI:10.1016/j.jaad.2009.12.029
PMID:20933301
Abstract

BACKGROUND

The Comparative Study of Humira versus Methotrexate (MTX) versus Placebo in Psoriasis Patients (CHAMPION) demonstrated superior efficacy of biologic over conventional systemic immunosuppressant therapy in psoriasis.

OBJECTIVE

We sought to compare the risk-benefit profile of adalimumab (ADA), MTX, and placebo using data from CHAMPION.

METHODS

Patients randomized to ADA (n = 107), MTX (n = 110), or placebo (n = 53) were followed up for 16 weeks. Response (≥75% improvement in Psoriasis Area and Severity Index), days free of adverse events (AEs), moderate to severe AEs, infection-related AEs, and study drug-related AEs were analyzed.

RESULTS

ADA treatment was associated with substantially more days (SD) of AE-free response compared with MTX or placebo treatment, respectively: 36.9 (31.1) versus 8.3 (15.9) or 6.7 (18.1) days of response free of any AEs, 43.8 (31.9) versus 11.1 (19.9) or 7.9 (19.9) days of response free of moderate to severe AEs, 48.5 (29.2) versus 12.4 (21.7) or 9.2 (21.8) days of response free of infection-related AEs, and 44.6 (31.4) versus 11.8 (21.1) or 10.0 (24.0) days free of study drug-related AEs (all P < .0001 for ADA vs MTX or placebo).

LIMITATIONS

This clinical trial-based analysis may not have captured the full spectrum of AEs in the actual clinical setting. The short (16-week) duration of the trial limited the ability to capture some important but uncommon AEs associated with long-term ADA or MTX use.

CONCLUSION

With 4 times as many AE-free response days, ADA demonstrated a superior benefit-risk profile.

摘要

背景

在银屑病患者中 Humira 对比甲氨蝶呤(MTX)对比安慰剂的比较研究(CHAMPION)表明生物制剂比传统的全身免疫抑制剂治疗银屑病更有效。

目的

我们试图使用 CHAMPION 的数据来比较阿达木单抗(ADA)、MTX 和安慰剂的风险效益比。

方法

107 名接受 ADA 治疗、110 名接受 MTX 治疗和 53 名接受安慰剂治疗的患者接受了 16 周的随访。分析了应答(Psoriasis Area and Severity Index 改善≥75%)、无不良事件(AE)天数、中重度 AE、感染相关 AE 和研究药物相关 AE。

结果

ADA 治疗与 MTX 或安慰剂治疗相比,无 AE 应答天数显著增加:无任何 AE 的应答天数分别为 36.9(31.1)、8.3(15.9)或 6.7(18.1)天,无中重度 AE 的应答天数分别为 43.8(31.9)、11.1(19.9)或 7.9(19.9)天,无感染相关 AE 的应答天数分别为 48.5(29.2)、12.4(21.7)或 9.2(21.8)天,无研究药物相关 AE 的应答天数分别为 44.6(31.4)、11.8(21.1)或 10.0(24.0)天(所有 P <.0001 均为 ADA 与 MTX 或安慰剂比较)。

局限性

基于临床试验的分析可能没有捕捉到实际临床环境中的所有 AE 谱。试验的短期(16 周)限制了捕捉一些与长期 ADA 或 MTX 使用相关的重要但罕见的 AE 的能力。

结论

ADA 具有 4 倍的无 AE 应答天数,表现出更好的风险效益比。

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