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比较中重度银屑病生物制剂的网络荟萃分析所需治疗人数

Number Needed to Treat Network Meta-Analysis to Compare Biologic Drugs for Moderate-to-Severe Psoriasis.

机构信息

Saint Louis University School of Medicine, St. Louis, MO, USA.

Eli Lilly and Company, Indianapolis, IN, USA.

出版信息

Adv Ther. 2022 May;39(5):2256-2269. doi: 10.1007/s12325-022-02065-w. Epub 2022 Mar 22.


DOI:10.1007/s12325-022-02065-w
PMID:35316500
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9056462/
Abstract

INTRODUCTION: Number needed to treat (NNT) estimates are a practical metric to help identify the most effective therapies. Our objective is to compare 11 biologic drugs for moderate-to-severe psoriasis in terms of NNT. METHODS: The NNT data were obtained from a Bayesian network meta-analysis of 42 double-blind, randomized, phase 3 clinical trials for 11 biologics (adalimumab, brodalumab, certolizumab pegol, etanercept, guselkumab, infliximab, ixekizumab, risankizumab, secukinumab, tildrakizumab, and ustekinumab). We determined NNT to achieve Psoriasis Area and Severity Index (PASI) 75/90/100 responses at weeks 4, 8, 12, 16, and 48/52 and Dermatology Life Quality Index (DLQI) response 0, 1 at week 12. RESULTS: Highest efficacy (lowest NNT) was with brodalumab and ixekizumab for PASI 90 at weeks 4, 8, and 12; ixekizumab for PASI 90/100 at week 16; and brodalumab for PASI 100 at week 12. After 48/52 weeks, risankizumab had the highest efficacy for PASI 90/100 overlapping with guselkumab, brodalumab, and ixekizumab for PASI 90 and with brodalumab and ixekizumab for PASI 100. Ixekizumab had the highest efficacy for DLQI (0,1) at week 12. CONCLUSIONS: Brodalumab and ixekizumab had the lowest NNTs for achieving PASI responses at early time points and were not significantly different than risankizumab and guselkumab after 48/52 weeks.

摘要

简介:需要治疗的人数 (NNT) 估计是一种实用的指标,可以帮助确定最有效的治疗方法。我们的目的是比较 11 种用于中度至重度银屑病的生物药物的 NNT。

方法:NNT 数据来自对 11 种生物制剂(阿达木单抗、布罗达umab、依那西普、古塞库单抗、英夫利昔单抗、依奇珠单抗、瑞莎珠单抗、司库奇尤单抗、特诺利珠单抗、乌司奴单抗和替西珠单抗)的 42 项双盲、随机、3 期临床试验的贝叶斯网络荟萃分析。我们确定了在第 4、8、12、16 周和第 48/52 周达到银屑病面积和严重程度指数 (PASI) 75/90/100 反应以及在第 12 周达到皮肤病生活质量指数 (DLQI) 0、1 反应的 NNT。

结果:阿达木单抗和依奇珠单抗在第 4、8 和 12 周时对 PASI 90 的疗效最高(NNT 最低);依奇珠单抗在第 16 周时对 PASI 90/100 的疗效最高;布罗达单抗在第 12 周时对 PASI 100 的疗效最高。第 48/52 周后,瑞莎珠单抗对 PASI 90/100 的疗效最高,与古塞库单抗、布罗达单抗和依奇珠单抗的 PASI 90 重叠,与布罗达单抗和依奇珠单抗的 PASI 100 重叠。依奇珠单抗在第 12 周时对 DLQI(0,1)的疗效最高。

结论:布罗达单抗和依奇珠单抗在早期时间点达到 PASI 反应的 NNT 最低,与第 48/52 周后的瑞莎珠单抗和古塞库单抗无显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/e7d97adcf3f2/12325_2022_2065_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/17b2b52c35c5/12325_2022_2065_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/1abcf37eba09/12325_2022_2065_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/1c8148224d32/12325_2022_2065_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/e7d97adcf3f2/12325_2022_2065_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/17b2b52c35c5/12325_2022_2065_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/1abcf37eba09/12325_2022_2065_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/1c8148224d32/12325_2022_2065_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a808/9056462/e7d97adcf3f2/12325_2022_2065_Fig4_HTML.jpg

相似文献

[1]
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[2]
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[6]
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[7]
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[3]
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[4]
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[5]
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[6]
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Front Immunol. 2023

[7]
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[8]
[Not Available].

Glob Reg Health Technol Assess. 2022-11-10

[9]
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本文引用的文献

[1]
Comparative Efficacy and Relative Ranking of Biologics and Oral Therapies for Moderate-to-Severe Plaque Psoriasis: A Network Meta-analysis.

Dermatol Ther (Heidelb). 2021-6

[2]
A head-to-head comparison of ixekizumab vs. guselkumab in patients with moderate-to-severe plaque psoriasis: 24-week efficacy and safety results from a randomized, double-blinded trial.

Br J Dermatol. 2021-6

[3]
Efficacy and Safety of Continuous Risankizumab Therapy vs Treatment Withdrawal in Patients With Moderate to Severe Plaque Psoriasis: A Phase 3 Randomized Clinical Trial.

JAMA Dermatol. 2020-6-1

[4]
Targeted therapies for patients with moderate-to-severe psoriasis: a systematic review and network meta-analysis of PASI response at 1 year.

J Dermatolog Treat. 2022-2

[5]
Comparison of Biologics and Oral Treatments for Plaque Psoriasis: A Meta-analysis.

JAMA Dermatol. 2020-3-1

[6]
Comparison of cumulative clinical benefits of biologics for the treatment of psoriasis over 16 weeks: Results from a network meta-analysis.

J Am Acad Dermatol. 2019-12-26

[7]
Rapid Response of Biologic Treatments of Moderate-to-Severe Plaque Psoriasis: A Comprehensive Investigation Using Bayesian and Frequentist Network Meta-analyses.

Dermatol Ther (Heidelb). 2020-2

[8]
Short-Term Efficacy and Safety of IL-17, IL-12/23, and IL-23 Inhibitors Brodalumab, Secukinumab, Ixekizumab, Ustekinumab, Guselkumab, Tildrakizumab, and Risankizumab for the Treatment of Moderate to Severe Plaque Psoriasis: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials.

J Immunol Res. 2019-9-10

[9]
Assessing the relative efficacy of interleukin-17 and interleukin-23 targeted treatments for moderate-to-severe plaque psoriasis: A systematic review and network meta-analysis of PASI response.

PLoS One. 2019-8-14

[10]
Guselkumab versus secukinumab for the treatment of moderate-to-severe psoriasis (ECLIPSE): results from a phase 3, randomised controlled trial.

Lancet. 2019-8-8

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