Application of the Statistical Method to Convert Published PASI 50/75/90/100 into Absolute PASI Response Rate in Patients with Moderate-to-Severe Plaque Psoriasis Treated with Tildrakizumab Based on Data from the Two Pivotal Phase 3 Studies reSURFACE 1 and reSURFACE 2.

Dermatology (Basel, Switzerland) Pub Date : 2022-01-01 Epub Date: 2022-02-15 DOI:10.1159/000522009
Igor Dykukha, Andreu Schoenenberger, Ismail Kasujee, Ulrich Mrowietz, Reinhard Vonthein
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引用次数: 0

Abstract

Background: Absolute Psoriasis Area and Severity Index (PASI) is a key endpoint in psoriasis management. Petto et al. [Pharm Stat. 2019;18(1):4-21] developed a statistical method to estimate the proportion of patients reaching absolute PASI response given baseline PASI score and proportion of patients achieving relative improvements at predefined time points.

Objectives: To test this method on clinical data from two phase 3 tildrakizumab trials (reSURFACE 1/2) comparing estimated absolute PASI ≤1/≤2/≤3/≤5 responses with reference responses from clinical databases.

Methods: Reference PASI responses of ≤1/≤2/≤3/≤5 were extracted from clinical databases. Estimation of absolute PASI ≤1/≤2/≤3/≤5 response rates at week (W) 12 and W28 by treatment and trial were performed. Differences between estimated and reference responses were analysed. Bland-Atman limits of agreement and Passing-Bablok regression to assess variations between estimated and reference responses were performed.

Results: Differences between estimated and reference absolute PASI ≤1/≤2/≤3/≤5 responses at W12 and W28 by treatment and trial were of little clinical relevance with an overall mean difference in PASI response proportion of -2.2% (e.g., for the tildrakizumab 100-mg arm, original proportions of patients achieving PASI of ≤1/≤2/≤3/≤5 at W28 were 38.5%/52.2%/63.5%/73.9% and 39.8%/54.8%/63.6%/76.9% [reSURFACE 1 and 2, respectively] vs. estimated proportions of 33.2%/49.8%/62.5%/78.3% and 34.3%/51.6%/64.5%/79.9%). Limits of agreement were -7.1% to 1.4% at W12 and -6.8% to 4.3% at W28. Scatterplots revealed linearity that stood the cusum test in Passing-Bablok regression with slope 1.14 (95% confidence intervals: 1.06 to 1.20).

Conclusion: Good estimates of absolute PASI response rates were achieved with the application of the statistical method to tildrakizumab data reported in the phase 3 studies, in particular in the verum study arms. Our data support the method provided by Petto et al. [2019] to estimate proportions of psoriasis patients reaching absolute PASI value thresholds using relative PASI improvements.

基于两项关键性3期研究reSURFACE 1和reSURFACE 2的数据,应用统计学方法将已发表的PASI 50/75/90/100转化为Tildrakizumab治疗中重度斑块性银屑病患者的绝对PASI缓解率
背景:绝对银屑病面积和严重程度指数(PASI)是银屑病治疗的关键指标。Petto等人[Pharm Stat. 2019;18(1):4-21]开发了一种统计方法来估计在给定基线PASI评分的情况下达到绝对PASI缓解的患者比例和在预定义时间点达到相对改善的患者比例。目的:通过两项tildrakizumab 3期临床试验(reSURFACE 1/2)的临床数据来检验该方法,比较估计的绝对PASI≤1/≤2/≤3/≤5反应与临床数据库中的参考反应。方法:从临床数据库中提取≤1/≤2/≤3/≤5的参考PASI反应。通过治疗和试验估计第12周和第28周PASI≤1/≤2/≤3/≤5的绝对缓解率。分析了估计响应与参考响应的差异。进行Bland-Atman一致性极限和Passing-Bablok回归来评估估计反应和参考反应之间的差异。结果:治疗和试验在W12和W28时PASI≤1/≤2/≤3/≤5的估计和参考绝对反应之间的差异几乎没有临床相关性,PASI反应比例的总体平均差异为-2.2%(例如,对于tildrakizumab 100-mg组,在W28时达到PASI≤1/≤2/≤3/≤5的患者的原始比例分别为38.5%/52.2%/63.5%/73.9%和39.8%/54.8%/63.6%/76.9%)。预估比例分别为33.2%/49.8%/62.5%/78.3%和34.3%/51.6%/64.5%/79.9%)。W12和W28的协议上限分别为-7.1% - 1.4%和-6.8% - 4.3%。散点图显示线性符合passingbablok回归的cusum检验,斜率为1.14(95%置信区间为1.06 ~ 1.20)。结论:将统计学方法应用于3期研究中报告的tildrakizumab数据,特别是在verum研究组中,可以很好地估计绝对PASI缓解率。我们的数据支持Petto等人[2019]提供的方法,即使用相对PASI改善来估计达到绝对PASI值阈值的牛皮癣患者比例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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