首页> 外文期刊>Journal of the European Academy of Dermatology and Venereology: JEADV >Tildrakizumab efficacy and impact on quality of life up to 52 weeks in patients with moderate‐to‐severe psoriasis: a pooled analysis of two randomized controlled trials
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Tildrakizumab efficacy and impact on quality of life up to 52 weeks in patients with moderate‐to‐severe psoriasis: a pooled analysis of two randomized controlled trials

机译:中度至严重的牛皮癣患者的患者疗效和对生命质量的疗效和影响:两种随机对照试验的汇总分析

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Abstract Background Two randomized controlled trials (reSURFACE 1 and 2) have demonstrated the effectiveness of tildrakizumab, a high‐affinity, humanized, IgG1κ, anti‐interleukin‐23 monoclonal antibody, for treating moderate‐to‐severe plaque psoriasis in the first 28?weeks. Objectives To examine the efficacy of tildrakizumab and its impact on quality of life (QoL) in patients with different levels of week‐28 Psoriasis Area and Severity Index (PASI) improvement. Methods Patients treated with tildrakizumab 100?mg or 200?mg from baseline to week 28 were pooled from reSURFACE 1 and reSURFACE 2 and classified into five mutually exclusive week‐28 PASI improvement groups for each dose: PASI 0–49, 50–74, 75–89, 90–99 and 100. Mean PASI improvement and Dermatology Life Quality Index (DLQI) 0/1 over time were examined for each group. Results Of 1156 patients, 575 were in the 100‐mg and 578 in the 200‐mg cohorts, respectively. At week 28, 8.3%, 14.3%, 23.8%, 30.4% and 23.1% in the 100‐mg and 4.0%, 18.1%, 19.6%, 29.1% and 29.3% in the 200‐mg cohort achieved PASI??50, 50–74, 75–89, 90–99 and 100, respectively. Patients with PASI??50 at week 28 could be identified as early as week 8, and those with week‐28 PASI?≥?90 had approximately 50% PASI improvement by week 4. Among patients achieving PASI??50 at week 28 who continued the same dose of tildrakizumab to week 52, mean PASI improvement was maintained or improved over time. Similar results were observed for both doses. Higher proportions of patients achieved DLQI 0/1 in higher week‐28 PASI groups, and DLQI 0/1 was maintained or improved to week 52. However, not all patients with PASI 100 had DLQI 0/1. Conclusion Patients unlikely to respond to tildrakizumab could be identified by week 8, and those likely to achieve a PASI?≥?90 response could be identified as early as week 4. Week‐28 PASI improvement level correlated with QoL improvement.
机译:摘要背景下两项随机对照试验(Resurface 1和2)已经证明了Tiantrokizumab,高亲和力,人源化,IgG1κ,抗白细胞介素-33单克隆抗体的有效性,用于治疗前28中的中度至严重的斑块牛皮癣?周。目的考察Tildrokizumab的疗效及其对患有不同水平的牛皮癣面积和严重程度指数(PASI)改进患者的患者的生命质量(QOL)的影响。方法从基线到第28周,从Resurface 1和Resurface 2汇集了患有TiNIDrakizumab 100的患者的患者从基线到第28周,并分为每次剂量的五个相互关联的周-28促进群体:PASI 0-49,50-74, 75-89,90-99和100.每个组检查平均促进和皮肤病学生活质量指数(DLQI)0/1。结果1156名患者,575例分别在100毫克和578中,分别为200毫克队列。在200mg和4.0%,18.1%,19.6%,200mg队列中的8.3%,14.3%,23.8%,30.4%和23.1%,18.1%,19.6%,29.1%和29.3%所达到的PASIα,18.1%,19.6%,29.1%和29.3%。分别为50,50-74,75-89,90-99和100。患者患者患者在第28周的第28周,每周8节和第28周的那些患者可以鉴定出一周 - 28 = 90的患者,每周有大约50%的PASI提高。在第28周,持续相同剂量的Tiandrokizumab至第52周,随着时间的推移,保持或改善了平均促进性。两种剂量观察到类似的结果。较高比例的患者在较高的一周-28帕西基组中获得DLQI 0/1,并且DLQI 0/1维持或改善至第52周。然而,并非所有患有DLQI 0/1的患者。结论可能在第8周可以识别不太可能对Tiantrokizumab进行响应的患者,并且可能达到PASI的那些可能会尽早识别出现PASI的响应4.周-28 PASI改善水平与QOL改善相关。

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