Tildrakizumab治疗中重度斑块型银屑病患者的回顾性分析:真实临床数据

Q3 Medicine
Nancy W Wei, Sunny Chi, Mark G Lebwohl
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引用次数: 0

摘要

背景:白细胞介素(IL)-23拮抗剂在治疗中重度斑块型银屑病的临床试验数据中显示出良好的疗效和最小的副作用。到目前为止,还没有关于接受替德拉基单抗治疗的真实世界患者的公布数据。目的:分析替德拉基单抗治疗中重度斑块型银屑病的真实疗效和安全性。方法:在一家大型城市学术医疗中心对所有接受替拉单抗治疗的中重度斑块型银屑病患者进行回顾性图表审查。收集并统计分析了首次就诊和12个月随访的人口学信息、银屑病面积和严重程度指数(PASI)、合并症和任何可能的不良事件。结果:30例接受替拉单抗治疗的患者被纳入分析。总体而言,初次访视时PASI的平均值±标准差为15.8±11.8,12个月随访时为1.5±2.9(P<.001)。未报告严重不良事件。结论:Tildrakizumab在临床试验和这个现实世界的队列中显示出治疗中重度斑块型银屑病的疗效,具有良好的安全性。未来应进行研究,以评估替拉单抗与其他IL-23抑制剂的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retrospective Analysis in Patients With Moderate to Severe Plaque Psoriasis Treated With Tildrakizumab: Real-Life Clinical Data.

Background: Interleukin (IL)-23 antagonists have shown great efficacy with minimal side effect profile in clinical trial data for the treatment of moderate to severe plaque psoriasis. As of yet, there have been no published data regarding real-world patients who have received tildrakizumab therapy. Objectives: To analyze real-world efficacy and safety of tildrakizumab in patients with moderate to severe plaque psoriasis. Methods: A retrospective chart review was performed at a large urban academic medical center for all patients treated with tildrakizumab for moderate to severe plaque psoriasis. Demographic information, Psoriasis Area and Severity Indexs(PASIs) from initial presentation and 12-month follow-up, comorbidities, and any possible adverse events were collected and analyzed statistically. Results: 30 patients on tildrakizumab therapy were included in the analysis. Overall, the mean ± standard deviation of the PASIs was 15.8 ± 11.8 at initial visit and 1.5 ± 2.9 at 12-month follow-up (P < .001). No serious adverse events were reported. Conclusions: Tildrakizumab has shown efficacy in clinical trials and this real-world cohort for the treatment of moderate to severe plaque psoriasis with a good safety profile. Future studies should be done to assess the efficacy of tildrakizumab compared with other IL-23 inhibitors.

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CiteScore
1.30
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