Wei Nancy W, Chi Sunny, Lebwohl Mark G
The Kimberly and Eric J. Waldman Department of Dermatology, Icahn School of Medicine at Mount Sinai Hospital, New York, NY, USA.
J Psoriasis Psoriatic Arthritis. 2022 Apr;7(2):55-59. doi: 10.1177/24755303221077211. Epub 2022 Mar 29.
: 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. : To analyze real-world efficacy and safety of tildrakizumab in patients with moderate to severe plaque psoriasis. : 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. : 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. : 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.
白细胞介素(IL)-23拮抗剂在中度至重度斑块状银屑病治疗的临床试验数据中显示出巨大疗效且副作用极小。截至目前,尚无关于接受替拉珠单抗治疗的真实世界患者的已发表数据。
分析替拉珠单抗在中度至重度斑块状银屑病患者中的真实世界疗效和安全性。
在一家大型城市学术医疗中心对所有接受替拉珠单抗治疗中度至重度斑块状银屑病的患者进行回顾性病历审查。收集人口统计学信息、初始就诊时和12个月随访时的银屑病面积和严重程度指数(PASI)、合并症以及任何可能的不良事件,并进行统计学分析。
30例接受替拉珠单抗治疗的患者纳入分析。总体而言,初始就诊时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。
替拉珠单抗在临床试验和该真实世界队列中对中度至重度斑块状银屑病的治疗显示出疗效,且安全性良好。未来应开展研究以评估替拉珠单抗与其他IL-23抑制剂相比的疗效。