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司库奇尤单抗在接受过大量治疗的银屑病患者中的生存情况:一项为期两年的单中心回顾性研究。

Ixekizumab Survival in Heavily Pretreated Patients with Psoriasis: A Two-year Single-centre Retrospective Study.

作者信息

Sherman Shany, Zloczower Ory, Noyman Yehonatan, Amitay-Laish Iris, Hodak Emmilia, Pavlovsky Lev

机构信息

Division of Dermatology, Rabin Medical Center - Beilinson Hospital, Petach Tikva 4941492, Israel.

出版信息

Acta Derm Venereol. 2020 Dec 14;100(19):adv00349. doi: 10.2340/00015555-3714.

DOI:10.2340/00015555-3714
PMID:33283248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9309699/
Abstract

The long-term effect of intra-anti-interleukin-17-class switch on drug survival is unclear. The aim of this study was to evaluate the efficacy and long-term survival of ixekizumab in bio-experienced psoriatic patients with and without previous exposure to anti-interleukin-17 treatment. Retrospective search of a tertiary medical centre database for 2017 to 2019 yielded 73 patients treated with ixekizumab: 50 previously exposed to secukinumab and 23 anti-interleukin-17-naïve. Median baseline Psoriasis Area Severity Index (PASI) was 23.0. Median number of received biologics was 4. Mean drug survival was 16.4 and 16.8 months in the anti-interleukin-17-exposed and naïve groups, respectively (p = 0.878). There was no between-group difference in proportion of patients achieving ≥ 75 PASI response. At study end, 25 anti-interleukin-17-exposed patients (50.0%) and 17 anti-interleukin-17-naïve patients (73.9%) were still on ixekizumab. The use of multiple previous biologic treatments was associated with substantially reduced ixekizumab survival. In conclusion, previous anti-interleukin-17-exposure was associated with an initially favourable response and did not further reduce ixekizumab survival.

摘要

抗白细胞介素-17类别转换对药物留存的长期影响尚不清楚。本研究的目的是评估司库奇尤单抗在有或无抗白细胞介素-17治疗史的生物制剂治疗经验丰富的银屑病患者中的疗效和长期留存情况。对一家三级医疗中心2017年至2019年数据库进行回顾性检索,筛选出73例接受司库奇尤单抗治疗的患者:50例曾接受过司库奇尤单抗治疗,23例未接受过抗白细胞介素-17治疗。银屑病面积和严重程度指数(PASI)基线中位数为23.0。接受生物制剂的中位数为4种。抗白细胞介素-17治疗组和未治疗组的平均药物留存时间分别为16.4个月和16.8个月(p = 0.878)。达到PASI改善≥75%的患者比例在两组之间无差异。在研究结束时,25例接受过抗白细胞介素-17治疗的患者(50.0%)和17例未接受过抗白细胞介素-17治疗的患者(73.9%)仍在使用司库奇尤单抗。既往使用多种生物制剂治疗与司库奇尤单抗留存率显著降低相关。总之,既往接受过抗白细胞介素-17治疗与初始良好反应相关,且未进一步降低司库奇尤单抗的留存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec9/9309699/42faf5e91b7c/ActaDV-100-19-5960-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec9/9309699/e81fa7f21042/ActaDV-100-19-5960-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec9/9309699/42faf5e91b7c/ActaDV-100-19-5960-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec9/9309699/e81fa7f21042/ActaDV-100-19-5960-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec9/9309699/42faf5e91b7c/ActaDV-100-19-5960-g002.jpg

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本文引用的文献

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Efficacy of a second interleukin 17 inhibitor in patients with psoriasis: A systematic review and meta-analysis.银屑病患者中第二种白细胞介素 17 抑制剂的疗效:系统评价和荟萃分析。
J Am Acad Dermatol. 2021 Jan;84(1):130-138. doi: 10.1016/j.jaad.2020.07.085. Epub 2020 Jul 28.
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Comparison of real-world treatment patterns among patients with psoriasis prescribed ixekizumab or secukinumab.比较依奇珠单抗或司库奇尤单抗治疗银屑病患者的真实世界治疗模式。
J Am Acad Dermatol. 2020 Apr;82(4):927-935. doi: 10.1016/j.jaad.2019.11.015. Epub 2019 Nov 8.
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Drug survival of biologic agents for psoriatic patients in a real-world setting in Japan.
针对先前生物制剂暴露的白介素-17A 抑制剂反应:一项丹麦全国性研究。
Acta Derm Venereol. 2023 Nov 21;103:adv12616. doi: 10.2340/actadv.v103.12616.
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Treatment with Ixekizumab Following Secukinumab Failure in Patients with Psoriatic Arthritis: Real-Life Experience from a Resistant Population.司库奇尤单抗治疗失败后使用依奇珠单抗治疗银屑病关节炎患者:来自耐药人群的真实生活经验
Biologics. 2021 Nov 18;15:463-470. doi: 10.2147/BTT.S326792. eCollection 2021.
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