Tofacitinib treatment for plaque psoriasis and psoriatic arthritis: A meta-analysis of randomised controlled trials.

IF 3.2 4区 医学 Q2 DERMATOLOGY
Tao Wang, Wei Wu, Xiaoqing Zhang, Bin Gan, Yanfang Zhou, Xiaoyan Cheng
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引用次数: 0

Abstract

Objectives Tofacitinib is used as an oral Janus-associated kinase (JAK) inhibitor acting on JAK1 and JAK3, in treating psoriatic disease. However, there is still no consensus on the optimal dosage and duration of tofacitinib. In this study, we aimed to evaluate the effects of tofacitinib in treating psoriatic disease. Methods and Materials A literature search was done utilising Cochrane library, Medline, EMBASE, Wiley Online library, Web of Science and BIOSIS Previews through December 18, 2022. We performed a meta-analysis of published original studies to assess the impact of tofacitinib in plaque psoriasis or psoriatic arthritis therapy based on seven randomised controlled trials (RCTs) involving 2,672 patients (receiving tofacitinib) and 853 controls (receiving placebo). Results Compared with placebo, the treatment of 5 mg twice-daily (BID) tofacitinib for 12 weeks is sufficient to significantly alleviate the main clinical manifestations of psoriasis [≥75% decrease in Psoriasis Area and Severity Index score (PASI 75): Risk ratio (RR)=4.38 (95% Confidence interval (CI) 2.51 to 7.64); ≥90% decrease in PASI score (PASI 90): RR=21.68 (95% CI 4.20 to 111.85); Physician's Global Assessment of 'clear' or 'almost clear' (PGA 0/1): RR=3.93 (95%CI 3.03 to 5.09)]. Interestingly, there was no significant difference in improvement in PGA 0/1 with 5 mg BID tofacitinib given for 16 weeks when compared with 5 mg BID tofacitinib for 12 weeks [RR=1.11 (95%CI 0.98 to 1.25)]. Additionally, the 5 mg BID tofacitinib for 16 weeks treatment schedule significantly increased the incidence of upper respiratory tract infection (URTI) [RR=1.89 (95%CI 1.06 to 3.38)] as compared to 5 mg BID tofacitinib for 12 weeks treatment schedule [RR=1.15 (95%CI 0.60 to 2.20)]. Conclusion The 5 mg BID tofacitinib for 12 weeks treatment significantly improved psoriasis without causing too many specific adverse events. This indicated that tofacitinib is an effective treatment plan for psoriatic disease by reasonably controlling dosage and dosing time.

托法替尼治疗斑块状银屑病和银屑病关节炎:随机对照试验的荟萃分析。
目的 托法替尼是一种口服Janus相关激酶(JAK)抑制剂,作用于JAK1和JAK3,用于治疗银屑病。然而,关于托法替尼的最佳剂量和疗程,目前仍未达成共识。本研究旨在评估托法替尼治疗银屑病的效果。方法和材料 我们利用 Cochrane 图书馆、Medline、EMBASE、Wiley Online 图书馆、Web of Science 和 BIOSIS Previews 进行了文献检索,检索时间截止到 2022 年 12 月 18 日。我们对已发表的原始研究进行了荟萃分析,以评估托法替尼对斑块型银屑病或银屑病关节炎治疗的影响,荟萃分析基于七项随机对照试验(RCT),涉及 2672 名患者(接受托法替尼治疗)和 853 名对照组患者(接受安慰剂治疗)。结果 与安慰剂相比,5 毫克、每日两次(BID)的托法替尼治疗 12 周足以显著缓解银屑病的主要临床表现[银屑病面积和严重程度指数评分(PASI 75)下降≥75%:风险比(RR)=4.38(95% 置信区间(CI)2.51 至 7.64);PASI 评分(PASI 90)下降≥90%:RR=21.68(95% 置信区间为 4.20 至 111.85);医生总体评估为 "无 "或 "基本无"(PGA 0/1):RR=3.93(95% 置信区间为 3.03 至 5.09)]。有趣的是,5 毫克托法替尼每日服用 16 周与 5 毫克托法替尼每日服用 12 周相比,PGA 0/1 的改善没有显著差异[RR=1.11(95%CI 0.98 至 1.25)]。此外,与5 mg BID tofacitinib治疗12周相比,5 mg BID tofacitinib治疗16周会显著增加上呼吸道感染(URTI)的发生率[RR=1.89(95%CI 1.06至3.38)][RR=1.15(95%CI 0.60至2.20)]。结论 5 mg BID tofacitinib 12 周治疗方案可显著改善银屑病,且不会引起过多特定不良事件。这表明,通过合理控制剂量和给药时间,托法替尼是治疗银屑病的有效方案。
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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来源期刊
CiteScore
2.10
自引率
10.30%
发文量
247
审稿时长
6-12 weeks
期刊介绍: The Indian Association of Dermatologists, Venereologists & Leprologists (IADVL) is the national association of Indian medical specialists who manage patients with skin disorders, sexually transmitted infections (STIs) or leprosy. The current member strength of the association is about 3800. The association works for the betterment of the specialty by holding academic meetings, printing a journal and publishing a textbook. The IADVL has several state branches, each with their own office bearers, which function independently within the constitution of the IADVL. Established in 1940, the Indian Journal of Dermatology, Venereology and Leprology (IJDVL, ISSN 0378-6323) is the official publication of the IADVL (Indian Association of Dermatologists, Venereologists and Leprologists).
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