Alqahtani Saad, Khalil Samia, Bakhamees Basel H, Almutairi Layan M, Alyahya Mariyah A, Alghuyaythat Waleed Khalid Z, Alabdulqader Fatimah K, Aldossary Dana, Asiri Shuruq Talea B, Alsulami Talal A, Hussain Abdulrahman A, Alaamer Mohammed A
Family Medicine, King Salman Armed Forces Hospital, Tabuk, SAU.
Medicine and Surgery, Ibn Sina National College for Medical Studies, Jeddah, SAU.
Cureus. 2024 Sep 25;16(9):e70196. doi: 10.7759/cureus.70196. eCollection 2024 Sep.
Psoriasis is a clinically heterogeneous, lifelong skin condition. Novel medications such as Janus kinase (JAK) inhibitors have emerged as a promising class of agents that modulate the immune response. Tofacitinib could reduce skin lesions and boost patient-reported clinical outcomes, but its immunosuppressive effects might also increase patients' risk of infections and other adverse effects. To assess the safety outcomes of using Tofacitinib in comparison to placebo in terms of the incidence of serious infections, herpes zoster infection (HZ), upper respiratory tract infections (URTI), nasopharyngitis, and serious adverse events (SAE), this systematic review and meta-analysis followed the Cochrane Handbook for Systematic Reviews and Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. The search strategy involved five databases. Two authors independently screened and selected studies. Only randomized controlled trials (RCTs) were eligible for inclusion. Data on baseline patient characteristics and outcomes such as serious infections, HZ infections, nasopharyngitis, and URTIs were extracted. The risk of bias was assessed using the revised version of the Cochrane risk of bias (ROB2) tool, and meta-analysis was conducted using Cochrane's Revman web. The OR was employed to estimate outcomes. A probability value of less than 0.05 was considered statistically significant. The search strategy initially identified 998 studies; of these, six RCTs were included with a total of 2516 participants having moderate-to-severe psoriasis and treated with either Tofacitinib or placebo. The meta-analysis results revealed increases in the risks of HZ, URTIs, serious infections, nasopharyngitis, and SAE, but no significant difference was found between the intervention and placebo groups. The risk of bias was assessed using the ROB2 tool, revealing low bias across most domains, with some concerns in certain studies related to deviations from intended interventions and missing outcome data. In conclusion, while Tofacitinib is effective against moderate-to-severe psoriasis with non-significant risks, there are some safety concerns regarding the measured outcomes. Future research is needed concerning the assessment of safety outcomes with long-term use of Tofacitinib among larger populations.
银屑病是一种临床上具有异质性的、终身性的皮肤疾病。新型药物如Janus激酶(JAK)抑制剂已成为一类有前景的调节免疫反应的药物。托法替布可以减少皮肤病变并改善患者报告的临床结局,但其免疫抑制作用也可能增加患者感染及其他不良反应的风险。为了评估与安慰剂相比,使用托法替布在严重感染、带状疱疹感染(HZ)、上呼吸道感染(URTI)、鼻咽炎和严重不良事件(SAE)发生率方面的安全性结局,本系统评价和荟萃分析遵循了Cochrane系统评价手册以及系统评价和荟萃分析的首选报告项目(PRISMA)指南。检索策略涉及五个数据库。两位作者独立筛选和选择研究。仅随机对照试验(RCT)符合纳入标准。提取了关于患者基线特征以及严重感染、HZ感染、鼻咽炎和URTI等结局的数据。使用Cochrane偏倚风险(ROB2)工具的修订版评估偏倚风险,并使用Cochrane的Revman网络进行荟萃分析。采用比值比(OR)来估计结局。概率值小于0.05被认为具有统计学意义。检索策略最初识别出998项研究;其中,纳入了6项RCT,共有2516名中度至重度银屑病患者接受托法替布或安慰剂治疗。荟萃分析结果显示,HZ、URTI、严重感染、鼻咽炎和SAE的风险增加,但干预组和安慰剂组之间未发现显著差异。使用ROB2工具评估偏倚风险,结果显示大多数领域的偏倚较低,某些研究在与预期干预措施的偏差和缺失结局数据方面存在一些问题。总之,虽然托法替布对中度至重度银屑病有效且风险不显著,但在所测量的结局方面存在一些安全问题。需要对更大规模人群长期使用托法替布的安全性结局评估进行进一步研究。