Randomized evidence breadth and comparative maturity of systemic targeted therapies for prurigo nodularis: a time-aligned systematic review and network meta-analysis.

IF 3.9
Yanchen Liu, Haoran Hu, Linfeng Li
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Abstract

Objectives: Randomized evidence for systemic targeted therapies in prurigo nodularis (PN) has expanded, but cross-trial differences limit valid comparison. We mapped randomized evidence and assessed comparative effects using exact Week-16 ≥ 4-point itch numerical rating scale response (NRS4).

Methods: MEDLINE, Embase, CENTRAL, and Web of Science were searched through 14 August 2026. Studies with extractable randomized arm-level Week-16 NRS4 data were synthesized using a fixed-effect contrast-based network meta-analysis. Risk of bias was assessed with RoB 2 and confidence with CINeMA.

Results: Twenty-four randomized studies were represented by 117 reports, but only seven cohorts (1,435 participants; 19 arms; 10 active nodes) contributed to the aligned network. Dupilumab (OR 4.04, 95% CI 2.42-6.75; low confidence) and global phase III nemolizumab (OR 5.81, 95% CI 3.81-8.86; low confidence) were effective versus placebo. The indirect nemolizumab-versus-dupilumab comparison was imprecise (OR 1.44, 95% CI 0.74-2.79; low confidence).

Conclusions: Indirect evidence did not establish superiority of either biologic. The randomized evidence bases substantially exceeded the quantitatively comparable network, reflecting incomplete results availability and cross-trial differences.

Registration: PROSPERO CRD420261401106.

结节性痒疹的系统性靶向治疗的随机证据广度和比较成熟度:一项时间对齐的系统评价和网络荟萃分析。
目的:系统性靶向治疗结节性痒疹(PN)的随机证据已经扩大,但交叉试验的差异限制了有效的比较。我们绘制了随机证据,并使用精确的第16周≥4点瘙痒数值评定量表反应(NRS4)评估了比较效果。方法:检索至2026年8月14日的MEDLINE、Embase、CENTRAL和Web of Science。采用基于固定效应对比的网络meta分析,对可提取的随机臂级第16周NRS4数据进行综合研究。偏倚风险用RoB 2评估,置信度用CINeMA评估。结果:117份报告代表了24项随机研究,但只有7个队列(1435名参与者,19个组,10个活动节点)对对齐网络做出了贡献。Dupilumab (OR 4.04, 95% CI 2.42-6.75;低置信度)和全球III期nemolizumab (OR 5.81, 95% CI 3.81-8.86;低置信度)与安慰剂相比有效。奈莫单抗与杜匹单抗的间接比较是不精确的(OR 1.44, 95% CI 0.74-2.79;低置信度)。结论:间接证据不能确定两种生物制剂的优越性。随机证据基础大大超过了数量上可比较的网络,反映了不完整的结果可用性和交叉试验差异。注册号:PROSPERO CRD420261401106。
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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