Suppr超能文献

银屑病患者生物制剂的剂量递减:范围综述。

Dose Tapering of Biologics in Patients with Psoriasis: A Scoping Review.

机构信息

Radboud University Medical Center, Radboud Institute for Health Sciences, Mailbox 9101, 6500 HB, Nijmegen, The Netherlands.

Department of Dermatology, Radboud University Medical Center, Nijmegen, The Netherlands.

出版信息

Drugs. 2021 Feb;81(3):349-366. doi: 10.1007/s40265-020-01448-z.

Abstract

INTRODUCTION

Biologics serve as a cornerstone in psoriasis treatment, with low disease activity or sometimes even clinical remission as a realistic treatment outcome. So far, it is unclear whether biologics should be tapered when this target is achieved. Dose tapering could offer potential benefits by decreasing side effects, the burden of repetitive injections and costs of biological therapy. However, clinical guidelines on dose tapering of biologicals in psoriasis patients are lacking. This scoping review was conducted to provide an overview of the current literature on dose tapering and offer guidance for clinicians in daily clinical practice.

METHODS

Dose tapering is defined as the administration of a lower dose per administration, or the prolongation of the regular dose interval, after initial treatment according to the standard dosing. Four electronic databases (PubMed, EMBASE, Cochrane, and Web of Science) were systematically searched for literature on tapering of biologics in adult patients with psoriasis from 1 January 2000.

RESULTS

We included 19 original articles on biologic tapering in psoriasis patients: four randomized controlled trials and 15 observational studies. Tapering eligibility criteria, tapering strategies, tapering outcomes, and recapture of response after relapse were assessed. Furthermore, the available evidence on possible predictors for successful tapering, and the effect of tapering on safety, quality of life and costs is summarized. The definition of low disease activity as a measure for tapering eligibility varied widely. Beside tapering criteria, tapering strategies were also heterogeneous. Of note, quality-of-life measurements were barely integrated in the evaluation of tapering outcomes. Literature on regaining response after relapse due to tapering was limited, but restored remission has been described. The included studies did not proclaim a significant effect of tapering on the occurrence of (severe) adverse events. Even though cost savings have been reported, no proper cost-effectiveness analysis has been conducted yet.

CONCLUSION

Biologic tapering seems to be effective and safe in psoriasis patients with stable low disease activity or clinical remission. Available data on biologic dose tapering in patients with psoriasis are promising, but more research is warranted to fill the current gaps in knowledge.

摘要

简介

生物制剂是治疗银屑病的基石,实现低疾病活动度甚至临床缓解是现实的治疗目标。到目前为止,尚不清楚在达到这一目标时是否应该减少生物制剂的剂量。减少剂量可以通过降低副作用、减少重复注射的负担和生物治疗的成本来提供潜在的益处。然而,目前缺乏关于银屑病患者生物制剂剂量减少的临床指南。本范围综述旨在提供生物制剂剂量减少的当前文献概述,并为临床医生的日常临床实践提供指导。

方法

剂量减少被定义为根据标准剂量进行初始治疗后,每次给药减少给药剂量或延长常规剂量间隔。从 2000 年 1 月 1 日起,我们系统性地在四个电子数据库(PubMed、EMBASE、Cochrane 和 Web of Science)中搜索了关于成人银屑病患者生物制剂减量的文献。

结果

我们纳入了 19 篇关于银屑病患者生物制剂减量的原始文章:四项随机对照试验和 15 项观察性研究。评估了减量的合格标准、减量策略、减量结果以及复发后的应答恢复情况。此外,还总结了关于成功减量的可能预测因素以及减量对安全性、生活质量和成本的影响的现有证据。将低疾病活动度定义为减量合格标准的指标差异很大。除了减量标准外,减量策略也存在差异。值得注意的是,生活质量测量在减量结果的评估中几乎没有被纳入。由于减量而导致复发后恢复应答的文献有限,但已描述了恢复缓解。纳入的研究并未宣称减量对(严重)不良事件的发生有显著影响。尽管有报道称可以节省成本,但尚未进行适当的成本效益分析。

结论

在疾病活动度稳定或临床缓解的银屑病患者中,生物制剂减量似乎是有效且安全的。关于银屑病患者生物制剂剂量减少的现有数据很有希望,但需要进一步研究来填补目前知识空白。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验