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现实世界中中重度斑块状银屑病生物治疗的剂量调整:一项系统评价

Dose Adjustment of Biologic Treatments for Moderate-to-Severe Plaque Psoriasis in the Real World: A Systematic Review.

作者信息

Gambardella Alessio, Licata Gaetano, Sohrt Anne

机构信息

Università degli Studi della Campania "Luigi Vanvitelli", Caserta, Italy.

LEO Pharma A/S, Ballerup, Denmark.

出版信息

Dermatol Ther (Heidelb). 2021 Aug;11(4):1141-1156. doi: 10.1007/s13555-021-00559-z. Epub 2021 Jun 3.

Abstract

INTRODUCTION

Dose escalation and reduction of biologic treatments are frequent in clinical practice. The aim of this systematic review is to summarise evidence on dose adjustment of biologic treatments for moderate-to-severe plaque psoriasis in the real-world.

METHODS

A systematic review of real-world evidence on dose adjustment of biologics for plaque psoriasis was performed. Searches were conducted in BIOSIS Previews, Embase, International Pharmaceutical Abstracts, MEDLINE, and SciSearch in March 2020. Real-world studies that reported biologic dose adjustment for moderate-to-severe plaque psoriasis were included.

RESULTS

The search identified 162 papers, and 20 studies with 30,912 patients were included from 2014 to 2020. More studies reported on dose escalation than dose reduction. For adalimumab, 3-54% of patients had dose reduction while 0-37% had dose escalation. For infliximab, only two studies reported a dose reduction, with rates of 22-29%, while dose escalation rates varied from 14 to 67%. Dose reduction rates of 5-49% were reported for etanercept while 0-55% of patients had doses escalated. For ustekinumab, dose escalation and reduction rates ranged from 3 to 37% and 7 to 42%, respectively. Two studies reported on dose adjustment for secukinumab; in one 52% of patients initiated on 150 mg instead of the recommended 300 mg, while another reported no dose increase.

CONCLUSIONS

Dose adjustment of biologics for psoriasis is common, with escalation more frequently reported than reduction. Dose escalation may have economic and safety consequences, while dose reduction may impact efficacy. These aspects are important to consider when making decisions on treatment dosing.

摘要

引言

在临床实践中,生物治疗的剂量递增和递减很常见。本系统评价的目的是总结现实世界中中重度斑块状银屑病生物治疗剂量调整的证据。

方法

对斑块状银屑病生物制剂剂量调整的现实世界证据进行系统评价。2020年3月在BIOSIS Previews、Embase、国际药学文摘、MEDLINE和SciSearch中进行检索。纳入报告中重度斑块状银屑病生物制剂剂量调整的现实世界研究。

结果

检索到162篇论文,纳入了2014年至2020年的20项研究,共30912例患者。报告剂量递增的研究比剂量递减的更多。对于阿达木单抗,3%-54%的患者有剂量减少,而0%-37%的患者有剂量增加。对于英夫利昔单抗,只有两项研究报告了剂量减少,比例为22%-29%,而剂量增加率在14%至67%之间。报告依那西普的剂量减少率为5%-49%,而0%-55%的患者有剂量增加。对于乌司奴单抗,剂量增加率和减少率分别为3%至37%和7%至42%。两项研究报告了司库奇尤单抗的剂量调整;一项研究中,52%的患者起始剂量为150mg而非推荐的300mg,而另一项研究报告无剂量增加。

结论

银屑病生物制剂的剂量调整很常见,报告剂量递增的情况比递减更频繁。剂量递增可能会产生经济和安全后果,而剂量减少可能会影响疗效。在做出治疗剂量决策时,这些方面很重要,需要考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a8c/8322248/9159d77af877/13555_2021_559_Fig1_HTML.jpg

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