特应性皮炎患者对标示内使用的杜必鲁单抗反应不佳的实际处理方法

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-01 DOI:10.1016/j.waojou.2024.100923
Rémi Strizzolo MD , Julien Seneschal MD, PhD , Angèle Soria MD, PhD , Delphine Staumont-Sallé MD, PhD , Sébastien Barbarot MD, PhD , Manuelle Viguier MD, PhD , Marie Jachiet MD , Audrey Nosbaum MD, PhD , Aude Clément MD , Marie Tauber MD, PhD , Stéphanie Mallet MD , Aurélie Du-Thanh MD, PhD , the French Atopic Dermatitis Network from the GREAT Research group
{"title":"特应性皮炎患者对标示内使用的杜必鲁单抗反应不佳的实际处理方法","authors":"Rémi Strizzolo MD ,&nbsp;Julien Seneschal MD, PhD ,&nbsp;Angèle Soria MD, PhD ,&nbsp;Delphine Staumont-Sallé MD, PhD ,&nbsp;Sébastien Barbarot MD, PhD ,&nbsp;Manuelle Viguier MD, PhD ,&nbsp;Marie Jachiet MD ,&nbsp;Audrey Nosbaum MD, PhD ,&nbsp;Aude Clément MD ,&nbsp;Marie Tauber MD, PhD ,&nbsp;Stéphanie Mallet MD ,&nbsp;Aurélie Du-Thanh MD, PhD ,&nbsp;the French Atopic Dermatitis Network from the GREAT Research group","doi":"10.1016/j.waojou.2024.100923","DOIUrl":null,"url":null,"abstract":"<div><p>In patients with moderate to severe atopic dermatitis (AD) showing an inadequate response to dupilumab 300mg/2weeks, few real-life studies reported the response to alternative regimen maintaining dupilumab.</p><p>To assess and analyze the response to an increased dose of dupilumab or its combination with cyclosporin A (CsA), methotrexate (MTX), or itraconazole (ITRA), all adult AD patients from 7 French University Hospitals were retrospectively included if they achieved an inadequate response to dupilumab 300mg/2weeks and were subsequently treated with an increased dose of dupilumab (300mg every 7 or 10 days), or a combination of dupilumab 300mg/2weeks with CsA, MTX or ITRA. The response after 3 months, along with epidemiological, clinical, and therapeutic baseline characteristics, were collected.</p><p>Overall, 68.75% of the 48 included patients achieved an improved response, including 45.8% of complete response (CR). No strategy proved significantly better. Patients showing an initial no response never achieved a further CR versus 52.4% of patients with an initial partial response (p = 0.025). Digestive intolerance and tachycardia led to MTX and ITRA discontinuation in 3 patients.</p><p>Increasing the dose of dupilumab or combining it with CsA, MTX, or ITRA could be alternative and safe options, to be evaluated in further medico-economic studies.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1939455124000541/pdfft?md5=44a112f9cdbbbd643537b08cb92c26d0&pid=1-s2.0-S1939455124000541-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Real-life management of atopic dermatitis patients with an inadequate response to on-label use of dupilumab\",\"authors\":\"Rémi Strizzolo MD ,&nbsp;Julien Seneschal MD, PhD ,&nbsp;Angèle Soria MD, PhD ,&nbsp;Delphine Staumont-Sallé MD, PhD ,&nbsp;Sébastien Barbarot MD, PhD ,&nbsp;Manuelle Viguier MD, PhD ,&nbsp;Marie Jachiet MD ,&nbsp;Audrey Nosbaum MD, PhD ,&nbsp;Aude Clément MD ,&nbsp;Marie Tauber MD, PhD ,&nbsp;Stéphanie Mallet MD ,&nbsp;Aurélie Du-Thanh MD, PhD ,&nbsp;the French Atopic Dermatitis Network from the GREAT Research group\",\"doi\":\"10.1016/j.waojou.2024.100923\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In patients with moderate to severe atopic dermatitis (AD) showing an inadequate response to dupilumab 300mg/2weeks, few real-life studies reported the response to alternative regimen maintaining dupilumab.</p><p>To assess and analyze the response to an increased dose of dupilumab or its combination with cyclosporin A (CsA), methotrexate (MTX), or itraconazole (ITRA), all adult AD patients from 7 French University Hospitals were retrospectively included if they achieved an inadequate response to dupilumab 300mg/2weeks and were subsequently treated with an increased dose of dupilumab (300mg every 7 or 10 days), or a combination of dupilumab 300mg/2weeks with CsA, MTX or ITRA. The response after 3 months, along with epidemiological, clinical, and therapeutic baseline characteristics, were collected.</p><p>Overall, 68.75% of the 48 included patients achieved an improved response, including 45.8% of complete response (CR). No strategy proved significantly better. Patients showing an initial no response never achieved a further CR versus 52.4% of patients with an initial partial response (p = 0.025). Digestive intolerance and tachycardia led to MTX and ITRA discontinuation in 3 patients.</p><p>Increasing the dose of dupilumab or combining it with CsA, MTX, or ITRA could be alternative and safe options, to be evaluated in further medico-economic studies.</p></div>\",\"PeriodicalId\":3,\"journal\":{\"name\":\"ACS Applied Electronic Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1939455124000541/pdfft?md5=44a112f9cdbbbd643537b08cb92c26d0&pid=1-s2.0-S1939455124000541-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Electronic Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1939455124000541\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1939455124000541","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0

摘要

中度至重度特应性皮炎(AD)患者对杜比鲁单抗 300 毫克/两周的反应不充分,很少有实际研究报告维持杜比鲁单抗的替代方案的反应。为了评估和分析对增加剂量的杜比卢单抗或其与环孢素 A (CsA)、甲氨蝶呤 (MTX) 或伊曲康唑 (ITRA) 联用的反应、回顾性纳入法国 7 家大学医院的所有成人 AD 患者,如果他们对杜比单抗 300 毫克/两周的治疗反应不充分,随后接受了增加剂量的杜比单抗(300 毫克,每 7 天或 10 天一次)或杜比单抗 300 毫克/两周与环孢素 A、MTX 或伊曲康唑的联合治疗。研究人员收集了3个月后的反应以及流行病学、临床和治疗基线特征。总体而言,48名纳入研究的患者中有68.75%获得了改善反应,包括45.8%的完全反应(CR)。事实证明,没有任何一种策略能明显提高疗效。最初无应答的患者从未进一步获得 CR,而最初部分应答的患者中有 52.4%获得了 CR(p = 0.025)。增加dupilumab的剂量或将其与CsA、MTX或ITRA联用可能是安全的替代选择,有待进一步的医学经济学研究进行评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Real-life management of atopic dermatitis patients with an inadequate response to on-label use of dupilumab

In patients with moderate to severe atopic dermatitis (AD) showing an inadequate response to dupilumab 300mg/2weeks, few real-life studies reported the response to alternative regimen maintaining dupilumab.

To assess and analyze the response to an increased dose of dupilumab or its combination with cyclosporin A (CsA), methotrexate (MTX), or itraconazole (ITRA), all adult AD patients from 7 French University Hospitals were retrospectively included if they achieved an inadequate response to dupilumab 300mg/2weeks and were subsequently treated with an increased dose of dupilumab (300mg every 7 or 10 days), or a combination of dupilumab 300mg/2weeks with CsA, MTX or ITRA. The response after 3 months, along with epidemiological, clinical, and therapeutic baseline characteristics, were collected.

Overall, 68.75% of the 48 included patients achieved an improved response, including 45.8% of complete response (CR). No strategy proved significantly better. Patients showing an initial no response never achieved a further CR versus 52.4% of patients with an initial partial response (p = 0.025). Digestive intolerance and tachycardia led to MTX and ITRA discontinuation in 3 patients.

Increasing the dose of dupilumab or combining it with CsA, MTX, or ITRA could be alternative and safe options, to be evaluated in further medico-economic studies.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
期刊最新文献
Hyperbaric oxygen treatment promotes tendon-bone interface healing in a rabbit model of rotator cuff tears. Oxygen-ozone therapy for myocardial ischemic stroke and cardiovascular disorders. Comparative study on the anti-inflammatory and protective effects of different oxygen therapy regimens on lipopolysaccharide-induced acute lung injury in mice. Heme oxygenase/carbon monoxide system and development of the heart. Hyperbaric oxygen for moderate-to-severe traumatic brain injury: outcomes 5-8 years after injury.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1