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 , 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","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 , 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\",\"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}
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.