Real-life management of atopic dermatitis patients with an inadequate response to on-label use of dupilumab

IF 3.9 2区 医学 Q2 ALLERGY World Allergy Organization Journal 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
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Abstract

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.

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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
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。
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来源期刊
World Allergy Organization Journal
World Allergy Organization Journal Immunology and Microbiology-Immunology
CiteScore
9.10
自引率
5.90%
发文量
91
审稿时长
9 weeks
期刊介绍: The official pubication of the World Allergy Organization, the World Allergy Organization Journal (WAOjournal) publishes original mechanistic, translational, and clinical research on the topics of allergy, asthma, anaphylaxis, and clincial immunology, as well as reviews, guidelines, and position papers that contribute to the improvement of patient care. WAOjournal publishes research on the growth of allergy prevalence within the scope of single countries, country comparisons, and practical global issues and regulations, or threats to the allergy specialty. The Journal invites the submissions of all authors interested in publishing on current global problems in allergy, asthma, anaphylaxis, and immunology. Of particular interest are the immunological consequences of climate change and the subsequent systematic transformations in food habits and their consequences for the allergy/immunology discipline.
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