Strizzolo Rémi, Seneschal Julien, Soria Angèle, Staumont-Sallé Delphine, Barbarot Sébastien, Viguier Manuelle, Jachiet Marie, Nosbaum Audrey, Clément Aude, Tauber Marie, Mallet Stéphanie, Du-Thanh Aurélie
Dermatology Department, University Hospital of Montpellier, Montpellier, France.
CHU de Bordeaux, National Reference Center for Rare Skin Diseases, CNRS UMR5164, ImmunoConCept, Univ. Bordeaux, Bordeaux, France.
World Allergy Organ J. 2024 Jul 4;17(7):100923. doi: 10.1016/j.waojou.2024.100923. eCollection 2024 Jul.
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.
在中度至重度特应性皮炎(AD)患者中,若对度普利尤单抗300mg/每2周的治疗反应不佳,很少有实际研究报道对维持度普利尤单抗治疗的替代方案的反应。为了评估和分析增加度普利尤单抗剂量或其与环孢素A(CsA)、甲氨蝶呤(MTX)或伊曲康唑(ITRA)联合使用的反应,对来自7家法国大学医院的所有成年AD患者进行了回顾性纳入,这些患者对度普利尤单抗300mg/每2周的治疗反应不佳,随后接受了增加剂量的度普利尤单抗(每7或10天300mg),或度普利尤单抗300mg/每2周与CsA、MTX或ITRA联合使用的治疗。收集了3个月后的反应情况以及流行病学、临床和治疗基线特征。总体而言,48例纳入患者中有68.75%的反应得到改善,其中完全缓解(CR)率为45.8%。没有一种策略被证明明显更好。初始无反应的患者从未实现进一步的CR,而初始部分反应的患者中有52.4%实现了进一步的CR(p = 0.025)。3例患者因消化不耐受和心动过速导致停用MTX和ITRA。增加度普利尤单抗剂量或与CsA、MTX或ITRA联合使用可能是替代且安全的选择,有待在进一步的药物经济学研究中进行评估。