Paganini Claudia, Maffei Virginia, Vellucci Laura, Talamonti Marina, Petruzzellis Alessandra, Le Pera Lorenzo, Di Raimondo Cosimo, Bianchi Luca, Galluzzo Marco
Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
Dermatology Unit, Fondazione Policlinico Tor Vergata, 00133 Rome, Italy.
J Clin Med. 2024 Mar 24;13(7):1876. doi: 10.3390/jcm13071876.
Hand eczema (HE) is a prevalent chronic condition that exerts a substantial and enduring adverse effect on quality of life (QoL) and imposes an economic burden on society. Managing HE poses challenges due to the limited effectiveness and potential adverse effects associated with many currently available topical and systemic treatments. This article examines twenty-one patients affected by HE treated with dupilumab, a fully human monoclonal antibody targeting interleukin IL-4 and IL-13 signaling. This involves a retrospective descriptive statistical analysis. At week 6, HECSI-75 was achieved by 12 patients (57.9%). The proportion of patients meeting the HECSI-75 criteria steadily increased over the observation weeks, reaching 90% at week 16 and 100% at week 104. Furthermore, HECSI-90 and HECSI-100 were achieved by 75% and 60% of patients at week 16 and by 100% and 85% of patients at week 68, respectively. All patients who reached week 104 maintained complete disease remission according to HECSI 100. In all patients, dupilumab was shown to be an effective drug in achieving disease clearance, as indicated by all the parameters considered at each evaluation point (Week 6, Week 16, Week 32, Week 52, Week 68, Week 84, and Week 104), in comparison to the initial baseline.
手部湿疹(HE)是一种常见的慢性疾病,对生活质量(QoL)产生重大且持久的不利影响,并给社会带来经济负担。由于许多现有局部和全身治疗的有效性有限以及潜在的不良反应,手部湿疹的管理面临挑战。本文研究了21例接受度普利尤单抗治疗的手部湿疹患者,度普利尤单抗是一种靶向白细胞介素IL-4和IL-13信号传导的全人单克隆抗体。这涉及一项回顾性描述性统计分析。在第6周时,12例患者(57.9%)达到了手部湿疹临床严重程度指数(HECSI)-75。在观察周期间,达到HECSI-75标准的患者比例稳步增加,在第16周时达到90%,在第104周时达到100%。此外,分别有75%和60%的患者在第16周时达到HECSI-90和HECSI-100,在第68周时分别有100%和85%的患者达到。所有进入第104周的患者根据HECSI 100维持完全疾病缓解。在所有患者中,与初始基线相比,在每个评估点(第6周、第16周、第32周、第52周、第68周、第84周和第104周)考虑的所有参数均表明,度普利尤单抗是一种实现疾病清除的有效药物。