Sheffield Dermatology Research, University of Sheffield, Sheffield, UK.
Sheffield Children's Hospital, Sheffield, UK.
Drug Des Devel Ther. 2024 Feb 3;18:277-289. doi: 10.2147/DDDT.S426947. eCollection 2024.
Atopic dermatitis (AD) is the most common inflammatory skin disease in children. Children with severe AD have a multidimensional disease burden characterized by skin lesions, itching, frequent infections, sleep deprivation, and a high rate of comorbidities. These impact the mental health and overall quality of life of not only the children but also of their parents and caregivers. There are few effective available treatment options for young children with severe AD that are suitable for long-term use. Due to their adverse effects, practice guidelines consider systemic agents inappropriate for this age group, although they are still used off-label in extreme cases. The biologic dupilumab has recently been approved for children aged 6-11 years with severe (EU) and moderate-to-severe (USA) AD, offering hope to this population of patients with a high unmet clinical need. The purpose of this review is to describe the unmet needs of AD patients aged 6-11 years prior to dupilumab approval and to summarize existing clinical data supporting dupilumab's safety and efficacy in these children.
特应性皮炎(AD)是儿童中最常见的炎症性皮肤病。患有严重 AD 的儿童疾病负担多维度,其特征为皮肤损伤、瘙痒、频繁感染、睡眠剥夺以及合并症发生率高。这些不仅会影响儿童本身,还会影响其父母和照顾者的心理健康和整体生活质量。对于患有严重 AD 的幼儿,适合长期使用的有效治疗方案很少。由于其不良反应,实践指南认为全身性药物不适合该年龄组,尽管在极端情况下仍会被超适应证使用。生物制剂度普利尤单抗最近已获批用于 6-11 岁患有严重(EU)和中重度至重度(USA)AD 的儿童,为这一具有高度未满足临床需求的患者群体带来了希望。本文旨在描述度普利尤单抗获批前 6-11 岁 AD 患者的未满足需求,并总结现有临床数据支持度普利尤单抗在这些儿童中的安全性和疗效。