Department of Dermatology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
University of Toronto, Markham, ON, Canada.
Am J Clin Dermatol. 2023 May;24(3):469-483. doi: 10.1007/s40257-022-00754-4. Epub 2023 Feb 20.
Adults aged ≥ 60 years are often underrepresented in atopic dermatitis (AD) clinical trials; age-related comorbidities may impact treatment efficacy and safety.
The aim was to report dupilumab efficacy and safety in patients aged ≥ 60 years with moderate-to-severe AD.
Data were pooled from four randomized, placebo-controlled dupilumab trials of patients with moderate-to-severe AD (LIBERTY AD SOLO 1 and 2, LIBERTY AD CAFÉ, and LIBERTY AD CHRONOS) and stratified by age (< 60 [N = 2261] and ≥ 60 [N = 183] years). Patients received dupilumab 300 mg every week (qw) or every 2 weeks (q2w), or placebo with/without topical corticosteroids. Post hoc efficacy at week 16 was examined using broad categorical and continuous assessments of skin lesions, symptoms, biomarkers, and quality of life. Safety was also assessed.
In the ≥ 60-year-old group at week 16, a greater proportion of dupilumab-treated patients achieved an Investigator's Global Assessment score of 0/1 (q2w: 44.4%; qw: 39.7%) and 75% improvement in Eczema Area and Severity Index (63.0%; 61.6%) versus placebo (7.1% and 14.3%, respectively; P < 0.0001). Type 2 inflammation biomarkers (immunoglobulin E and thymus and activation-regulated chemokine) were also significantly reduced in dupilumab- versus placebo-treated patients (P < 0.01). Results were similar in the < 60-year-old group. The exposure-adjusted incidences of adverse events in dupilumab-treated patients were generally similar to those receiving placebo, with numerically fewer treatment-emergent adverse events in the dupilumab-treated ≥ 60-year-old group versus placebo.
There were fewer patients in the ≥ 60-year-old group; post hoc analyses.
Dupilumab improved AD signs and symptoms in patients aged ≥ 60 years; results were comparable to those in patients aged < 60 years. Safety was consistent with the known dupilumab safety profile.
ClinicalTrials.gov: NCT02277743, NCT02277769, NCT02755649, NCT02260986. Does dupilumab benefit adults aged 60 years and older with moderate-to-severe atopic dermatitis?(MP4 20,787 KB).
60 岁及以上成年人在特应性皮炎(AD)临床试验中常代表性不足;年龄相关合并症可能会影响治疗效果和安全性。
旨在报告达必妥在中重度 AD 患者中 60 岁及以上患者中的疗效和安全性。
数据来自四项达必妥治疗中重度 AD 的随机、安慰剂对照临床试验的汇总(LIBERTY AD SOLO1 和 2、LIBERTY AD CAFÉ 和 LIBERTY AD CHRONOS),并按年龄(<60 岁[N=2261]和≥60 岁[N=183]岁)进行分层。患者接受达必妥 300mg 每周一次(qw)或每两周一次(q2w),或联合/不联合局部皮质类固醇的安慰剂。使用皮肤损伤、症状、生物标志物和生活质量的广泛分类和连续评估,在第 16 周时进行事后疗效评估。还评估了安全性。
在第 16 周时≥60 岁的年龄组中,与安慰剂相比,更多的达必妥治疗患者达到研究者总体评估(IGA)评分 0/1(q2w:44.4%;qw:39.7%)和湿疹面积和严重程度指数(EASI)改善 75%(63.0%;61.6%;P<0.0001)。与安慰剂相比,达必妥治疗患者的 2 型炎症生物标志物(免疫球蛋白 E 和胸腺激活调节趋化因子)也显著降低(P<0.01)。<60 岁年龄组的结果相似。达必妥治疗患者的不良事件发生率与安慰剂相当,与安慰剂相比,达必妥治疗的≥60 岁年龄组中治疗出现的不良事件数量较少。
≥60 岁年龄组的患者较少;事后分析。
达必妥改善了≥60 岁年龄组患者的 AD 体征和症状;结果与<60 岁年龄组患者的结果相当。安全性与已知的达必妥安全性特征一致。
ClinicalTrials.gov:NCT02277743、NCT02277769、NCT02755649、NCT02260986。达必妥是否有益于 60 岁及以上中重度特应性皮炎患者?(MP4 20,787 KB)