From the Department of Dermatology, The George Washington University School of Medicine and Health Sciences, Washington, DC.
Oregon Health & Science University, Portland.
Dermatitis. 2021 Oct 1;32(1S):S81-S91. doi: 10.1097/DER.0000000000000698.
Pain is a frequent symptom of atopic dermatitis (AD).
The aims of the study were to evaluate the effects of dupilumab on pain/discomfort in AD and to determine whether pain correlates with other outcomes.
This was a post hoc analysis of 5 randomized, placebo-controlled clinical trials in which adults with chronic AD received placebo or dupilumab 300 mg every 2 weeks or once weekly with and without topical corticosteroids. Proportions of patients with no pain/discomfort on this dimension of the 5-dimension EuroQoL (EQ-5D) at week 16 (all trials) and week 52 (CHRONOS) were compared between placebo and dupilumab. Correlations were evaluated between pain/discomfort and signs and symptoms of AD.
Among 2632 evaluated patients, 72.9% to 83.1% reported at least moderate pain/discomfort at baseline. Higher proportions treated with dupilumab reported no pain/discomfort at week 16 relative to placebo; risk differences ranged from 22.3% (95% confidence interval = 11.5%-33.1%) to 42.2% (95% confidence interval = 26.6%-57.8%, all P ≤ 0.0001), with similar effects observed at week 52. Correlations at baseline of pain/discomfort with signs and symptoms of AD were low to moderate.
Pain/discomfort, present in a substantial proportion of patients with moderate-to-severe AD, was significantly reduced by dupilumab treatment. Given the low-to-moderate correlations with other AD symptoms at baseline, pain likely represents a distinct AD symptom.Trial Registration: ClinicalTrials.gov identifiers NCT01859988, NCT02277743, NCT02277769, NCT02260986, and NCT02755649.
疼痛是特应性皮炎(AD)的常见症状。
本研究旨在评估度普利尤单抗对 AD 患者疼痛/不适的影响,并确定疼痛是否与其他结果相关。
这是对 5 项随机、安慰剂对照临床试验的事后分析,其中慢性 AD 成人患者接受安慰剂或度普利尤单抗 300mg,每 2 周或每周一次,同时使用或不使用局部皮质类固醇。在所有试验中,比较了在第 16 周(所有试验)和第 52 周(CHRONOS),5 维度欧洲五维健康量表(EQ-5D)这一维度无疼痛/不适的患者比例,与安慰剂相比,度普利尤单抗的比例更高。还评估了疼痛/不适与 AD 体征和症状之间的相关性。
在 2632 例评估患者中,72.9%至 83.1%的患者在基线时报告至少有中度疼痛/不适。与安慰剂相比,接受度普利尤单抗治疗的患者报告在第 16 周无疼痛/不适的比例更高;风险差异范围为 22.3%(95%置信区间=11.5%-33.1%)至 42.2%(95%置信区间=26.6%-57.8%,所有 P≤0.0001),在第 52 周也观察到类似的效果。基线时疼痛/不适与 AD 体征和症状的相关性为低至中度。
在患有中重度 AD 的患者中,疼痛/不适的比例相当大,度普利尤单抗治疗显著减轻了疼痛。鉴于在基线时与其他 AD 症状的相关性较低,疼痛可能代表 AD 的一个独特症状。
ClinicalTrials.gov 标识符 NCT01859988、NCT02277743、NCT02277769、NCT02260986 和 NCT02755649。