4.5 Article

Dupilumab Significantly Modulates Pain and Discomfort in Patients With Atopic Dermatitis: A Post Hoc Analysis of 5 Randomized Clinical Trials

Journal

DERMATITIS
Volume 32, Issue 1S, Pages S81-S91

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/DER.0000000000000698

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Funding

  1. Sanofi (Bridgewater, NJ)
  2. Regeneron Pharmaceuticals, Inc (Tarrytown, NY)

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This study analyzed the effects of dupilumab on pain/discomfort in atopic dermatitis (AD) patients and found that dupilumab treatment significantly reduced pain/discomfort compared to placebo. Correlations between pain/discomfort and other symptoms of AD were low to moderate.
Background: Pain is a frequent symptom of atopic dermatitis (AD). Objectives: 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. Methods: 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. Results: 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. Conclusions: 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.

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