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Adults who were taking dupilumab for their atopic dermatitis also experienced significant improvements in their mild asthma, primarily in the first 16 weeks, according to a study published in Clinical and Translational Allergy.
Led by Lotte S. Spekhorst, MD, department of dermatology and allergology and National Expertise Center for Atopic Dermatitis at University Medical Center Utrecht, the Netherlands, the study involved 304 adults with mild asthma receiving dupilumab (Dupixent; Sanofi Genzyme, Regeneron) for AD.
Mean Asthma Control Questionnaire (ACQ)-5 scores significantly improved from 1.32 (95% CI, 1.2-1.45; n = 236) at baseline by –0.24 (95% CI, –0.38 to -0.1; n = 173) at week 16 and –0.26 (95% CI, –0.43 to –0.09; n = 110) at week 52.
Also, mean FEV1 significantly improved from 2.96 L (95% CI, 2.79-3.13; n = 104) at baseline by 0.1 L (95% CI, 0.03-0.16; n = 81) at week 16 and 0.12 L (95% CI, 0.05-0.19; n = 64) at week 52.
Median fractional exhaled nitric oxide significantly decreased from 22.43 ppb (95% CI, 16.37-33.53; n = 22) at baseline to 13.13 ppb (95% CI, 10.49-16.45; n = 17) at week 16, increasing to 15.24 ppb (95% CI, 12.38-18.76; n = 21) at week 52.
The proportion of patients with an ACQ-5 score of less than 0.5 increased from 20.8% at baseline to 28.2% at week 52. Similarly, the proportion of patients with an FEV1 percentage of 80% or higher increased from 58.7% to 68.8%.
However, the researchers did not find any profound effect of type 2 (T2)-indicator blood eosinophilia at the start of treatment with dupilumab indicating its effectiveness on FEV1, suggesting that the effect of dupilumab on patients with mild asthma may depend less on T2-indicator blood eosinophilia.
Considering these findings, the researchers wrote that patients who receive dupilumab for their AD experience additional benefits if they also have asthma.