2024
DOI: 10.1089/derm.2022.0069
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Efficacy of Dupilumab in Children 6 Months to 11 Years Old With Atopic Dermatitis: A Retrospective Real-World Study in China

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Cited by 8 publications
(6 citation statements)
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“…The objective of vIGA 0-1 was reached by 95.2% at w24 and by 90.5% of patients at w40. The group of children younger than 6 years obtained faster responses than the older children [8]. These results were superior to those observed in our series (74% and 75% of vIGA 0-1 achievement at weeks 16 and 48, respectively).…”
Section: Discussioncontrasting
confidence: 83%
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“…The objective of vIGA 0-1 was reached by 95.2% at w24 and by 90.5% of patients at w40. The group of children younger than 6 years obtained faster responses than the older children [8]. These results were superior to those observed in our series (74% and 75% of vIGA 0-1 achievement at weeks 16 and 48, respectively).…”
Section: Discussioncontrasting
confidence: 83%
“…Although the results of both series are not directly comparable, it is likely that a higher severity of the patients included in our study (median EASI 25 vs. 21.3, previous use of oral immunosuppressants 94.7% vs. 3.5%) has contributed to these differences. Furthermore, dupilumab doses were higher in the study by Yang et al [8], since the 200 mg dose was administered every 2 weeks and not every 4 weeks as in our study. It would be interesting to continue exploring the best dosing of the drug, especially considering that higher doses have apparently not been associated with a higher frequency of adverse effects in these series [8].…”
Section: Discussionmentioning
confidence: 65%
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“…Notably, the SCORAD, NRS, CDLQI, and POEM were also signifcantly improved, which refects the dupiluamb beneft in aspects of patient-oriented disease burden, including daily pruritus, sleep disorder, school performance, and others. Diferent from other studies which showed no further improvement in EASI scores after W8 until W24 [11], and after 1 month until 6 months [12], respectively, our study revealed signifcant continued improvement in clinical scores from W10 to W16. One possible reason is that our study had higher baseline EASI scores (29.0 ± 16.2) compared to the other two studies (19.6 ± 13.9 and 19.23 ± 3.03), suggesting the necessity of completing the treatment until W16 for pediatric AD patients, at least for those with more severe eczematous lesions.…”
Section: Discussionsupporting
confidence: 74%