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Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study

BACKGROUND: Atopic dermatitis (AD) is a common skin disease, but treatment of this disease has been challenging. Dupilumab is a new biological agent for AD that has been proven to be safe and effective in clinical trials. Although dupilumab was approved for listing in China in June 2020, real-world...

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Autores principales: Zhou, Bingjing, Peng, Cong, Li, Liqiao, Liu, Runqiu, Zhu, Lei, Chen, Xiang, Li, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984471/
https://www.ncbi.nlm.nih.gov/pubmed/35402441
http://dx.doi.org/10.3389/fmed.2022.838030
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author Zhou, Bingjing
Peng, Cong
Li, Liqiao
Liu, Runqiu
Zhu, Lei
Chen, Xiang
Li, Jie
author_facet Zhou, Bingjing
Peng, Cong
Li, Liqiao
Liu, Runqiu
Zhu, Lei
Chen, Xiang
Li, Jie
author_sort Zhou, Bingjing
collection PubMed
description BACKGROUND: Atopic dermatitis (AD) is a common skin disease, but treatment of this disease has been challenging. Dupilumab is a new biological agent for AD that has been proven to be safe and effective in clinical trials. Although dupilumab was approved for listing in China in June 2020, real-world data about the application of dupilumab in China are lacking. This study aimed to collect and analyze real-world data on dupilumab among Chinese AD patients. METHODS: Demographic and clinical data for 116 AD patients receiving dupilumab treatment were reviewed. The Eczema Area and Severity Index (EASI), SCORing Atopic Dermatitis (SCORAD), Numerical Rating Scale (NRS), Patient Oriented Eczema Measure (POEM), and Dermatology Quality of Life Index (DLQI) of patients were evaluated every 2 weeks from baseline to 16 weeks of treatment. Any adverse events during treatment were recorded. RESULTS: Among the 116 patients in this study, baseline levels of IgE, eosinophils, and LDH were elevated in 62.79% (n = 86), 45.30% (n = 86), and 54.20% of patients (n = 48), respectively. The SCORAD index and POEM, DLQI, and NRS scores were significantly improved in all patients at 2 weeks (p < 0.0001), 4 weeks (p < 0.01), and 16 weeks (p < 0.001). EASI scores also improved significantly in all patients at 2 weeks (p < 0.01), 4 weeks (> 0.05), and 16 weeks (p < 0.01). However, 11 patients (9.48%) had no response. IgE and LDH levels (p > 0.05), Eosinophil counts (p < 0.01) in blood increased temporarily in the first 4 weeks and then decreased and stabilized during dupilumab treatment. Conjunctivitis was the most common adverse event (2.59%) among the patients. We found that the curative efficacy of dupilumab at 4th weeks was related to the patient’s age and course of disease. Nevertheless, there is no relationship between levels of eosinophils, IgE, LDH and the therapeutic efficacy of dupilumab. CONCLUSION: The real-world data in China showed that dupilumab can effectively treat AD and is well tolerated with a low incidence of adverse events.
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spelling pubmed-89844712022-04-07 Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study Zhou, Bingjing Peng, Cong Li, Liqiao Liu, Runqiu Zhu, Lei Chen, Xiang Li, Jie Front Med (Lausanne) Medicine BACKGROUND: Atopic dermatitis (AD) is a common skin disease, but treatment of this disease has been challenging. Dupilumab is a new biological agent for AD that has been proven to be safe and effective in clinical trials. Although dupilumab was approved for listing in China in June 2020, real-world data about the application of dupilumab in China are lacking. This study aimed to collect and analyze real-world data on dupilumab among Chinese AD patients. METHODS: Demographic and clinical data for 116 AD patients receiving dupilumab treatment were reviewed. The Eczema Area and Severity Index (EASI), SCORing Atopic Dermatitis (SCORAD), Numerical Rating Scale (NRS), Patient Oriented Eczema Measure (POEM), and Dermatology Quality of Life Index (DLQI) of patients were evaluated every 2 weeks from baseline to 16 weeks of treatment. Any adverse events during treatment were recorded. RESULTS: Among the 116 patients in this study, baseline levels of IgE, eosinophils, and LDH were elevated in 62.79% (n = 86), 45.30% (n = 86), and 54.20% of patients (n = 48), respectively. The SCORAD index and POEM, DLQI, and NRS scores were significantly improved in all patients at 2 weeks (p < 0.0001), 4 weeks (p < 0.01), and 16 weeks (p < 0.001). EASI scores also improved significantly in all patients at 2 weeks (p < 0.01), 4 weeks (> 0.05), and 16 weeks (p < 0.01). However, 11 patients (9.48%) had no response. IgE and LDH levels (p > 0.05), Eosinophil counts (p < 0.01) in blood increased temporarily in the first 4 weeks and then decreased and stabilized during dupilumab treatment. Conjunctivitis was the most common adverse event (2.59%) among the patients. We found that the curative efficacy of dupilumab at 4th weeks was related to the patient’s age and course of disease. Nevertheless, there is no relationship between levels of eosinophils, IgE, LDH and the therapeutic efficacy of dupilumab. CONCLUSION: The real-world data in China showed that dupilumab can effectively treat AD and is well tolerated with a low incidence of adverse events. Frontiers Media S.A. 2022-03-23 /pmc/articles/PMC8984471/ /pubmed/35402441 http://dx.doi.org/10.3389/fmed.2022.838030 Text en Copyright © 2022 Zhou, Peng, Li, Liu, Zhu, Chen and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Zhou, Bingjing
Peng, Cong
Li, Liqiao
Liu, Runqiu
Zhu, Lei
Chen, Xiang
Li, Jie
Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study
title Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study
title_full Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study
title_fullStr Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study
title_full_unstemmed Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study
title_short Efficacy and Safety of Dupilumab in Chinese Patients With Atopic Dermatitis: A Real-World Study
title_sort efficacy and safety of dupilumab in chinese patients with atopic dermatitis: a real-world study
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984471/
https://www.ncbi.nlm.nih.gov/pubmed/35402441
http://dx.doi.org/10.3389/fmed.2022.838030
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