{"title":"Upadacitinib和Dupilumab在治疗青少年特应性皮炎方面表现出优越的疗效:一项网络荟萃分析。","authors":"Zuotao Zhao, Chengyue Peng, Lijuan Liu, Yaqi Zheng, Yen Tan, Xiaoting Song, Peixin Zhang, Xiaojie Huang, Litao Zhang","doi":"10.1159/000543397","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>This systematic review and network meta-analysis aimed to compare and evaluate the efficacy and safety of five medications, dupilumab, tralokinumab, upadacitinib, baricitinib, and abrocitinib, for the treatment of adolescent atopic dermatitis (AD), in order to provide decision support to support clinical decision-making by developing more scientifically grounded and effective treatment strategies.</p><p><strong>Methods: </strong>A comprehensive search was conducted in PubMed, Embase, Web of Science (WoS), and the Cochrane database to collect randomized controlled trials (RCTs) and Phase 3 clinical trials up to April 13, 2024. Supplementary data were retrieved from trial registries, and researchers contacted study authors and pharmaceutical companies when necessary to obtain complete data. Inclusion criteria comprised treatment studies for moderate to severe AD in adolescents aged 12 and above, with outcome measures including efficacy and safety assessments. Data extraction and risk bias assessment were independently performed by two researchers, using Excel for data extraction and the netmeta package in R software for network meta-analysis. Sensitivity analysis and bias risk assessment were conducted to validate the robustness and credibility of the results. Our research protocol was registered in PROSPERO (CRD42023480597) and did not require approval from an Institutional Review Board or written informed consent.</p><p><strong>Results: </strong>In the primary efficacy outcome measures, upadacitinib 30 mg/day, upadacitinib 15 mg/day, and dupilumab 300 mg/2 weeks demonstrated excellent efficacy in EASI75 compared to placebo, significantly outperforming other medications and placebo. Dupilumab 300 mg/2 weeks, upadacitinib 30 mg/day, and upadacitinib 15 mg/day showed excellent treatment effects in IGA0/1. Among the outcome measures for improvement in itch severity rating PP-NRS4, dupilumab 300 mg/2 weeks and tralokinumab 300 mg/2 weeks showed the highest efficacy values. Compared to these medications, baricitinib 1 mg/day exhibited weaker performance across all three indicators, particularly in EASI75 and IGA0/1, with effects approaching no significant difference. Due to limited sample sizes, estimates for treatment-emergent adverse events, serious adverse events (SAEs), and drug-induced adverse events safety indicators were unstable, preventing strong conclusions on safety outcomes. There are significant differences in the incidence rates of adverse reactions such as nasopharyngitis, acne, and AD among various medications.</p><p><strong>Conclusion: </strong>Upadacitinib and dupilumab demonstrate strong efficacy and symptom improvement in the treatment of moderate to severe AD in adolescents, particularly in reducing the severity of skin lesions and itchiness. Therefore, these medications should be considered as primary treatment options for adolescents with AD. However, further studies with long-term follow-up and larger sample sizes are necessary to thoroughly investigate the safety profiles of these medications in adolescents. This underscores the importance of closely monitoring the side effects of different drugs during clinical treatment to tailor optimal therapeutic strategies based on individual patient needs.</p>","PeriodicalId":13652,"journal":{"name":"International Archives of Allergy and Immunology","volume":" ","pages":"1-11"},"PeriodicalIF":2.5000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Upadacitinib and Dupilumab Demonstrate Superior Efficacy in the Treatment of Adolescent Atopic Dermatitis: A Network Meta-Analysis.\",\"authors\":\"Zuotao Zhao, Chengyue Peng, Lijuan Liu, Yaqi Zheng, Yen Tan, Xiaoting Song, Peixin Zhang, Xiaojie Huang, Litao Zhang\",\"doi\":\"10.1159/000543397\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>This systematic review and network meta-analysis aimed to compare and evaluate the efficacy and safety of five medications, dupilumab, tralokinumab, upadacitinib, baricitinib, and abrocitinib, for the treatment of adolescent atopic dermatitis (AD), in order to provide decision support to support clinical decision-making by developing more scientifically grounded and effective treatment strategies.</p><p><strong>Methods: </strong>A comprehensive search was conducted in PubMed, Embase, Web of Science (WoS), and the Cochrane database to collect randomized controlled trials (RCTs) and Phase 3 clinical trials up to April 13, 2024. Supplementary data were retrieved from trial registries, and researchers contacted study authors and pharmaceutical companies when necessary to obtain complete data. Inclusion criteria comprised treatment studies for moderate to severe AD in adolescents aged 12 and above, with outcome measures including efficacy and safety assessments. Data extraction and risk bias assessment were independently performed by two researchers, using Excel for data extraction and the netmeta package in R software for network meta-analysis. Sensitivity analysis and bias risk assessment were conducted to validate the robustness and credibility of the results. Our research protocol was registered in PROSPERO (CRD42023480597) and did not require approval from an Institutional Review Board or written informed consent.</p><p><strong>Results: </strong>In the primary efficacy outcome measures, upadacitinib 30 mg/day, upadacitinib 15 mg/day, and dupilumab 300 mg/2 weeks demonstrated excellent efficacy in EASI75 compared to placebo, significantly outperforming other medications and placebo. Dupilumab 300 mg/2 weeks, upadacitinib 30 mg/day, and upadacitinib 15 mg/day showed excellent treatment effects in IGA0/1. Among the outcome measures for improvement in itch severity rating PP-NRS4, dupilumab 300 mg/2 weeks and tralokinumab 300 mg/2 weeks showed the highest efficacy values. Compared to these medications, baricitinib 1 mg/day exhibited weaker performance across all three indicators, particularly in EASI75 and IGA0/1, with effects approaching no significant difference. Due to limited sample sizes, estimates for treatment-emergent adverse events, serious adverse events (SAEs), and drug-induced adverse events safety indicators were unstable, preventing strong conclusions on safety outcomes. There are significant differences in the incidence rates of adverse reactions such as nasopharyngitis, acne, and AD among various medications.</p><p><strong>Conclusion: </strong>Upadacitinib and dupilumab demonstrate strong efficacy and symptom improvement in the treatment of moderate to severe AD in adolescents, particularly in reducing the severity of skin lesions and itchiness. Therefore, these medications should be considered as primary treatment options for adolescents with AD. However, further studies with long-term follow-up and larger sample sizes are necessary to thoroughly investigate the safety profiles of these medications in adolescents. This underscores the importance of closely monitoring the side effects of different drugs during clinical treatment to tailor optimal therapeutic strategies based on individual patient needs.</p>\",\"PeriodicalId\":13652,\"journal\":{\"name\":\"International Archives of Allergy and Immunology\",\"volume\":\" \",\"pages\":\"1-11\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-01-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Archives of Allergy and Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1159/000543397\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ALLERGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Archives of Allergy and Immunology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1159/000543397","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ALLERGY","Score":null,"Total":0}
Upadacitinib and Dupilumab Demonstrate Superior Efficacy in the Treatment of Adolescent Atopic Dermatitis: A Network Meta-Analysis.
Introduction: This systematic review and network meta-analysis aimed to compare and evaluate the efficacy and safety of five medications, dupilumab, tralokinumab, upadacitinib, baricitinib, and abrocitinib, for the treatment of adolescent atopic dermatitis (AD), in order to provide decision support to support clinical decision-making by developing more scientifically grounded and effective treatment strategies.
Methods: A comprehensive search was conducted in PubMed, Embase, Web of Science (WoS), and the Cochrane database to collect randomized controlled trials (RCTs) and Phase 3 clinical trials up to April 13, 2024. Supplementary data were retrieved from trial registries, and researchers contacted study authors and pharmaceutical companies when necessary to obtain complete data. Inclusion criteria comprised treatment studies for moderate to severe AD in adolescents aged 12 and above, with outcome measures including efficacy and safety assessments. Data extraction and risk bias assessment were independently performed by two researchers, using Excel for data extraction and the netmeta package in R software for network meta-analysis. Sensitivity analysis and bias risk assessment were conducted to validate the robustness and credibility of the results. Our research protocol was registered in PROSPERO (CRD42023480597) and did not require approval from an Institutional Review Board or written informed consent.
Results: In the primary efficacy outcome measures, upadacitinib 30 mg/day, upadacitinib 15 mg/day, and dupilumab 300 mg/2 weeks demonstrated excellent efficacy in EASI75 compared to placebo, significantly outperforming other medications and placebo. Dupilumab 300 mg/2 weeks, upadacitinib 30 mg/day, and upadacitinib 15 mg/day showed excellent treatment effects in IGA0/1. Among the outcome measures for improvement in itch severity rating PP-NRS4, dupilumab 300 mg/2 weeks and tralokinumab 300 mg/2 weeks showed the highest efficacy values. Compared to these medications, baricitinib 1 mg/day exhibited weaker performance across all three indicators, particularly in EASI75 and IGA0/1, with effects approaching no significant difference. Due to limited sample sizes, estimates for treatment-emergent adverse events, serious adverse events (SAEs), and drug-induced adverse events safety indicators were unstable, preventing strong conclusions on safety outcomes. There are significant differences in the incidence rates of adverse reactions such as nasopharyngitis, acne, and AD among various medications.
Conclusion: Upadacitinib and dupilumab demonstrate strong efficacy and symptom improvement in the treatment of moderate to severe AD in adolescents, particularly in reducing the severity of skin lesions and itchiness. Therefore, these medications should be considered as primary treatment options for adolescents with AD. However, further studies with long-term follow-up and larger sample sizes are necessary to thoroughly investigate the safety profiles of these medications in adolescents. This underscores the importance of closely monitoring the side effects of different drugs during clinical treatment to tailor optimal therapeutic strategies based on individual patient needs.
期刊介绍:
''International Archives of Allergy and Immunology'' provides a forum for basic and clinical research in modern molecular and cellular allergology and immunology. Appearing monthly, the journal publishes original work in the fields of allergy, immunopathology, immunogenetics, immunopharmacology, immunoendocrinology, tumor immunology, mucosal immunity, transplantation and immunology of infectious and connective tissue diseases.