TY - JOUR
T1 - Comparative effectiveness of dupilumab and omalizumab on asthma exacerbations and systemic corticosteroid prescriptions
T2 - Real-world US ADVANTAGE study
AU - Bleecker, Eugene
AU - Blaiss, Michael
AU - Jacob-Nara, Juby
AU - Huynh, Lynn
AU - Duh, Mei Sheng
AU - Guo, Tracy
AU - Ye, Mingchen
AU - Stanford, Richard H.
AU - Wang, Zhixiao
AU - Soler, Xavier
AU - Nag, Arpita
AU - Nair, Radhika
AU - Borsos, Kinga
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/12
Y1 - 2024/12
N2 - Background: In the United States, dupilumab is approved for moderate-to-severe eosinophilic or oral corticosteroid–dependent asthma, and omalizumab is approved for managing moderate-to-severe allergic asthma uncontrolled by inhaled corticosteroids. However, limited comparative effectiveness data exist for these biologics due to differing patient characteristics and treatment histories. Objective: This study assessed the real-world effectiveness of dupilumab and omalizumab for asthma in patients in the United States. Methods: In this retrospective observational study, TriNetX Dataworks electronic medical record data were used to identify patients with asthma age ≥12 years who initiated (index) dupilumab or omalizumab between November 2018 and September 2020 and who had at least 12 months of pre- and post-index clinical information. Inverse probability of treatment weighting was applied to balance potential confounding in treatment groups. Asthma exacerbation rates and systemic corticosteroid (SCS) prescriptions were compared using a doubly robust negative binomial regression model, adjusting for baseline exacerbation/SCS rates and patient characteristics with ≥10% standardized differences after inverse probability of treatment weighting. Results: All inclusion and exclusion criteria were met by 2138 dupilumab patients and 1313 omalizumab patients. After weighting, the majority of baseline characteristics were balanced (standard difference <10%) between the 2 groups. Dupilumab was associated with a 44% lower asthma exacerbation rate (P <. 0001) versus omalizumab. Additionally, dupilumab treatment significantly (P <. 05) reduced SCS prescriptions by 28% during the follow-up period compared with omalizumab treatment. Conclusions: The US ADVANTAGE real-world study demonstrated a significant reduction in severe asthma exacerbations and SCS prescriptions for patients prescribed dupilumab compared with patients prescribed omalizumab during 12 months of follow-up.
AB - Background: In the United States, dupilumab is approved for moderate-to-severe eosinophilic or oral corticosteroid–dependent asthma, and omalizumab is approved for managing moderate-to-severe allergic asthma uncontrolled by inhaled corticosteroids. However, limited comparative effectiveness data exist for these biologics due to differing patient characteristics and treatment histories. Objective: This study assessed the real-world effectiveness of dupilumab and omalizumab for asthma in patients in the United States. Methods: In this retrospective observational study, TriNetX Dataworks electronic medical record data were used to identify patients with asthma age ≥12 years who initiated (index) dupilumab or omalizumab between November 2018 and September 2020 and who had at least 12 months of pre- and post-index clinical information. Inverse probability of treatment weighting was applied to balance potential confounding in treatment groups. Asthma exacerbation rates and systemic corticosteroid (SCS) prescriptions were compared using a doubly robust negative binomial regression model, adjusting for baseline exacerbation/SCS rates and patient characteristics with ≥10% standardized differences after inverse probability of treatment weighting. Results: All inclusion and exclusion criteria were met by 2138 dupilumab patients and 1313 omalizumab patients. After weighting, the majority of baseline characteristics were balanced (standard difference <10%) between the 2 groups. Dupilumab was associated with a 44% lower asthma exacerbation rate (P <. 0001) versus omalizumab. Additionally, dupilumab treatment significantly (P <. 05) reduced SCS prescriptions by 28% during the follow-up period compared with omalizumab treatment. Conclusions: The US ADVANTAGE real-world study demonstrated a significant reduction in severe asthma exacerbations and SCS prescriptions for patients prescribed dupilumab compared with patients prescribed omalizumab during 12 months of follow-up.
KW - allergic asthma
KW - asthma exacerbations
KW - comparative effectiveness
KW - Dupilumab
KW - eosinophilic asthma
KW - inhaled corticosteroids
KW - moderate-to-severe asthma
KW - omalizumab
KW - real-world study
KW - systemic corticosteroids
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U2 - 10.1016/j.jaci.2024.07.029
DO - 10.1016/j.jaci.2024.07.029
M3 - Article
C2 - 39186985
AN - SCOPUS:85204791128
SN - 0091-6749
VL - 154
SP - 1500
EP - 1510
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 6
ER -