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Comparative effectiveness of anti-IL5 and anti-IgE biologic classes in patients with severe asthma eligible for both

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dc.contributor Landspitali - The National University Hospital of Iceland
dc.contributor.author Pfeffer, Paul E
dc.contributor.author Ali, Nasloon
dc.contributor.author Murray, Ruth
dc.contributor.author Ulrik, Charlotte
dc.contributor.author Tran, Trung N
dc.contributor.author Maspero, Jorge
dc.contributor.author Peters, Matthew
dc.contributor.author Christoff, George C
dc.contributor.author Sadatsafavi, Mohsen
dc.contributor.author Torres-Duque, Carlos A
dc.contributor.author Altraja, Alan
dc.contributor.author Lehtimäki, Lauri
dc.contributor.author Papadopoulos, Nikolaos G
dc.contributor.author Salvi, Sundeep
dc.contributor.author Costello, Richard W
dc.contributor.author Cushen, Breda
dc.contributor.author Heffler, Enrico
dc.contributor.author Iwanaga, Takashi
dc.contributor.author Al-Ahmad, Mona
dc.contributor.author Larenas-Linnemann, Désirée
dc.contributor.author Kuna, Piotr
dc.contributor.author Fonseca, João A
dc.contributor.author Al-Lehebi, Riyad
dc.contributor.author Rhee, Chin Kook
dc.contributor.author Perez-de-Llano, Luis
dc.contributor.author Perng Steve, Diahn-Warng
dc.contributor.author Mahboub, Bassam
dc.contributor.author Wang, Eileen
dc.contributor.author Goh, Celine
dc.contributor.author Lyu, Juntao
dc.contributor.author Newell, Anthony
dc.contributor.author Alacqua, Marianna
dc.contributor.author Belevskiy, Andrey S
dc.contributor.author Bhutani, Mohit
dc.contributor.author Bjermer, Leif
dc.contributor.author Björnsdóttir, Unnur Steina
dc.contributor.author Bourdin, Arnaud
dc.contributor.author Bulow, Anna von
dc.contributor.author Busby, John
dc.contributor.author Canonica, Giorgio Walter
dc.contributor.author Cosio, Borja G
dc.contributor.author Dorscheid, Delbert R
dc.contributor.author Muñoz-Esquerre, Mariana
dc.contributor.author FitzGerald, J Mark
dc.contributor.author Gil, Esther Garcia
dc.contributor.author Gibson, Peter G
dc.contributor.author Heaney, Liam G
dc.contributor.author Hew, Mark
dc.contributor.author Hilberg, Ole
dc.contributor.author Hoyte, Flavia
dc.contributor.author Jackson, David J
dc.contributor.author Koh, Mariko Siyue
dc.contributor.author Ko, Hsin-Kuo Bruce
dc.contributor.author Lee, Jae Ha
dc.contributor.author Lehmann, Sverre
dc.contributor.author Chaves Loureiro, Cláudia
dc.contributor.author Lúðvíksdóttir, Dóra
dc.contributor.author Menzies-Gow, Andrew N
dc.contributor.author Mitchell, Patrick
dc.contributor.author Papaioannou, Andriana I
dc.contributor.author Popov, Todor A
dc.contributor.author Porsbjerg, Celeste M
dc.contributor.author Salameh, Laila
dc.contributor.author Sirena, Concetta
dc.contributor.author Taillé, Camille
dc.contributor.author Taube, Christian
dc.contributor.author Tohda, Yuji
dc.contributor.author Wechsler, Michael E
dc.contributor.author Price, David B
dc.date.accessioned 2023-11-04T01:05:32Z
dc.date.available 2023-11-04T01:05:32Z
dc.date.issued 2023-07
dc.identifier.citation Pfeffer , P E , Ali , N , Murray , R , Ulrik , C , Tran , T N , Maspero , J , Peters , M , Christoff , G C , Sadatsafavi , M , Torres-Duque , C A , Altraja , A , Lehtimäki , L , Papadopoulos , N G , Salvi , S , Costello , R W , Cushen , B , Heffler , E , Iwanaga , T , Al-Ahmad , M , Larenas-Linnemann , D , Kuna , P , Fonseca , J A , Al-Lehebi , R , Rhee , C K , Perez-de-Llano , L , Perng Steve , D-W , Mahboub , B , Wang , E , Goh , C , Lyu , J , Newell , A , Alacqua , M , Belevskiy , A S , Bhutani , M , Bjermer , L , Björnsdóttir , U S , Bourdin , A , Bulow , A V , Busby , J , Canonica , G W , Cosio , B G , Dorscheid , D R , Muñoz-Esquerre , M , FitzGerald , J M , Gil , E G , Gibson , P G , Heaney , L G , Hew , M , Hilberg , O , Hoyte , F , Jackson , D J , Koh , M S , Ko , H-K B , Lee , J H , Lehmann , S , Chaves Loureiro , C , Lúðvíksdóttir , D , Menzies-Gow , A N , Mitchell , P , Papaioannou , A I , Popov , T A , Porsbjerg , C M , Salameh , L , Sirena , C , Taillé , C , Taube , C , Tohda , Y , Wechsler , M E & Price , D B 2023 , ' Comparative effectiveness of anti-IL5 and anti-IgE biologic classes in patients with severe asthma eligible for both ' , Allergy , vol. 78 , no. 7 , pp. 1934-1948 . https://doi.org/10.1111/all.15711
dc.identifier.issn 0105-4538
dc.identifier.other 211014988
dc.identifier.other 9ad342b2-7a52-4eba-a424-fae088027c86
dc.identifier.other 36929509
dc.identifier.other 85151412409
dc.identifier.other unpaywall: 10.1111/all.15711
dc.identifier.uri https://hdl.handle.net/20.500.11815/4525
dc.description Publisher Copyright: © 2023 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.
dc.description.abstract BACKGROUND: Patients with severe asthma may present with characteristics representing overlapping phenotypes, making them eligible for more than one class of biologic. Our aim was to describe the profile of adult patients with severe asthma eligible for both anti-IgE and anti-IL5/5R and to compare the effectiveness of both classes of treatment in real life. METHODS: This was a prospective cohort study that included adult patients with severe asthma from 22 countries enrolled into the International Severe Asthma registry (ISAR) who were eligible for both anti-IgE and anti-IL5/5R. The effectiveness of anti-IgE and anti-IL5/5R was compared in a 1:1 matched cohort. Exacerbation rate was the primary effectiveness endpoint. Secondary endpoints included long-term-oral corticosteroid (LTOCS) use, asthma-related emergency room (ER) attendance, and hospital admissions. RESULTS: In the matched analysis (n = 350/group), the mean annualized exacerbation rate decreased by 47.1% in the anti-IL5/5R group and 38.7% in the anti-IgE group. Patients treated with anti-IL5/5R were less likely to experience a future exacerbation (adjusted IRR 0.76; 95% CI 0.64, 0.89; p < 0.001) and experienced a greater reduction in mean LTOCS dose than those treated with anti-IgE (37.44% vs. 20.55% reduction; p = 0.023). There was some evidence to suggest that patients treated with anti-IL5/5R experienced fewer asthma-related hospitalizations (IRR 0.64; 95% CI 0.38, 1.08), but not ER visits (IRR 0.94, 95% CI 0.61, 1.43). CONCLUSIONS: In real life, both anti-IgE and anti-IL5/5R improve asthma outcomes in patients eligible for both biologic classes; however, anti-IL5/5R was superior in terms of reducing asthma exacerbations and LTOCS use.
dc.format.extent 15
dc.format.extent 2480439
dc.format.extent 1934-1948
dc.language.iso en
dc.relation.ispartofseries Allergy; 78(7)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Lungnalæknisfræði
dc.subject Humans
dc.subject Adrenal Cortex Hormones/therapeutic use
dc.subject Anti-Asthmatic Agents
dc.subject Antibodies, Monoclonal, Humanized/therapeutic use
dc.subject Asthma/drug therapy
dc.subject Biological Products/therapeutic use
dc.subject Immunosuppressive Agents/therapeutic use
dc.subject Prospective Studies
dc.subject biologics
dc.subject oral corticosteroids
dc.subject exacerbation
dc.subject real life
dc.subject ISAR
dc.subject Immunology and Allergy
dc.subject Immunology
dc.title Comparative effectiveness of anti-IL5 and anti-IgE biologic classes in patients with severe asthma eligible for both
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1111/all.15711
dc.relation.url http://www.scopus.com/inward/record.url?scp=85151412409&partnerID=8YFLogxK
dc.contributor.department Other departments
dc.contributor.department Faculty of Medicine


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