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

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  • Paul E. Pfeffer
  • Nasloon Ali
  • Ruth Murray
  • Trung N. Tran
  • Jorge Maspero
  • Matthew Peters
  • George C. Christoff
  • Mohsen Sadatsafavi
  • Carlos A. Torres-Duque
  • Alan Altraja
  • Lauri Lehtimäki
  • Nikolaos G Papadopoulos
  • Sundeep Salvi
  • Richard W. Costello
  • Breda Cushen
  • Enrico Heffler
  • Takashi Iwanaga
  • Mona Al-Ahmad
  • Désirée Larenas-Linnemann
  • Piotr Kuna
  • João A. Fonseca
  • Riyad Al-Lehebi
  • Chin Kook Rhee
  • Luis Perez-de-Llano
  • Diahn Warng Perng Steve
  • Bassam Mahboub
  • Eileen Wang
  • Celine Goh
  • Juntao Lyu
  • Anthony Newell
  • Marianna Alacqua
  • Andrey S. Belevskiy
  • Mohit Bhutani
  • Leif Bjermer
  • Unnur Bjornsdottir
  • Arnaud Bourdin
  • Anna von Bulow
  • John Busby
  • Giorgio Walter Canonica
  • Borja G. Cosio
  • Delbert R. Dorscheid
  • Mariana Muñoz-Esquerre
  • J. Mark FitzGerald
  • Esther Garcia Gil
  • Peter G. Gibson
  • Liam G. Heaney
  • Mark Hew
  • Ole Hilberg
  • Flavia Hoyte
  • David J. Jackson
  • Mariko Siyue Koh
  • Hsin Kuo Bruce Ko
  • Jae Ha Lee
  • Sverre Lehmann
  • Cláudia Chaves Loureiro
  • Dóra Lúðvíksdóttir
  • Andrew N. Menzies-Gow
  • Patrick Mitchell
  • Andriana I. Papaioannou
  • Todor A. Popov
  • Laila Salameh
  • Concetta Sirena
  • Camille Taillé
  • Christian Taube
  • Yuji Tohda
  • Michael E. Wechsler
  • David B. Price
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.
OriginalsprogEngelsk
TidsskriftAllergy: European Journal of Allergy and Clinical Immunology
Vol/bind78
Udgave nummer7
Sider (fra-til)1934-1948
Antal sider15
ISSN0105-4538
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
This study was conducted by the Observational and Pragmatic Research Institute (OPRI) Pte Ltd and was partially funded by Optimum Patient Care Global and AstraZeneca Ltd. No funding was received by the Observational & Pragmatic Research Institute Pte Ltd (OPRI) for its contribution.

Publisher Copyright:
© 2023 The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

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