Aspirin desensitization and biologics in aspirin-exacerbated respiratory disease: Efficacy, tolerability, and patient experience.


Journal

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
ISSN: 1534-4436
Titre abrégé: Ann Allergy Asthma Immunol
Pays: United States
ID NLM: 9503580

Informations de publication

Date de publication:
05 2022
Historique:
received: 17 12 2021
revised: 20 01 2022
accepted: 31 01 2022
pubmed: 9 2 2022
medline: 4 5 2022
entrez: 8 2 2022
Statut: ppublish

Résumé

Patterns of medication use and efficacy in aspirin-exacerbated respiratory disease (AERD) have not been well characterized, especially since the advent of respiratory biologics. Aspirin therapy after desensitization (ATAD) is efficacious for upper and lower respiratory symptoms for patients with AERD, though aspirin-related adverse effects can limit therapy. The optimal coordination of ATAD and respiratory biologics for the treatment of AERD remains unclear. We aimed to characterize patterns of medication use and treatment experience with biologics and ATAD in AERD. We surveyed 98 patients with AERD recruited from the Brigham and Women's Hospital AERD registry. Patients completed an online questionnaire describing their medication history and treatment experience. A total of 52 (53.0%) patients reported a history of use of one or more respiratory biologics (omalizumab, mepolizumab, reslizumab, benralizumab, or dupilumab), and 84 (85.7%) reported undergoing aspirin desensitization. There were 24 patients (24.4%) who reported concurrent use of a biologic and ATAD. Compared with those taking ATAD alone, patients taking a biologic and ATAD concurrently were less likely to report that aspirin was effective for their AERD symptoms (odds ratio, 0.161 [95% confidence interval, 0.03-0.76]; P =.02). Whereas patients reported varying efficacy with biologics, dupilumab had the highest odds of patients reporting it worked "very well" (odds ratio, 17.58 [95% confidence interval, 5.68-54.35]; P < .001). Biologics are emerging as a treatment option for AERD and are generally well tolerated. Biologic efficacy in AERD is variable by agent, though most patients taking dupilumab found it to be effective. Patients on a biologic in conjunction with ATAD may represent a more severe subset of AERD for which ATAD alone is insufficient.

Sections du résumé

BACKGROUND
Patterns of medication use and efficacy in aspirin-exacerbated respiratory disease (AERD) have not been well characterized, especially since the advent of respiratory biologics. Aspirin therapy after desensitization (ATAD) is efficacious for upper and lower respiratory symptoms for patients with AERD, though aspirin-related adverse effects can limit therapy. The optimal coordination of ATAD and respiratory biologics for the treatment of AERD remains unclear.
OBJECTIVE
We aimed to characterize patterns of medication use and treatment experience with biologics and ATAD in AERD.
METHODS
We surveyed 98 patients with AERD recruited from the Brigham and Women's Hospital AERD registry. Patients completed an online questionnaire describing their medication history and treatment experience.
RESULTS
A total of 52 (53.0%) patients reported a history of use of one or more respiratory biologics (omalizumab, mepolizumab, reslizumab, benralizumab, or dupilumab), and 84 (85.7%) reported undergoing aspirin desensitization. There were 24 patients (24.4%) who reported concurrent use of a biologic and ATAD. Compared with those taking ATAD alone, patients taking a biologic and ATAD concurrently were less likely to report that aspirin was effective for their AERD symptoms (odds ratio, 0.161 [95% confidence interval, 0.03-0.76]; P =.02). Whereas patients reported varying efficacy with biologics, dupilumab had the highest odds of patients reporting it worked "very well" (odds ratio, 17.58 [95% confidence interval, 5.68-54.35]; P < .001).
CONCLUSION
Biologics are emerging as a treatment option for AERD and are generally well tolerated. Biologic efficacy in AERD is variable by agent, though most patients taking dupilumab found it to be effective. Patients on a biologic in conjunction with ATAD may represent a more severe subset of AERD for which ATAD alone is insufficient.

Identifiants

pubmed: 35131410
pii: S1081-1206(22)00090-4
doi: 10.1016/j.anai.2022.01.043
pmc: PMC9058196
mid: NIHMS1777804
pii:
doi:

Substances chimiques

Biological Products 0
Aspirin R16CO5Y76E

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

575-582

Subventions

Organisme : NIAID NIH HHS
ID : K23 AI139352
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL128241
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007306
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI095219
Pays : United States

Informations de copyright

Copyright © 2022 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Références

J Allergy Clin Immunol. 2020 Sep;146(3):595-605
pubmed: 32524991
Clin Immunol. 2015 Oct;160(2):349-57
pubmed: 26083948
J Allergy Clin Immunol Pract. 2022 Feb;10(2):478-484.e3
pubmed: 34597850
N Engl J Med. 2018 Jun 28;378(26):2486-2496
pubmed: 29782217
J Allergy Clin Immunol. 2021 Aug;148(2):574-584
pubmed: 34144111
N Engl J Med. 2014 Sep 25;371(13):1198-207
pubmed: 25199059
J Allergy Clin Immunol Pract. 2021 Jul;9(7):2910-2912.e1
pubmed: 33631410
Am J Respir Crit Care Med. 2020 Jun 15;201(12):1488-1498
pubmed: 32142372
J Allergy Clin Immunol. 2022 Apr;149(4):1309-1317.e12
pubmed: 34599979
J Allergy Clin Immunol Pract. 2015 Sep-Oct;3(5):711-8
pubmed: 25858054
Allergy. 2013;68(5):659-65
pubmed: 23464577
J Allergy Clin Immunol Pract. 2021 Apr;9(4):1604-1611
pubmed: 33307278
Rhinology. 2020 Aug 1;58(4):333-340
pubmed: 32219224
J Allergy Clin Immunol Pract. 2019 Sep - Oct;7(7):2462-2465.e1
pubmed: 30954643
Lancet. 2019 Nov 2;394(10209):1638-1650
pubmed: 31543428
Int Forum Allergy Rhinol. 2019 Dec;9(12):1409-1419
pubmed: 31518069
Lancet Respir Med. 2021 Oct;9(10):1141-1153
pubmed: 33872587
Iran J Pharm Res. 2017 Fall;16(4):1639-1647
pubmed: 29552073
J Allergy Clin Immunol Pract. 2018 May - Jun;6(3):1045-1047
pubmed: 29501519
Chest. 2004 Apr;125(4):1378-86
pubmed: 15078749
J Allergy Clin Immunol. 2021 Aug;148(2):348-350
pubmed: 34174296
Am J Rhinol Allergy. 2018 Jul;32(4):280-286
pubmed: 29682983
J Allergy Clin Immunol. 2021 Mar;147(3):827-844
pubmed: 33307116
J Allergy Clin Immunol. 1984 Apr;73(4):500-7
pubmed: 6368649

Auteurs

Jyotsna Mullur (J)

Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.

Camille M Steger (CM)

Center for Clinical Investigation, Brigham and Women's Hospital, Boston, Massachusetts.

Deborah Gakpo (D)

Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Jillian C Bensko (JC)

Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Rie Maurer (R)

Center for Clinical Investigation, Brigham and Women's Hospital, Boston, Massachusetts.

Tanya M Laidlaw (TM)

Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts.

Kathleen M Buchheit (KM)

Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts. Electronic address: kbuchheit@bwh.harvard.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH