Effect of omalizumab on outcomes in patients with aspirin-exacerbated respiratory disease

被引:30
|
作者
Jean, Tiffany [1 ,2 ]
Eng, Victoria [1 ]
Sheikh, Javed [1 ]
Kaplan, Michael S. [1 ]
Goldberg, Bruce [1 ]
Yang, Su Jau [3 ]
Samant, Shefali [1 ]
机构
[1] Kaiser Permanente Los Angeles Med Ctr, Dept Allergy & Immunol, Los Angeles, CA USA
[2] Univ Calif Irvine, Dept Clin Immunol & Allergy, Med Ctr, Irvine, CA USA
[3] Kaiser Permanente, Dept Res & Evaluat, Pasadena, CA USA
关键词
DESENSITIZATION;
D O I
10.2500/aap.2019.40.4241
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The current treatment for patients with aspirin-exacerbated respiratory disease (AERD) who have uncontrolled asthma or chronic rhinosinusitis is aspirin desensitization. For patients who are unable to undergo or do not benefit from aspirin desensitization, treatment with biologics is an option, although efficacy data for AERD is scarce. Objective: We reported a series of patients with AERD who were started on omalizumab and measured the outcomes to assess improvement. Methods: Adult patients with AERD who were initiated on omalizumab from January 2007 to January 2018 were included. We compared outcomes 6-12 months before initiating biologic therapy and during the last 6-12 months while they were on biologic therapy. Our study investigated the number of oral steroid courses, short-acting beta-agonists (SABA), antibiotics for sinusitis or pneumonia, emergency department visits, hospitalizations, pulmonary function tests, and changes in controller medications. Results: Twenty-nine patients were placed on omalizumab. Sixty-two percent demonstrated a reduction in the number of steroid courses (p = 0.0014) and number of SABA canisters used (p = 0.0005) during their last 12 months while on omalizumab. Eighty-six percent of the patients with AERD and on omalizumab demonstrated either a decrease in the number of steroid courses or number of SABA canisters used in the last year of the study. The patients with AERD and with concomitant immunoglobulin E (IgE) mediated respiratory disease showed a statistically significant reduction in the number of steroid courses and number of SABA canisters used while on omalizumab for 1 year (p = 0.002 and p = 0.005, respectively), whereas those without concomitant IgE-mediated respiratory disease did not have a substantial reduction in or SABA canisters used. Conclusion: Our case series reported that omalizumab could effectively be used as an adjunct treatment for AERD, but additional larger and longitudinal studies are needed to corroborate these findings.
引用
收藏
页码:316 / 320
页数:5
相关论文
共 50 条
  • [21] Aspirin desensitisation in a patient with aspirin-exacerbated urticaria and respiratory disease, achieved after treatment with omalizumab
    Calderon, O. M.
    Bobolea, I
    Guillen, D.
    Cabanas, R.
    Fiandor, A.
    Quirce, S.
    ALLERGY, 2013, 68 : 187 - 187
  • [22] Aspirin Desensitization Achieved After Omalizumab Treatment in a Patient With Aspirin-Exacerbated Urticaria and Respiratory Disease
    Guillen, D.
    Bobolea, I
    Calderon, O.
    Fiandor, A.
    Cabanas, R.
    Heredia, R.
    Quirce, S.
    JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, 2015, 25 (02) : 133 - 135
  • [23] Dysbiosis in aspirin-exacerbated respiratory disease
    Cook, Kevin A.
    Domissy, Alain
    Simon, Ronald A.
    White, Andrew A.
    Modena, Brian D.
    INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2021, 11 (07) : 1116 - 1120
  • [24] Omalizumab for Aspirin Hypersensitivity and Leukotriene Overproduction in Aspirin-exacerbated Respiratory Disease A Randomized Controlled Trial
    Hayashi, Hiroaki
    Fukutomi, Yuma
    Mitsui, Chihiro
    Kajiwara, Keiichi
    Watai, Kentaro
    Kamide, Yosuke
    Nakamura, Yuto
    Hamada, Yuto
    Tomita, Yasuhiro
    Sekiya, Kiyoshi
    Tsuburai, Takahiro
    Izuhara, Kenji
    Wakahara, Keiko
    Hashimoto, Naozumi
    Hasegawa, Yoshinori
    Taniguchi, Masami
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2020, 201 (12) : 1488 - 1498
  • [25] Aspirin-exacerbated Respiratory Disease (AERD)
    Klimek, Ludger
    ALLERGOLOGIE, 2014, 37 (01) : 2 - 3
  • [26] Aspirin-Exacerbated Respiratory Disease REPLY
    White, Andrew A.
    Stevenson, Donald D.
    NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (23): : 2281 - 2282
  • [27] Pathogenesis of aspirin-exacerbated respiratory disease
    Donald D. Stevenson
    Bruce L. Zuraw
    Clinical Reviews in Allergy & Immunology, 2003, 24 : 169 - 187
  • [28] Update on Aspirin-Exacerbated Respiratory Disease
    Woessner, Katharine M.
    CURRENT ALLERGY AND ASTHMA REPORTS, 2017, 17 (01)
  • [29] Aspirin-exacerbated respiratory disease: A review
    Dominas, Christine
    Gadkaree, Shekhar
    Maxfield, Alice Z.
    Gray, Stacey T.
    Bergmark, Regan W.
    LARYNGOSCOPE INVESTIGATIVE OTOLARYNGOLOGY, 2020, 5 (03): : 360 - 367
  • [30] Tolerability to Etoricoxib in Patients With Aspirin-Exacerbated Respiratory Disease
    Koschel, D.
    Weber, C. Ninck
    Hoeffken, G.
    JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, 2013, 23 (04) : 275 - 280