Omalizumab in patients with NSAIDs-exacerbated respiratory disease.


Journal

Rhinology
ISSN: 0300-0729
Titre abrégé: Rhinology
Pays: Netherlands
ID NLM: 0347242

Informations de publication

Date de publication:
01 Jun 2020
Historique:
pubmed: 23 2 2020
medline: 28 10 2020
entrez: 21 2 2020
Statut: ppublish

Résumé

The association of acetylsalicylic acid (ASA) intolerance, chronic rhinosinusitis with nasal polyps (CRSwNP), asthma, or chronic urticaria is known as NSAID-exacerbated respiratory disease (N-ERD). N-ERD patients often suffer from recurrent nasal polyps, severe asthma or also from urticaria. The aim of the present study was to retrospectively analyze the clinical efficacy of anti-IgE antibody treatment with omalizumab in patients with confirmed N-ERD. In the open trial with patients receiving verum patients with CRSwNP, confirmed N-ERD by oral or nasal ASA challenges, asthma or chronic urticaria were included in the study. Rhinological and pulmonary parameters were evaluated before and after 3, 6 and 9 months of therapy by rhinological questionnaires (CRS VAS-scores and RSOM-31), nasal polyp (NP)-, ACT-scores and FEV1 values. Urticaria activity was monitored clinically. N-ERD patients with aspirin desensitization were included as control group (follow-up 9 months). In the omalizumab group 16 patients were included (10 female, 6 male, mean age 51 yrs). CRS symptoms, RSOM-31- and NP-score decreased significantly following omalizumab therapy compared to baseline. The ACT-score (MV 16.5 to 20.6) and FEV1values (MV 80 % to 89 %) improved significantly. No urticaria symptoms were reported after 3 months. Oral prednisolone therapy was required in one case and a repeated nasal sinus surgery in an additional case due to progression of NP. In the control group (8 female, 8 male, mean age 45 yrs) the NP-score was unchanged. Omalizumab is an effective therapy option in N-ERD patients in a 9 month study period.

Sections du résumé

BACKGROUND BACKGROUND
The association of acetylsalicylic acid (ASA) intolerance, chronic rhinosinusitis with nasal polyps (CRSwNP), asthma, or chronic urticaria is known as NSAID-exacerbated respiratory disease (N-ERD). N-ERD patients often suffer from recurrent nasal polyps, severe asthma or also from urticaria. The aim of the present study was to retrospectively analyze the clinical efficacy of anti-IgE antibody treatment with omalizumab in patients with confirmed N-ERD.
METHODS METHODS
In the open trial with patients receiving verum patients with CRSwNP, confirmed N-ERD by oral or nasal ASA challenges, asthma or chronic urticaria were included in the study. Rhinological and pulmonary parameters were evaluated before and after 3, 6 and 9 months of therapy by rhinological questionnaires (CRS VAS-scores and RSOM-31), nasal polyp (NP)-, ACT-scores and FEV1 values. Urticaria activity was monitored clinically. N-ERD patients with aspirin desensitization were included as control group (follow-up 9 months).
RESULTS RESULTS
In the omalizumab group 16 patients were included (10 female, 6 male, mean age 51 yrs). CRS symptoms, RSOM-31- and NP-score decreased significantly following omalizumab therapy compared to baseline. The ACT-score (MV 16.5 to 20.6) and FEV1values (MV 80 % to 89 %) improved significantly. No urticaria symptoms were reported after 3 months. Oral prednisolone therapy was required in one case and a repeated nasal sinus surgery in an additional case due to progression of NP. In the control group (8 female, 8 male, mean age 45 yrs) the NP-score was unchanged.
CONCLUSIONS CONCLUSIONS
Omalizumab is an effective therapy option in N-ERD patients in a 9 month study period.

Identifiants

pubmed: 32077449
pii: 2354
doi: 10.4193/Rhin19.318
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Omalizumab 2P471X1Z11

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

226-232

Auteurs

U Forster-Ruhrmann (U)

Department of Oto-Rhino-Laryngology, Campus Virchow-Klinikum, Charite - Universitatsmedizin Berlin, Berlin, Germany; Department of Oto-Rhino-Laryngology, Campus Mitte, Charite - Universitatsmedizin Berlin, Berlin, Germany.

D Stergioudi (D)

Department of Oto-Rhino-Laryngology, Campus Virchow-Klinikum, Charite - Universitatsmedizin Berlin, Berlin, Germany; Department of Oto-Rhino-Laryngology, Campus Mitte, Charite - Universitatsmedizin Berlin, Berlin, Germany.

G Pierchalla (G)

Department of Oto-Rhino-Laryngology, Campus Virchow-Klinikum, Charite - Universitatsmedizin Berlin, Berlin, Germany; Department of Oto-Rhino-Laryngology, Campus Mitte, Charite - Universitatsmedizin Berlin, Berlin, Germany.

J W Fluhr (JW)

Clinic for Dermatology, Venerology and Allergy, Charite - Universitatsmedizin Berlin, Berlin, Germany.

K-C Bergmann (KC)

Clinic for Dermatology, Venerology and Allergy, Charite - Universitatsmedizin Berlin, Berlin, Germany.

H Olze (H)

Department of Oto-Rhino-Laryngology, Campus Virchow-Klinikum, Charite - Universitatsmedizin Berlin, Berlin, Germany; Department of Oto-Rhino-Laryngology, Campus Mitte, Charite - Universitatsmedizin Berlin, Berlin, Germany.

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