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Omalizumab is effective in nasal polyposis with or without asthma, a real-life study
BACKGROUND: Chronic rhinosinusitis with nasal polyposis (CRSwNP) can be recalcitrant in some patients despite medical therapies and surgery and has higher morbidity. Omalizumab is a new treatment option for patients with CRSwNP. The aim of this study is to evaluate the efficacy and safety of omalizu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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World Allergy Organization
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9382317/ https://www.ncbi.nlm.nih.gov/pubmed/36017064 http://dx.doi.org/10.1016/j.waojou.2022.100670 |
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author | Tat, Tuğba Songül |
author_facet | Tat, Tuğba Songül |
author_sort | Tat, Tuğba Songül |
collection | PubMed |
description | BACKGROUND: Chronic rhinosinusitis with nasal polyposis (CRSwNP) can be recalcitrant in some patients despite medical therapies and surgery and has higher morbidity. Omalizumab is a new treatment option for patients with CRSwNP. The aim of this study is to evaluate the efficacy and safety of omalizumab (anti-IgE antibody) in patients with CRSwNP. METHODS: The efficiency and adverse effects of omalizumab were evaluated based on the data extracted from medical records of patients with CRSwNP. Patients were evaluated monthly for efficacy and adverse reactions. Treatment efficacy was evaluated by visual analog scale (VAS) for rhinorrhea, postnasal drip, sneeze, smell, and nasal stuffiness complaints, sinonasal outcome test-22 (SNOT-22), and nose obstruction symptom evaluation (NOSE) score. RESULTS: 17 patients with CRSwNP formed our cohort. The mean (SD) age, weight, and total IgE level were 41.9 (9.4) years, 78.6 (15) kg, and 198.8 (169.2) IU/mL, respectively. 3 patients had mild, 6 had moderate and 1 had severe asthma as comorbidity. The mean (SD) duration of omalizumab treatment and polypectomy numbers were 9.2 (13.3) months and 2.9 (1.5), respectively. All patients had at least one polyp surgery. All sinonasal outcome parameters were significantly improved by the omalizumab treatment, also in subgroups with and without asthma. The median changes from baseline at the last visit date for omalizumab treatment were as follows: SNOT-22 score decreased from 98 to 19, NOSE score decreased from 100 to 20, the VAS for postnasal drip, rhinorrhea, nasal stuffiness, smell and sneeze decreased from 8 to 2, 8 to 2, 10 to 3, 10 to 2, 6 to 1, respectively (P < 0.001). Patients experienced no adverse reaction with omalizumab treatment. CONCLUSION: Omalizumab was an effective treatment in patients with recalcitrant CRSwNP with or without asthma. |
format | Online Article Text |
id | pubmed-9382317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | World Allergy Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-93823172022-08-24 Omalizumab is effective in nasal polyposis with or without asthma, a real-life study Tat, Tuğba Songül World Allergy Organ J Full-Length Article BACKGROUND: Chronic rhinosinusitis with nasal polyposis (CRSwNP) can be recalcitrant in some patients despite medical therapies and surgery and has higher morbidity. Omalizumab is a new treatment option for patients with CRSwNP. The aim of this study is to evaluate the efficacy and safety of omalizumab (anti-IgE antibody) in patients with CRSwNP. METHODS: The efficiency and adverse effects of omalizumab were evaluated based on the data extracted from medical records of patients with CRSwNP. Patients were evaluated monthly for efficacy and adverse reactions. Treatment efficacy was evaluated by visual analog scale (VAS) for rhinorrhea, postnasal drip, sneeze, smell, and nasal stuffiness complaints, sinonasal outcome test-22 (SNOT-22), and nose obstruction symptom evaluation (NOSE) score. RESULTS: 17 patients with CRSwNP formed our cohort. The mean (SD) age, weight, and total IgE level were 41.9 (9.4) years, 78.6 (15) kg, and 198.8 (169.2) IU/mL, respectively. 3 patients had mild, 6 had moderate and 1 had severe asthma as comorbidity. The mean (SD) duration of omalizumab treatment and polypectomy numbers were 9.2 (13.3) months and 2.9 (1.5), respectively. All patients had at least one polyp surgery. All sinonasal outcome parameters were significantly improved by the omalizumab treatment, also in subgroups with and without asthma. The median changes from baseline at the last visit date for omalizumab treatment were as follows: SNOT-22 score decreased from 98 to 19, NOSE score decreased from 100 to 20, the VAS for postnasal drip, rhinorrhea, nasal stuffiness, smell and sneeze decreased from 8 to 2, 8 to 2, 10 to 3, 10 to 2, 6 to 1, respectively (P < 0.001). Patients experienced no adverse reaction with omalizumab treatment. CONCLUSION: Omalizumab was an effective treatment in patients with recalcitrant CRSwNP with or without asthma. World Allergy Organization 2022-08-10 /pmc/articles/PMC9382317/ /pubmed/36017064 http://dx.doi.org/10.1016/j.waojou.2022.100670 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full-Length Article Tat, Tuğba Songül Omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
title | Omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
title_full | Omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
title_fullStr | Omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
title_full_unstemmed | Omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
title_short | Omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
title_sort | omalizumab is effective in nasal polyposis with or without asthma, a real-life study |
topic | Full-Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9382317/ https://www.ncbi.nlm.nih.gov/pubmed/36017064 http://dx.doi.org/10.1016/j.waojou.2022.100670 |
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