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Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients

OBJECTIVE: The introduction of monoclonal antibody (mAb) therapies represents a promising treatment for refractory chronic rhinosinusitis (CRS). We assessed the effects of selected mAbs (omalizumab, mepolizumab, benralizumab) on CRS in severe asthmatic patients in a real-life setting. METHODS: A pro...

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Autores principales: Bandi, Francesco, Gallo, Stefania, Preti, Andrea, Mozzanica, Francesco, Visca, Dina, Marelli, Margherita, Maddalone, Enrico, Gambarini, Cinzia, Vaghi, Adriano, Spanevello, Antonio, Castelnuovo, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore Srl 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889250/
https://www.ncbi.nlm.nih.gov/pubmed/33558772
http://dx.doi.org/10.14639/0392-100X-N0716
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author Bandi, Francesco
Gallo, Stefania
Preti, Andrea
Mozzanica, Francesco
Visca, Dina
Marelli, Margherita
Maddalone, Enrico
Gambarini, Cinzia
Vaghi, Adriano
Spanevello, Antonio
Castelnuovo, Paolo
author_facet Bandi, Francesco
Gallo, Stefania
Preti, Andrea
Mozzanica, Francesco
Visca, Dina
Marelli, Margherita
Maddalone, Enrico
Gambarini, Cinzia
Vaghi, Adriano
Spanevello, Antonio
Castelnuovo, Paolo
author_sort Bandi, Francesco
collection PubMed
description OBJECTIVE: The introduction of monoclonal antibody (mAb) therapies represents a promising treatment for refractory chronic rhinosinusitis (CRS). We assessed the effects of selected mAbs (omalizumab, mepolizumab, benralizumab) on CRS in severe asthmatic patients in a real-life setting. METHODS: A prospective observational study on severe asthmatic patients, treated with 3 different mAb (omalizumab, mepolizumab, benralizumab), and comorbid CRS was conducted. All patients were followed for 52 weeks. The degree of nasal control, SinoNasal Outcome Test (SNOT) 22, Nasal Polyp Score (NPS), Lund Kennedy Score (LKS) were collected at baseline and at 52-week. RESULTS: 40 patients (33 with nasal polyps) were studied. 33 patients (82.5%) had uncontrolled nasal disease at baseline, and 15 (37.5%) were uncontrolled after 52 weeks. Significant improvement was observed for SNOT 22 (P < 0.001), SNOT 1-12 (P < 0.001) and degree of nasal control (P < 0.001). Differences in NPS (P = 0.130) and LKS (P = 0.124) were not significant. Net change in the above-mentioned parameters among the three treatment groups was not significantly different. CONCLUSIONS: The study shows an improvement of nasal symptoms after 52 weeks of mAb treatment, which was not associated with significant improvement of endoscopic findings. Larger studies are needed to assess the real-life efficacy of mAbs in CRS.
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spelling pubmed-78892502021-02-25 Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients Bandi, Francesco Gallo, Stefania Preti, Andrea Mozzanica, Francesco Visca, Dina Marelli, Margherita Maddalone, Enrico Gambarini, Cinzia Vaghi, Adriano Spanevello, Antonio Castelnuovo, Paolo Acta Otorhinolaryngol Ital Rhinology OBJECTIVE: The introduction of monoclonal antibody (mAb) therapies represents a promising treatment for refractory chronic rhinosinusitis (CRS). We assessed the effects of selected mAbs (omalizumab, mepolizumab, benralizumab) on CRS in severe asthmatic patients in a real-life setting. METHODS: A prospective observational study on severe asthmatic patients, treated with 3 different mAb (omalizumab, mepolizumab, benralizumab), and comorbid CRS was conducted. All patients were followed for 52 weeks. The degree of nasal control, SinoNasal Outcome Test (SNOT) 22, Nasal Polyp Score (NPS), Lund Kennedy Score (LKS) were collected at baseline and at 52-week. RESULTS: 40 patients (33 with nasal polyps) were studied. 33 patients (82.5%) had uncontrolled nasal disease at baseline, and 15 (37.5%) were uncontrolled after 52 weeks. Significant improvement was observed for SNOT 22 (P < 0.001), SNOT 1-12 (P < 0.001) and degree of nasal control (P < 0.001). Differences in NPS (P = 0.130) and LKS (P = 0.124) were not significant. Net change in the above-mentioned parameters among the three treatment groups was not significantly different. CONCLUSIONS: The study shows an improvement of nasal symptoms after 52 weeks of mAb treatment, which was not associated with significant improvement of endoscopic findings. Larger studies are needed to assess the real-life efficacy of mAbs in CRS. Pacini Editore Srl 2021-01-21 2020-12 /pmc/articles/PMC7889250/ /pubmed/33558772 http://dx.doi.org/10.14639/0392-100X-N0716 Text en Società Italiana di Otorinolaringoiatria e Chirurgia Cervico-Facciale, Rome, Italy https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en This is an open access article distributed in accordance with the CC-BY-NC-ND (Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International) license. The article can be used by giving appropriate credit and mentioning the license, but only for non-commercial purposes and only in the original version. For further information: https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en
spellingShingle Rhinology
Bandi, Francesco
Gallo, Stefania
Preti, Andrea
Mozzanica, Francesco
Visca, Dina
Marelli, Margherita
Maddalone, Enrico
Gambarini, Cinzia
Vaghi, Adriano
Spanevello, Antonio
Castelnuovo, Paolo
Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
title Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
title_full Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
title_fullStr Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
title_full_unstemmed Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
title_short Effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
title_sort effects of biological therapies on chronic rhinosinusitis in severe asthmatic patients
topic Rhinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889250/
https://www.ncbi.nlm.nih.gov/pubmed/33558772
http://dx.doi.org/10.14639/0392-100X-N0716
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