Biologics for chronic rhinosinusitis
- PMID: 32102112
- PMCID: PMC7043934
- DOI: 10.1002/14651858.CD013513.pub2
Biologics for chronic rhinosinusitis
Update in
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Biologics for chronic rhinosinusitis.Cochrane Database Syst Rev. 2021 Mar 12;3(3):CD013513. doi: 10.1002/14651858.CD013513.pub3. Cochrane Database Syst Rev. 2021. PMID: 33710614 Free PMC article.
Abstract
Background: This living systematic review is one of several Cochrane Reviews evaluating the medical management of patients with chronic rhinosinusitis. Chronic rhinosinusitis is common. It is characterised by inflammation of the nasal and sinus linings, nasal blockage, rhinorrhoea, facial pressure/pain and loss of sense of smell. It occurs with or without nasal polyps. 'Biologics' are medicinal products produced by a biological process. Monoclonal antibodies are one type, already evaluated in related inflammatory conditions (e.g. asthma and atopic dermatitis).
Objectives: To assess the effects of biologics for the treatment of chronic rhinosinusitis.
Search methods: The Cochrane ENT Information Specialist searched the Cochrane ENT Register; CENTRAL (2019, Issue 9); Ovid MEDLINE; Ovid Embase; Web of Science; ClinicalTrials.gov; ICTRP and additional sources for published and unpublished trials. The date of the search was 16 September 2019.
Selection criteria: Randomised controlled trials (RCTs) with at least three months follow-up comparing biologics (currently, monoclonal antibodies) against placebo/no treatment in patients with chronic rhinosinusitis.
Data collection and analysis: We used standard Cochrane methodological procedures. Our primary outcomes were disease-specific health-related quality of life (HRQL), disease severity and serious adverse events (SAEs). The secondary outcomes were avoidance of surgery, extent of disease (measured by endoscopic or computerised tomography (CT) score), generic HRQL and adverse events (nasopharyngitis, including sore throat). We used GRADE to assess the certainty of the evidence for each outcome.
Main results: We included eight RCTs. Of 986 adult participants, 984 had severe chronic rhinosinusitis with nasal polyps; 43% to 100% of participants also had asthma. Three biologics, with different targets, were evaluated: dupilumab, mepolizumab and omalizumab. All the studies were sponsored or supported by industry. Anti-IL-4Rα mAb (dupilumab) versusplacebo/no treatment (all receiving intranasal steroids) Three studies (784 participants) evaluated dupilumab. Disease-specific HRQL was measured with the SNOT-22 (score 0 to 110; minimal clinically important difference (MCID) 8.9 points). At 24 weeks, the SNOT-22 score was 19.61 points lower (better) in participants receiving dupilumab (mean difference (MD) -19.61, 95% confidence interval (CI) -22.54 to -16.69; 3 studies; 784 participants; high certainty). Symptom severity measured on a 0- to 10-point visual analogue scale (VAS) was 3.00 lower in those receiving dupilumab (95% CI -3.47 to -2.53; 3 studies; 784 participants; moderate certainty). The risk of serious adverse events may be lower in the dupilumab group (risk ratio (RR) 0.45, 95% CI 0.28 to 0.75; 3 studies; 782 participants; low certainty). The number of participants requiring nasal polyp surgery (actual or planned) during the treatment period is probably lower in those receiving dupilumab (RR 0.17, 95% CI 0.05 to 0.52; 2 studies; 725 participants; moderate certainty). Change in the extent of disease using the Lund Mackay computerised tomography (CT) score (0 to 24, higher = worse) was -7.00 (95% CI -9.61 to -4.39; 3 studies; 784 participants; high certainty), a large effect favouring the dupilumab group. The EQ-5D visual analogue scale (0 to 100, higher = better; MCID 8 points) was used to measure change in generic quality of life. The mean difference favouring dupilumab was 8.59 (95% CI 5.31 to 11.86; 2 studies; 706 participants; moderate certainty). There may be little or no difference in the risk of nasopharyngitis (RR 0.95, 95% CI 0.72 to 1.25; 3 studies; 783 participants; low certainty). Anti-IL-5 mAb (mepolizumab) versusplacebo/no treatment (all receiving intranasal steroids) Two studies (137 participants) evaluated mepolizumab. Disease-specific HRQL measured with the SNOT-22 at 25 weeks was 13.26 points lower (better) in participants receiving mepolizumab (95% CI -22.08 to -4.44; 1 study; 105 participants; low certainty; MCID 8.9). It is very uncertain whether there is a difference in s ymptom severity: on a 0- to 10-point VAS symptom severity was -2.03 lower in those receiving mepolizumab (95% CI -3.65 to -0.41; 1 study; 72 participants; very low certainty). It is very uncertain if there is difference in the risk of serious adverse events (RR 1.57, 95% CI 0.07 to 35.46; 2 studies; 135 participants, very low certainty). It is very uncertain whether or not the overall risk that patients still need surgery at trial end is lower in the mepolizumab group (RR 0.78, 95% CI 0.64 to 0.94; 2 studies; 135 participants; very low certainty). It is very uncertain whether mepolizumab reduces the extent of disease as measured by endoscopic nasal polyps score (scale range 0 to 8). The mean difference was 1.23 points lower in the mepolizumab group (MD -1.23, 95% -1.79 to -0.68; 2 studies; 137 participants; very low certainty). The difference in generic quality of life (EQ-5D) was 5.68 (95% CI -1.18 to 12.54; 1 study; 105 participants; low certainty), favouring the mepolizumab group. This difference is smaller than the MCID of 8 points. There may be little or no difference in the risk of nasopharyngitis (RR 0.73, 95% 0.36 to 1.47; 2 studies; 135 participants; low certainty). Anti-IgE mAb (omalizumab) versus placebo/no treatment (all receiving intranasal steroids) Three very small studies (65 participants) evaluated omalizumab. We are very uncertain about the effect of omalizumab on disease-specific HRQL, severe adverse events, extent of disease (CT scan scores), generic HRQL and adverse effects.
Authors' conclusions: In adults with severe chronic rhinosinusitis and nasal polyps, using regular topical nasal steroids, dupilumab improves disease-specific HRQL compared to placebo, and reduces the extent of the disease as measured on a CT scan. It probably also improves symptoms and generic HRQL and there is no evidence of an increased risk of serious adverse events. It may reduce the need for further surgery. There may be little or no difference in the risk of nasopharyngitis. In similar patients, mepolizumab may improve both disease-specific and generic HRQL. It is uncertain whether it reduces the need for surgery or improves nasal polyp scores. There may be little or no difference in the risk of nasopharyngitis. It is uncertain if there is a difference in symptom severity and the risk of serious adverse events. We are uncertain about the effects of omalizumab.
Copyright © 2020 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Conflict of interest statement
Lee‐Yee Chong: none known.
Patorn Piromchai: none known.
Steve Sharp: Steve Sharp's employer, the National Institute for Health and Care Excellence (NICE), has produced guidance on related topics such as sinusitis, which he has not contributed to.
Kornkiat Snidvongs: none known.
Carl Philpott: Carl Philpott has previously received consultancy fees for Acclarent, Navigant, Aerin Medical and Entellus, and is a trustee of the patient charity Fifth Sense. He is an investigator on a clinical trial that may be included in this review, but will have no role in the data extraction, risk of bias assessment or data analysis for this study.
Claire Hopkins: Claire Hopkins has participated in advisory boards for Olympus, Chordate, Smith & Nephew and Sanofi to provide expertise with regards to study design and outcome assessment, and interpretation of trial data. She is an investigator on a clinical trial that is included in this review, but had no role in the data extraction, risk of bias assessment or data analysis for this study (LIBERTY SINUS 24; LIBERTY SINUS 52).
Martin J Burton: Professor Martin Burton is joint Co‐ordinating Editor of Cochrane ENT, but had no role in the editorial process for this review.
Figures
References
References to studies included in this review
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MUSCA {published data only}
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- NCT02281318. Efficacy and safety study of mepolizumab adjunctive therapy in participants with severe eosinophilic asthma on markers of asthma control [A randomised, double‐blind, placebo‐controlled, parallel‐group, multi‐centre 24‐week study to evaluate the efficacy and safety of mepolizumab adjunctive therapy in subjects with severe eosinophilic asthma on markers of asthma control]. https://clinicaltrials.gov/show/nct02281318 (first received 3 November 2014). [CRS: 3545753]
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- Castro M, Zangrilli J, Wechsler ME, Bateman ED, Brusselle GG, Bardin P, et al. Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from two multicentre, parallel, double‐blind, randomised, placebo‐controlled, phase 3 trials. Lancet Respiratory Medicine 2015;3(5):355‐66. [CRS: 1797555; PUBMED: 25736990] - PubMed
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NCT02772419 {published data only}
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- NCT02772419. Study of benralizumab (KHK4563) in patients with eosinophilic chronic rhinosinusitis [A phase 2, double‐blind, placebo‐controlled study of benralizumab (KHK4563) in patients with eosinophilic chronic rhinosinusitis]. https://clinicaltrials.gov/show/NCT02772419 (first received 13 May 2016). [CENTRAL: CN‐01415166; CRS: 6978699]
NCT02799446 {published data only}
-
- NCT02799446. Effect of reslizumab in chronic rhinosinusitis [Efficacy of reslizumab for the treatment of chronic rhinosinusitis a double blind, randomized, placebo‐controlled, phase III trial]. https://clinicaltrials.gov/show/NCT02799446 (first received 14 June 2016). [CRS: 6978626]
NCT03450083 {published data only}
-
- NCT03450083. Benralizumab effect on severe chronic rhinosinusitis with eosinophilic polyposis [Benralizumab effect on severe chronic rhinosinusitis with eosinophilic polyposis: a phase II randomized placebo controlled trial]. https://clinicaltrials.gov/show/nct03450083 (first received 17 August 2017). [CRS: 8239610]
NCT03614923 {published data only}
-
- NCT03614923. Etokimab in adult patients with chronic rhinosinusitis with nasal polyps (CRSwNP) [A phase 2 double‐blind, placebo‐controlled multi‐dose study to investigate etokimab (ANB020) activity in adult patients with chronic rhinosinusitis with nasal polyps]. https://clinicaltrials.gov/show/NCT03614923 (first received 3 August 2018). [CRS: 9157986]
OSTRO {published data only}
-
- NCT03401229. Efficacy and safety study of benralizumab for patients with severe nasal polyposis [A multicenter, randomized, double‐blind, parallel‐group, placebo‐controlled phase 3 efficacy and safety study of benralizumab in patients with severe nasal polyposis]. https://clinicaltrials.gov/show/NCT03401229 (first received 17 January 2018). [CRS: 8275488]
POLYP 1 {unpublished data only}
-
- NCT03280550. A clinical trial of omalizumab in participants with chronic rhinosinusitis with nasal polyps [A phase III, randomized, multicenter, double‐blind, placebo‐controlled clinical trial of omalizumab in patients with chronic rhinosinusitis with nasal polyps]. https://clinicaltrials.gov/show/NCT03280550 (first received 12 September 2017). [CENTRAL: CN‐01415214; CRS: 6978602]
POLYP 2 {unpublished data only}
-
- NCT03280537. A clinical trial of omalizumab in participants with chronic rhinosinusitis with nasal polyps [A phase III, randomized, multicenter, double‐blind, placebo‐controlled clinical trial of omalizumab in patients with chronic rhinosinusitis with nasal polyps]. https://clinicaltrials.gov/show/NCT03280537 (first received 12 September 2017). [CENTRAL: CN‐01415096; CRS: 6977504]
SYNAPSE {published data only}
-
- EUCTR2016‐004255‐70‐SE. Effect of mepolizumab in severe bilateral nasal polyps [A randomised, double‐blind, parallel group PhIII study to assess the clinical efficacy and safety of 100 mg SC mepolizumab as an add on to maintenance treatment in adults with severe bilateral nasal polyps ‐ SYNAPSE (StudY in NAsal Polyps patients to assess the Safety and Efficacy of mepolizumab)]. https://www.clinicaltrialsregister.eu/ctr‐search/trial/2016‐004255‐70/SE (first received 4 October 2017). [CRS: 10787349]
-
- NCT03085797. Effect of mepolizumab in severe bilateral nasal polyps [A randomised, double‐blind, parallel group PhIII study to assess the clinical efficacy and safety of 100 mg SC mepolizumab AS an add on to maintenance treatment in adults with severe bilateral nasal polyps ‐ SYNAPSE (study in nasal polyps patients to assess the safety and efficacy of mepolizumab)]. https://clinicaltrials.gov/show/NCT03085797 (first received 21 March 2017). [CRS: 6978655]
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