4.7 Article

Mepolizumab Improves Outcomes of Chronic Rhinosinusitis with Nasal Polyps in Severe Asthmatic Patients: A Multicentric Real-Life Study

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JOURNAL OF PERSONALIZED MEDICINE
卷 12, 期 8, 页码 -

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MDPI
DOI: 10.3390/jpm12081304

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chronic rhinosinusitis; nasal polyps; severe asthma; mepolizumab; SNOT-22; nasal polyp score; eosinophil; IL-5; biologics

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This study evaluated the effectiveness of mepolizumab in treating comorbid CRSwNP and severe asthma. The results showed significant improvements in SNOT-22 score, NP score, and blood eosinophil count after 12 months of treatment. Some patients experienced improvements in both clinical and endoscopic outcomes. Responders had higher baseline SNOT-22 score compared to nonresponders. Further studies are needed to supplement these preliminary findings.
Objective: The upcoming introduction of mepolizumab represents a promising treatment for chronic rhinosinusitis with nasal polyps (CRSwNP). The present study aimed to evaluate the effectiveness of mepolizumab on sinonasal outcomes of comorbid CRSwNP and severe asthma in a real-life setting. The primary endpoint was to evaluate changes in the SinoNasal Outcome Test (SNOT)-22 score, Nasal Polyp (NP) score, and blood eosinophil count during a 12-month treatment with mepolizumab. Secondary endpoints were to quantify mepolizumab's effects on the mentioned parameters, identify clinical variables influencing the degree of response to treatment, and portray responder and nonresponder patients. Methods: A multicentric retrospective no-profit observational study on severe asthmatic patients, treated with mepolizumab, and comorbid CRSwNP was conducted. All patients were followed for at least 12 months. SNOT-22 score, NP score, and blood eosinophil count (and other CRS-specific variables) were collected at baseline and after 12 months. Results: Forty-three patients were included. A statistically significant reduction was observed for SNOT-22 score (mean t0 SNOT-22 54.8 +/- 25.9; mean t12 SNOT-22 31.5 +/- 21.3, p < 0.0001), NP score (median t0 NPS 3 (IQR 3); median t12 NPS 2 (IQR 4), p < 0.0001), and blood eosinophil count (mean t0 blood eosinophils 804.7 +/- 461.5 cell/mu L; mean t12 blood eosinophils 107.5 +/- 104.6 cell/mu L, p < 0.0001) after 12 months of treatment. Twenty patients (47%) gained improvement both in clinical and endoscopic outcome. Mepolizumab responder patients presented a t0 SNOT-22 significantly higher than nonresponders (p = 0.0011). Conclusions: Mepolizumab improved CRSwNP outcomes in a population of severe asthmatic patients. No clinical feature emerged to outline the profile of a typical responder patient, except for baseline SNOT-22 score, which seemed to affect the response to treatment. Further studies would be necessary to supplement these preliminary evaluations.

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