Dupilumab associated with "highly favorable" outcomes in Type 2 Chronic Rhinosinusitis
Switzerland: A recent study published in Allergy, European Journal of Allergy and Clinical Immunology, predicted treatment outcome as "highly favorable" after one-week treatment of Type 2 Chronic Rhinosinusitis (T2CRS) patients with dupilumab.
On 26 June 2019, the US Food and Drug Administration approved Dupixent (dupilumab) to treat chronic rhinosinusitis in adults with nasal polyps. The approval was granted to Regeneron Pharmaceuticals. Polyps are growths on the inner lining of the sinuses. The prolonged inflammation of sinuses and nasal cavities often accompanies nasal polyps in T2CRS with no clarity on serological markers.
Dupilumab is the first-line treatment in such cases, mainly where nasal polyps are not controlled by intranasal steroids and require surgery and oral steroids. No data exist on factors that predict outcomes in dupilumab treatment.
Against the above background, a study was conducted by Lead researcher Soyka et al. with co-researcher Ryser to clinically assess ultra-short- and short-term outcomes for up to 90 days in patients on dupilumab treatment. The treatment response was identified using the clinical and serological markers, and the comparison was made with healthy controls (HC).
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