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ISSN: 2161-119X

Otolaryngology: Open Access
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Platelet-to-Lymphocyte Ratio Might Predict the Response to Dupilumab Treatment for Patients with Nasal Polyposis

*Corresponding Author:

Received Date: Feb 28, 2025 / Published Date: Mar 30, 2025

Citation: Andrew B (2025) Platelet-To-Lymphocyte Ratio Might Predict the Response to Dupilumab Treatment for Patients with Nasal Polyposis. Otolaryngol (Sunnyvale) 15: 629.DOI: 10.4172/2161-119X.1000629

Copyright: © 2025 Andrew B. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 
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Abstract

Chronic rhinosinusitis with nasal polyposis (CRSwNP) is a debilitating inflammatory condition often resistant to conventional therapies, necessitating innovative treatment approaches such as biologics like dupilumab. Dupilumab, a monoclonal antibody targeting interleukin-4 receptor alpha, has demonstrated efficacy in reducing nasal polyp burden, yet response variability among patients highlights the need for predictive biomarkers. The platelet-to-lymphocyte ratio (PLR), a simple hematological marker of systemic inflammation, has emerged as a potential predictor of treatment outcomes in various inflammatory diseases. This study explores the hypothesis that pretreatment PLR might predict the response to dupilumab in CRSwNP patients. We conducted a retrospective analysis of 65 patients with CRSwNP treated with dupilumab, assessing pretreatment PLR and its association with total treatment response, defined as a post-treatment nasal polyp score (NPS) of 0. Results indicated that patients with a high PLR (>131.2) exhibited a 3.9-fold higher likelihood of achieving complete polyp resolution, independent of confounding factors such as age, sex, and comorbidities. These findings suggest that PLR could serve as a costeffective, accessible biomarker to stratify patients likely to benefit from dupilumab, though prospective validation is warranted to confirm its clinical utility.

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