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Type 2 Biomarkers for the Indication and Response to Biologics in CRSwNP
Cui-Lian Guo1,2,3, Fei-Fan Liu1,2,3, De-Yun Wang4
1Department of Otolaryngology-Head and Neck Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, Wuhan, 430030, People's Republic of China.
Purpose Of Review:
Three biologics targeting type 2 inflammation have been approved for the treatment of severe and uncontrolled chronic rhinosinusitis with nasal polyps (CRSwNP). Nevertheless, around 40-60% of patients do not respond well to these biological treatments. Selecting appropriate patients is crucial to improve treatment outcome of biologics. This review summarizes the literature data on type 2 biomarkers, with a specific focus on the indication to biologics for severe CRSwNP.
Recent Findings:
No consensus has been reached on how to define mucosal type 2 inflammation in CRSwNP. Clinical markers (e.g., 22-item Sino-nasal Outcome Test (SNOT-22) score, Lund-Mackay CT score (LMS), ethmoid/maxillary sinus CT score, and CT-radiomics), nasal secretion biomarkers (e.g., eosinophil cationic protein and interleukin-5), blood and nasal cytology eosinophil counts, and nasal swab eosinophil peroxidase activity have been reported to be associated with type 2 inflammation in CRSwNP. The time duration since the last surgery, SNOT-22 score at 1 week of treatment, and baseline serum osteoprotegerin levels might indicate the response to dupilumab. LMS and asthma control test scores were found to have moderate predictive value for acceptable improvement after 24-week treatment of omalizumab. High blood eosinophil levels at baseline were associated with treatment response to mepolizumab and benralizumab. Although several clinical and biological markers might be associated with type 2 inflammation and response to biologics in patients with CRSwNP, their validity requires further investigation. Identifying clinically applicable biomarkers for biologic treatment holds significant promise for advancing personalized approaches to biologics and optimizing treatment outcomes for patients with CRSwNP.
Insights
Identifying type 2 biomarkers is key for effective biologic treatment in severe chronic rhinosinusitis with nasal polyps (CRSwNP). This review explores clinical and biological markers to personalize therapy and improve patient outcomes.
Area of Science:
- Immunology
- Otolaryngology
- Pharmacology
Background:
- Severe chronic rhinosinusitis with nasal polyps (CRSwNP) affects many patients, with limited response to current biologic therapies targeting type 2 inflammation.
- Approximately 40-60% of CRSwNP patients do not achieve optimal outcomes with existing biologics.
- Personalized patient selection is essential to enhance the efficacy of biologic treatments.
Purpose of the Study:
- To review and summarize literature data on type 2 biomarkers relevant to severe CRSwNP.
- To focus on the indication of biologics for CRSwNP based on identified biomarkers.
- To explore the potential of biomarkers in predicting treatment response.
Main Methods:
- Literature review of studies investigating type 2 inflammation markers in CRSwNP.
- Analysis of clinical markers such as Sino-nasal Outcome Test (SNOT-22) and Lund-Mackay CT score (LMS).
- Evaluation of biological markers including blood and nasal eosinophil counts, and inflammatory mediators.
Main Results:
- No definitive consensus exists for defining mucosal type 2 inflammation in CRSwNP.
- Various clinical and biological markers show association with type 2 inflammation and biologic response.
- Specific markers like baseline blood eosinophil counts may predict response to certain biologics (mepolizumab, benralizumab).
Conclusions:
- Several potential biomarkers for type 2 inflammation and biologic response in CRSwNP require further validation.
- Identifying reliable biomarkers is crucial for personalized medicine approaches in CRSwNP treatment.
- Optimizing biologic therapy selection can significantly improve treatment outcomes for patients with CRSwNP.
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