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Salivary Microbiome Relates to Neoadjuvant Immunotherapy Response in OSCC.
X X Wang1, Y T Liu1, J G Ren1,2
1State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
Oral squamous cell carcinoma patients with low salivary Eubacterium infirmum, Actinobaculum, and Selenomas (EAS) levels before treatment show poor response to immunotherapy. Low EAS may predict immunotherapy nonresponse in oral cancer.
Area of Science:
- Oncology
- Microbiome Research
- Immunotherapy
Background:
- Oral squamous cell carcinoma (OSCC) often presents at advanced stages with poor prognoses.
- Immunotherapy offers survival benefits but suffers from low response rates.
- The oral microbiome's role in tumor immunity and immunotherapy response remains under investigation.
Purpose of the Study:
- To explore the association between the salivary microbiome and immunotherapy response in OSCC patients.
- To identify potential salivary microbiome biomarkers predicting immunotherapy efficacy.
Main Methods:
- Salivary metagenome sequencing in 47 OSCC patients undergoing neoadjuvant immunotherapy (NAIT).
- Classification of patients into responders and nonresponders based on pathological outcomes.
- Development and validation of a nomogram predicting NAIT efficacy using salivary bacterial levels.
Main Results:
- Nonresponders had lower salivary microbiome species richness than responders pre-NAIT.
- Specific bacterial species, notably lower levels of Eubacterium infirmum, Actinobaculum, and Selenomas (EAS), were associated with nonresponse.
- Low salivary EAS levels correlated with reduced intratumoral immune cell infiltration and predicted nonresponse with an AUC of 0.81.
Conclusions:
- Salivary microbiome profiles differ between immunotherapy responders and nonresponders in OSCC patients prior to treatment.
- Low salivary EAS abundance is a potential predictive biomarker for identifying nonresponders to NAIT in OSCC.
- EAS-associated metabolic pathways may influence immunotherapy response in OSCC.
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