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  4. Post-irradiation dysbiosis in patients with nasopharyngeal carcinoma having received radiotherapy – A pilot study
 
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Post-irradiation dysbiosis in patients with nasopharyngeal carcinoma having received radiotherapy – A pilot study

Journal
Oral Oncology
Date Issued
2024-07-01
Author(s)
YEN-TING LU  
DOI
10.1016/j.oraloncology.2024.106864
URI
https://www.scopus.com/pages/publications/85194942354
https://scholars.csmu.edu.tw/handle/123456789/32534
Abstract
Objective: To compare the changes in the sinonasal mucosa microbiome in patients with nasopharyngeal carcinoma (NPC) before and after radiotherapy (RT), and to explore the pathogenesis of post-irradiation chronic rhinosinusitis (PI-CRS) and its association with dysbiosis. Study Design: Prospective cohort study. Setting: Unicenter, Tertiary referral hospital. Methods: Included patients newly diagnosed with NPC. Samples of ostiomeatal complex mucosa were collected before and after RT. Microbiome analysis was conducted using 16S rRNA sequencing, and statistical analysis was performed. Subgroup analyses based on RT modality (proton therapy or photon therapy) Results: Total of 18 patients were enrolled in the study, with 62.1% receiving intensity-modulated proton therapy (IMPT). Corynebacterium was the most dominant genus identified in both the pre- and post-RT groups, with a visible increase in Staphylococcus and a decrease in Fusobacterium genus in post-RT group. Alpha-diversity did not significantly differ between groups, although the beta-diversity analysis revealed a dispersed microbiota in the post-RT group. The functional prediction indicated a higher relative abundance of taxonomies associated with biofilm formation in the post-RT group. The subgroup analysis revealed the above changes to be more significant in patients who received photon therapy (Intensity modulated radiation therapy, IMRT). Conclusions: This is the first study to analyze the microbiome of patients with NPC after IMPT. We identified similarities between the post-RT microenvironment and that reported in patients with CRS, with a more apparent change noted in patients treated with IMRT. Further investigation is required to further elucidate the pathogenesis of PI-CRS and its relationship to post-RT dysbiosis, particularly IMPT.
Type
journal article
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