Preliminary insights into the impact of primary radiochemotherapy on the salivary microbiome in head and neck squamous cell carcinoma

• Published in: Scientific reports Vol. 10; no. 1; p. 16582
• Main Authors: Kumpitsch, Christina, Moissl-Eichinger, Christine, Pock, Jakob, Thurnher, Dietmar, Wolf, Axel
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 06.10.2020
• Subjects: 631/326/2565/2134; 631/67/1059/485; 631/67/1059/99; 692/4028/67/1536; Adult; Aged; Candida - genetics; Candida - isolation & purification; Chemoradiotherapy; Female; Head and Neck Neoplasms - microbiology; Head and Neck Neoplasms - therapy; Healthy Volunteers; High-Throughput Nucleotide Sequencing; Humanities and Social Sciences; Humans; Male; Microbiota - drug effects; Microbiota - genetics; Microbiota - radiation effects; Middle Aged; multidisciplinary; RNA, Ribosomal, 16S - genetics; Saliva - microbiology; Science; Science (multidisciplinary); Squamous Cell Carcinoma of Head and Neck - microbiology; Squamous Cell Carcinoma of Head and Neck - therapy
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-73515-0

Squamous cell carcinoma is the most common type of throat cancer. Treatment options comprise surgery, radiotherapy, and/or chemo(immuno)therapy. The salivary microbiome is shaped by the disease, and likely by the treatment, resulting in side effects caused by chemoradiation that severely impair patients’ well-being. High-throughput amplicon sequencing of the 16S rRNA gene provides an opportunity to investigate changes in the salivary microbiome in health and disease. In this preliminary study, we investigated alterations in the bacterial, fungal, and archaeal components of the salivary microbiome between healthy subjects and patients with head and neck squamous cell carcinoma before and close to the end point of chemoradiation (“after”). We enrolled 31 patients and 11 healthy controls, with 11 patients providing samples both before and after chemoradiation. Analysis revealed an effect on the bacterial and fungal microbiome, with a partial antagonistic reaction but no effects on the archaeal microbial community. Specifically, we observed an individual increase in Candida signatures following chemoradiation, whereas the overall diversity of the microbial and fungal signatures decreased significantly after therapy. Thus, our study indicates that the patient microbiome reacts individually to chemoradiation but has potential for future optimization of disease diagnostics and personalized treatments.