Prognostic histological markers in oral tongue squamous cell carcinoma patients treated with (chemo)radiotherapy

Author:

Hyytiäinen Aini12,Mroueh Rayan34,Peltonen Johanna12,Wennerstrand Pia12,Mäkitie Antti356,Al‐Samadi Ahmed12,Ventelä Sami789,Salo Tuula12101112

Affiliation:

1. Department of Oral and Maxillofacial Diseases University of Helsinki Helsinki Finland

2. Translational Immunology Research Program, Faculty of Medicine University of Helsinki Helsinki Finland

3. Department of Otorhinolaryngology ‐ Head and Neck Surgery University of Helsinki and HUS Helsinki University Hospital Helsinki Finland

4. Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer and Research Helsinki Finland

5. Research Program in Systems Oncology, Faculty of Medicine University of Helsinki Helsinki Finland

6. Division of Ear, Nose and Throat Diseases, Department of Clinical Sciences, Intervention and Technology Karolinska Institutet and Karolinska Hospital Stockholm Sweden

7. Turku Bioscience Centre University of Turku and Åbo Akademi University Turku Finland

8. Department for Otorhinolaryngology, Head and Neck Surgery University of Turku and Turku University Hospital Turku Finland

9. FICAN West Cancer Centre Turku Finland

10. Cancer and Translational Medicine Research Unit University of Oulu Oulu Finland

11. Medical Research Center Oulu University Hospital Oulu Finland

12. Department of Pathology Helsinki University Hospital (HUS) Helsinki Finland

Abstract

Treatment of oral tongue squamous cell carcinoma (OTSCC) frequently includes surgery with postoperative radiotherapy (RT) or chemoradiotherapy (CRT). Resistance to RT or CRT remains a major clinical challenge and highlights the need to identify predictive markers for it. We included 71 OTSCC patients treated with surgery combined with RT or CRT. We evaluated the association between tumor budding, tumor–stroma ratio (TSR), depth of invasion (DOI), tumor‐infiltrating lymphocytes (TILs), hypoxia‐inducible factor‐1alpha (HIF‐1alpha) expression, octamer‐binding transcription factor 4 (OCT4) expression, high‐endothelial venules (HEVs), and disease‐free survival (DFS) using uni‐ and multivariate analyses. No significant association was observed between the different histological and molecular markers (TSR, DOI, TILs, HEV, HIF‐1alph, OCT4) and DFS. However, an associative trend between DOI, budding, and DFS was noted. Further studies with larger cohorts are needed to explore the prognostic value of DOI and budding for OTSCC patients treated with postoperative RT or CRT.

Publisher

Wiley

Subject

Microbiology (medical),General Medicine,Immunology and Allergy,Pathology and Forensic Medicine

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