ArticleReports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology2025
Transcriptome-based model for predicting radiotherapy response in HNSCC patients.
Article in Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Multicentre study of inoperable HPV-negative head and neck cancer: a persistent real-world challenge.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2026Article
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17 authors.
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Abstract
Background: The main treatment method for head and neck squamous cell carcinomas (HNSCCs) is surgery in combination with radiotherapy or chemoradiation. However, the tumor heterogeneity and tumor microenvironment are issues of radiotherapy success. Due to this fact, the radioresistance process is not fully understood and seems to be a challenge for current oncology. Materials and methods: Radiotherapy treated HNSCC patients were divided into two groups based on the overall survival and excluding those with human papillomavirus (HPV) infection or treated with chemotherapy or targeted therapy. Next, groups were compared based on the clinical-pathological and transcriptome data (RNAseq) from The Cancer Genome Atlas Project (TCGA) using Gene Set Enrichment Analysis (GSEA) software and GraphPad Prism toll. Results: A model was created, consisting of two contrasting groups of patients: effective treatment group (ETG, n = 34) and ineffective treatment group (ITG, n = 31) for radiotherapy. Patients in the ITG group had a significantly shorter progression-free interval (PFI) than the ETG group, with a median of 266 days (p < 0.0001). Between the ETG and ITG groups, no differences (p > 0.05) were observed in clinical and pathological parameters, except perineural invasion (p = 0.0068) and the presence of a new tumor event after initial treatment (p < 0.0001). Molecular pathway analysis showed that ITG patients had statistically significantly increased expression of genes associated with DNA repair. Conclusions: We observed that our model, consisting of two groups, differed at the molecular level in genetic changes. Moreover, the presented model and its characterization showed that it was potentially useful for searching for potential biomarkers.
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