ArticleClinical and translational radiation oncology2026
Motion-based tissue
Article in Clinical and translational radiation oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
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Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background and purpose: Proton radiotherapy is applied for various tumor sites, offering better dose distribution resulting in decreased excess radiation of healthy tissue. Furthermore, the biological effects of proton irradiation may be different from X-ray irradiation, depending on tumor characteristics. This is particularly relevant for head and neck squamous cell carcinoma (HNSCC), which displays high biological heterogeneity. However, this heterogeneous response to various radiation modalities is currently not included in clinical decision making due to lack of response prediction models. Materials and methods: Nine oral cavity tumor specimens were obtained after surgical resection, cut into thin slices, irradiated with both X-ray and protons, and cultured Results: Most tumors (five out of nine) showed similar response to proton and X-ray irradiation. However, in three tumors a significantly larger decrease in viability was measured upon proton irradiation. One of those tumors was homologous recombination deficient (HRD). The other two proton-sensitive tumors showed low numbers of infiltrating immune cells, including tumor infiltrating lymphocytes, while the most X-ray sensitive tumor had a particularly high immune cell infiltration. Conclusion: The
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