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

Aini Hyytiäinen, Rayan Mroueh, Johanna Peltonen, Pia Wennerstrand, Antti Mäkitie, Ahmed Al-Samadi, Sami Ventelä, Tuula Salo*

*Korresponderande författare för detta arbete

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

Sammanfattning

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.
OriginalspråkEngelska
Sidor (från-till)142-151
Antal sidor10
TidskriftAPMIS
Volym131
Nummer4
DOI
StatusPublicerad - apr. 2023
MoE-publikationstypA1 Tidskriftsartikel-refererad

Finansiering

The project was funded by the Victoriastiftelsen Foundation, Orion Research Foundation, Sigrid Jusélius Foundation and Helsinki University Hospital Research Funds.

FinansiärerFinansiärsnummer
Victoriastiftelsen Foundation
Hospital District of Helsinki and Uusimaa
Sigrid Jusélius Stiftelse
Orionin Tutkimussäätiö

    Nyckelord

    • Oral cancer
    • radioresistance
    • prognostic marker
    • octamer-binding transcription factor 4
    • hypoxia-inducible factor-1 alpha
    • high-endothelial venules
    • chemoresistance

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