論文

国際誌
2021年7月

Prognostic significance of hypoxia-inducible factor-1α expression in advanced pharyngeal cancer without human papillomavirus infection.

The Journal of laryngology and otology
  • S Agena
  • H Hirakawa
  • T Ikegami
  • H Kinjyo
  • N Kise
  • H Maeda
  • J Uezato
  • S Kondo
  • A Kiyuna
  • Y Yamashita
  • N Hasegawa
  • M Suzuki
  • A Ganaha
  • 全て表示

135
7
開始ページ
625
終了ページ
633
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1017/S0022215121001468

OBJECTIVE: This study aimed to clarify the association between both hypoxia-inducible factor-1α and glucose transporter type-1 expression and survival outcome in advanced pharyngeal cancer without human papillomavirus infection. METHOD: Twenty-five oropharyngeal and 55 hypopharyngeal cancer patients without human papillomavirus infection were enrolled. All patients had stage III-IV lesions and underwent concurrent chemoradiotherapy or surgery. Hypoxia-inducible factor-1α and glucose transporter type-1 expression were investigated in primary lesions by immunohistochemistry. RESULTS: There were 41 and 39 cases with low and high hypoxia-inducible factor-1α expression, and 28 and 52 cases with low and high glucose transporter type-1 expression, respectively. There was no significant correlation between hypoxia-inducible factor-1α and glucose transporter type-1 expression. In univariate analysis, nodal metastasis, clinical stage and high hypoxia-inducible factor-1α expression, but not glucose transporter type-1 expression, predicted significantly worse prognosis. In multivariate analysis, hypoxia-inducible factor-1α overexpression was significantly correlated with poor overall survival, disease-specific survival and recurrence-free survival. CONCLUSION: High hypoxia-inducible factor-1α expression was an independent risk factor for poor prognosis for advanced human papillomavirus-unrelated pharyngeal cancer.

リンク情報
DOI
https://doi.org/10.1017/S0022215121001468
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/34108057
ID情報
  • DOI : 10.1017/S0022215121001468
  • PubMed ID : 34108057

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