Publication

Prognostic biomarkers in patients with human immunodeficiency virus-positive disease with head and neck squamous cell carcinoma

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Last modified
  • 05/15/2025
Type of Material
Authors
    Hongzheng Zhang, Emory UniversitySungjin Kim, Cedars Sinai Medical CenterZhengjia Chen, Emory UniversitySreenivas Nannapaneni, Emory UniversityAmy Chen, Emory UniversityCharles Moore, Emory UniversityGabriel Sica, Emory UniversityMarina Mosunjac, Emory UniversityMinhly Nguyen, Emory UniversityGypsyamber D'Souza, Johns Hopkins Bloomberg School of Public HealthThomas E. Carey, University of MichiganLisa A. Peterson, University of MichiganJonathan B. McHugh, University of MichiganMartin Graham, University of MichiganChristine M. Komarck, University of MichiganGregory T. Wolf, University of MichiganHeather M. Walline, University of MichiganGeorgia Chen, Emory UniversityNabil Saba, Emory UniversityDong Shin, Emory University
Language
  • English
Date
  • 2017-12-01
Publisher
  • Wiley: 12 months
Publication Version
Copyright Statement
  • © 2017 Wiley Periodicals, Inc.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1043-3074
Volume
  • 39
Issue
  • 12
Start Page
  • 2433
End Page
  • 2443
Grant/Funding Information
  • The study was supported by the NCI Head and Neck Cancer SPORE Consortium Supplement (3P50DE019032–14S1).
Supplemental Material (URL)
Abstract
  • Background: We examined the prognostic value of a panel of biomarkers in patients with squamous cell carcinoma of the head and neck (SCCHN) who were human immunodeficiency virus (HIV) positive (HIV-positive head and neck cancer) and HIV negative (HIV-negative head and neck cancer). Methods: Tissue microarrays (TMAs) were constructed using tumors from 41 disease site-matched and age-matched HIV-positive head and neck cancer cases and 44 HIV-negative head and neck cancer controls. Expression of tumor biomarkers was assessed by immunohistochemistry (IHC) and correlations examined with clinical variables. Results: Expression levels of the studied oncogenic and inflammatory tumor biomarkers were not differentially regulated by HIV status. Among patients with HIV-positive head and neck cancer, laryngeal disease site (P =.003) and Clavien-Dindo classification IV (CD4) counts <200 cells/μL (P =.01) were associated with poor prognosis. Multivariate analysis showed that p16 positivity was associated with improved overall survival (OS; P <.001) whereas increased expression of transforming growth factor-beta (TGF-β) was associated with poor clinical outcome (P =.001). Conclusion: Disease site has significant effect on the expression of biomarkers. Expression of tumor TGF-β could be a valuable addition to the conventional risk stratification equation for improving head and neck cancer disease management strategies.
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Research Categories
  • Biology, Biostatistics
  • Health Sciences, Medicine and Surgery

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