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Oral Human Papillomavirus Infection Before and After Treatment for Human Papillomavirus 16-Positive and Human Papillomavirus 16-Negative Head and Neck Squamous Cell Carcinoma

  1. Author:
    Agrawal, Y.
    Koch, W. M.
    Xiao, W.
    Westra, W. H.
    Trivett, A. L.
    Symer, D. E.
    Gillison, M. L.
  2. Author Address

    Agrawal, Yuri, Koch, Wayne M.] Johns Hopkins Univ Hosp, Dept Otolaryngol Head & Neck Surg, Baltimore, MD 21287 USA. [Westra, William H.] Johns Hopkins Univ Hosp, Dept Pathol, Baltimore, MD 21287 USA. [Xiao, Weihong, Gillison, Maura L.] Johns Hopkins Kimmel Comprehens Canc Ctr, Div Viral Oncol, Baltimore, MD USA. [Trivett, Anna L.; Symer, David E.] Natl Canc Inst, Basic Res Lab, Frederick, MD USA.
    1. Year: 2008
  1. Journal: Clinical Cancer Research
    1. 14
    2. 21
    3. Pages: 7143-7150
  2. Type of Article: Article
  1. Abstract:

    Purpose: Oral human papillomavirus (HPV) infection is a risk factor for head and neck squamous cell carcinoma (HNSCC), and is a concern for patients with HPV-positive HNSCC and their partners. The prevalence of oral HPV infection before and after cancer therapy was investigated among patients with HPV16-positive and HPV16-negative HNSCC. Experimental Design: Serial oral rinse samples (ORS) were collected from a cohort of 135 HNSCC cases as frequently as every 3 months for up to 3 years. Tumor HPV status was determined by HPV16 in situ hybridization. HPV was detected in ORS by consensus PCR and line blot hybridization. The HPV16 variants in positive oral rinse - tumor pairs were determined by sequencing. The odds of oral HPV infection among HPV16-positive and HPV16-negative cases were compared by use of generalized estimating equations. Results: Patients were followed for a median of 21 months and provided a median of 4 samples. Forty-four of 135 patients had HPV16-positive tumors. HPV16-positive cases were more likely than HPV16-negative cases to have an oral HPV infection detected before (odds ratio, 8.6, 95% confidence interval, 3.5-21) and after therapy (OR, 2.9, 95% confidence interval, 1.1-7.4). Oral infections by HPV16 and other high-risk, but not low-risk, types were more common among HPV16-positive cases both before and after therapy. Most HPV16 variants in ORS were European, unique, and identical to that in the tumor. Persistence of a type-specific oral infection was demonstrable for as long as 5 years. Conclusion: Oral high-risk HPV infections are more frequent among patients with HPV16-positive than HPV16-negative HNSCC, consistent with a behavioral and/or biological disposition to infection

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External Sources

  1. PMID: 18981014

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