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Human papilloma virus and p53 in head and neck cancer: clinical correlates and survival.

D J Haraf, E Nodzenski, D Brachman, R Mick, A Montag, D Graves, E E Vokes and R R Weichselbaum
D J Haraf
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E Nodzenski
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D Brachman
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R Mick
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A Montag
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D Graves
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E E Vokes
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R R Weichselbaum
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DOI:  Published April 1996
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Abstract

Recent studies have shown that p53 mutations are frequently found in cancer of the head and neck, whereas others have indicated that human papilloma virus (HPV) infection may be involved. Thus far, no studies have examined both p53 and HPV in the same patient population and correlated the results with clinical characteristics and outcome. The purpose of this study was to examine any interrelationship between p53 and HPV in patients with squamous cell carcinoma (SCC) of the head and neck. We also planned to correlate the experimental findings with clinical characteristics, known risk factors, and treatment outcome to determine whether any prognostic factors could be detected. Archival material from 66 patients with SCC of the head and neck were selected for study based on the availability of tissue from the primary tumors prior to treatment. A data base was constructed containing all clinical parameters at the time of diagnosis and risk factors. Genomic DNA was isolated and amplified using PCR, followed by SSCP analysis and direct genomic sequencing of all variants to detect p53 mutations. Two independent methods were used for HPV detection: (a) PCR amplification using primers homologous to the E6 region of HPV 16, 18, and 33, followed by RFLP analysis; and (b) PCR amplification with HPV L1 consensus primers, followed by triple restriction enzyme digestion. The results were entered into the data base for statistical analysis. Twenty-four percent of patients were found to have p53 mutations, and 18% were positive for HPV infection. Only one patient was positive for both. Tonsilar cancer was strongly correlated with HPV (P = 0.0001) and inversely correlated with p53 (P = 0.03). The only clinical parameter associated with p53 mutation was a trend toward a heavier smoking history. A subset analysis of the patients with tonsilar cancer revealed inverse correlations with smoking (P = 0. 015) and alcohol use (P = 0.05). Also, white patients with SCC of the tonsil were more likely to be HPV positive (P = 0.015). No significant relationships with outcome were detected with either p53 or HPV in the entire population. A subset analysis of patients with stage IV disease revealed that HPV infection was correlated with overall survival. This is the largest study to date to examine both p53 and HPV in patients with SCC of the head and neck. Our results suggest that HPV may be involved in the development of these cancers in patients without traditional risk factors and that HPV-related cancers are more prevalent in the white race.

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April 1996
Volume 2, Issue 4
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Human papilloma virus and p53 in head and neck cancer: clinical correlates and survival.
D J Haraf, E Nodzenski, D Brachman, R Mick, A Montag, D Graves, E E Vokes and R R Weichselbaum
Clin Cancer Res April 1 1996 (2) (4) 755-762;

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Human papilloma virus and p53 in head and neck cancer: clinical correlates and survival.
D J Haraf, E Nodzenski, D Brachman, R Mick, A Montag, D Graves, E E Vokes and R R Weichselbaum
Clin Cancer Res April 1 1996 (2) (4) 755-762;
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Clinical Cancer Research
eISSN: 1557-3265
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