Monday, June 18, 2012

Study examines chronic inflammation in oral cavity and HPV status of head and neck cancers

Study examines chronic inflammation in oral cavity and HPV status of head and neck cancers [ Back to EurekAlert! ] Public release date: 18-Jun-2012
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Contact: Sara Saldi
saldi@buffalo.edu
716-645-4593
JAMA and Archives Journals

CHICAGO Among patients with head and neck squamous cell carcinomas, a history of chronic inflammation in the mouth (periodontitis, i.e. gum disease) may be associated with an increased risk of tumors positive for human papillomavirus (HPV), according to a report published Online First by Archives of Otolaryngology Head & Neck Surgery, a JAMA Network publication.

The National Cancer Institute has reported a steady increase in the prevalence of oropharyngeal cancers in the United States since 1973, despite a significant decline in tobacco use since 1965, according to background information in the study. Similar trends have been recognized worldwide, and the authors note that the increase has mainly been attributed to oral HPV infection.

Mine Tezal, D.D.S., Ph.D., of the University at Buffalo, and colleagues evaluated data from 124 patients diagnosed with primary squamous cell carcinoma (SCC) of the oral cavity, oropharynx, and larynx between 1999 and 2007 for whom tissue samples and dental records were available.

Of the 124 primary cases of head and neck squamous cell carcinoma, 31 (25 percent) were located in the oral cavity, 49 (39.5 percent) in the oropharynx and 44 (35.5 percent) in the larynx. Fifty (40.3 percent) of the 124 tumor samples were positive for HPV-16 DNA. The authors found that a higher percentage of oropharyngeal cancers were HPV-positive (65.3 percent) compared with oral cavity (29 percent) and laryngeal (20.5 percent) cancers.

Periodontitis history was assessed by alveolar bone loss (ABL) in millimeters from available dental records. Patients with HPV-positive tumors had significantly higher ABL compared with patients with HPV-negative tumors. Each millimeter of ABL was associated with an increased odds of HPV-positive tumor status 2.6 times after adjustment for other factors. The strength of this association was greater among patients with oropharyngeal SCC compared with those with oral cavity SCC and laryngeal SCC.

"Periodontitis is easy to detect and may represent a clinical high-risk profile for oral HPV infection," the authors conclude. "Prevention or treatment of sources of inflammation in the oral cavity may be a simple yet effective way to reduce the acquisition and persistence of oral HPV infection."

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(Arch Otolaryngol Head Neck Surg. Published online June 18, 2012. doi:10.1001/archoto.2012.873. Available pre-embargo to the media at www.media.jamanetwork.com.)

Editor's Note: This study was supported by grants from the National Cancer Institute and from the National Institute of Dental and Craniofacial Research. Please see the article for additional information, including other authors, author contributions and affiliations, financial disclosures, funding and support, etc.

To contact Mine Tezal, D.D.S., Ph.D., call Sara Saldi at 716-645-4593 or email saldi@buffalo.edu.



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Study examines chronic inflammation in oral cavity and HPV status of head and neck cancers [ Back to EurekAlert! ] Public release date: 18-Jun-2012
[ | E-mail | Share Share ]

Contact: Sara Saldi
saldi@buffalo.edu
716-645-4593
JAMA and Archives Journals

CHICAGO Among patients with head and neck squamous cell carcinomas, a history of chronic inflammation in the mouth (periodontitis, i.e. gum disease) may be associated with an increased risk of tumors positive for human papillomavirus (HPV), according to a report published Online First by Archives of Otolaryngology Head & Neck Surgery, a JAMA Network publication.

The National Cancer Institute has reported a steady increase in the prevalence of oropharyngeal cancers in the United States since 1973, despite a significant decline in tobacco use since 1965, according to background information in the study. Similar trends have been recognized worldwide, and the authors note that the increase has mainly been attributed to oral HPV infection.

Mine Tezal, D.D.S., Ph.D., of the University at Buffalo, and colleagues evaluated data from 124 patients diagnosed with primary squamous cell carcinoma (SCC) of the oral cavity, oropharynx, and larynx between 1999 and 2007 for whom tissue samples and dental records were available.

Of the 124 primary cases of head and neck squamous cell carcinoma, 31 (25 percent) were located in the oral cavity, 49 (39.5 percent) in the oropharynx and 44 (35.5 percent) in the larynx. Fifty (40.3 percent) of the 124 tumor samples were positive for HPV-16 DNA. The authors found that a higher percentage of oropharyngeal cancers were HPV-positive (65.3 percent) compared with oral cavity (29 percent) and laryngeal (20.5 percent) cancers.

Periodontitis history was assessed by alveolar bone loss (ABL) in millimeters from available dental records. Patients with HPV-positive tumors had significantly higher ABL compared with patients with HPV-negative tumors. Each millimeter of ABL was associated with an increased odds of HPV-positive tumor status 2.6 times after adjustment for other factors. The strength of this association was greater among patients with oropharyngeal SCC compared with those with oral cavity SCC and laryngeal SCC.

"Periodontitis is easy to detect and may represent a clinical high-risk profile for oral HPV infection," the authors conclude. "Prevention or treatment of sources of inflammation in the oral cavity may be a simple yet effective way to reduce the acquisition and persistence of oral HPV infection."

###

(Arch Otolaryngol Head Neck Surg. Published online June 18, 2012. doi:10.1001/archoto.2012.873. Available pre-embargo to the media at www.media.jamanetwork.com.)

Editor's Note: This study was supported by grants from the National Cancer Institute and from the National Institute of Dental and Craniofacial Research. Please see the article for additional information, including other authors, author contributions and affiliations, financial disclosures, funding and support, etc.

To contact Mine Tezal, D.D.S., Ph.D., call Sara Saldi at 716-645-4593 or email saldi@buffalo.edu.



[ Back to EurekAlert! ] [ | E-mail | Share Share ]

?


AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert! system.


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