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DOI 10.1016/j.anndiagpath.2011.07.003

Медицинская библиотека · Annals of diagnostic pathology · 2011

Changing trends in human papillomavirus-associated head and neck squamous cell carcinoma.

Wang Xiaohong Iris, Thomas Jaiyeola, Zhang Songlin

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Head and neck squamous cell carcinoma (HNSCC) continues to be a significant disease with varying rates of incidence and mortality worldwide. Numerous studies have demonstrated that human papillomavirus (HPV) is etiologically linked with a subset of HNSCC, independent of tobacco and alcohol use. This subset of tumor shows increased sensitivity to radiation therapy and association with better outcomes. The study aims to determine the HPV burden and trend among patients with HNSCC in the southern region of the United States over the past 10 years. Of 142 cases from 2000 to 2004, 18 (13%) were positive for high-risk HPV. Nine of these were oropharyngeal tumors, including 4 cases from the tonsil. These constitute 38% (9/24) of all oropharyngeal tumors and 57% (4/7) of tonsillar tumors. Of 35 cases from 2009 to 2010, 14 (40%) were positive for high-risk HPV. Thirteen of these were oropharyngeal tumors, including 9 cases from the tonsil. These constitute 59% (13/23) of oropharyngeal tumors and 64% (9/14) of tonsillar tumors. When data from the 2 periods are combined, the results show that African American patients are less likely to have HPV-associated disease compared with white patients (9% vs 22%). Human papillomavirus-positive and oropharyngeal HNSCC are more likely to be nonkeratinizing (P < .0001). In conclusion, the HPV detection rate in oropharyngeal squamous cell carcinoma increased from 38% to 59% between the 2000-to-2004 and 2009-to-2010 periods.

Для цитирования: Wang Xiaohong Iris, Thomas Jaiyeola, Zhang Songlin. Changing trends in human papillomavirus-associated head and neck squamous cell carcinoma.. Annals of diagnostic pathology. 2011. DOI: 10.1016/j.anndiagpath.2011.07.003.

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