Multicentric human papillomavirus-associated head and neck squamous cell carcinoma

被引:11
|
作者
Caley, Andrew [1 ]
Evans, Mererid [1 ]
Powell, Ned [2 ]
Paleri, Vinidh [3 ]
Tomkinson, Alun [4 ]
Urbano, Teresa Guerrero [5 ]
Jay, Amrita [6 ]
Robinson, Max [7 ]
Thavaraj, Selvam [8 ]
机构
[1] Velindre Canc Ctr, Dept Clin Oncol, Cardiff, S Glam, Wales
[2] Cardiff Univ, HPV Res Grp, Sch Med, Cardiff CF10 3AX, S Glam, Wales
[3] Newcastle Univ, Dept Otolaryngol Head & Neck Surg, Newcastle Upon Tyne Hosp NHS Trust, Northern Inst Canc Res, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Univ Wales Hosp, Dept Otolaryngol Head & Neck Surg, Cardiff CF4 4XW, S Glam, Wales
[5] Guys & St Thomas NHS Fdn Trust, London, England
[6] Univ Coll London Hosp, Dept Histopathol, London, England
[7] Newcastle Univ, Ctr Oral Hlth Res, Sch Dent Sci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[8] Kings Coll London Dent Inst, London, England
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2015年 / 37卷 / 02期
基金
英国医学研究理事会;
关键词
second primary tumor; human papillomavirus; head and neck squamous cell carcinoma; multicentric; pharyngeal; RISK HUMAN-PAPILLOMAVIRUS; LOWER GENITAL-TRACT; OROPHARYNGEAL CANCER INCIDENCE; 2ND PRIMARY TUMORS; TONSILLAR CARCINOMA; UNITED-STATES; HPV; SURVIVAL; EPIDEMIC; TRENDS;
D O I
10.1002/hed.23584
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
BackgroundThe purpose of this study was to present the clinicopathological features of a series of patients with human papillomavirus (HPV)-associated head and neck second primary tumors. MethodsPatients with HPV-associated head and neck second primary tumors from 3 centers were identified. HPV infection was evaluated using p16 by immunohistochemistry (IHC), high-risk HPV DNA by in situ hybridization (ISH), and HPV genotyping by DNA polymerase chain reaction (PCR) enzyme immunoassay (EIA). ResultsEleven patients were identified: 5 with synchronous and 6 with metachronous HPV-positive second primary tumors, the latter demonstrating a mean time interval of 5 years. There were 13 second primary tumors: 11 oropharyngeal, 1 nasopharyngeal, and 1 floor of the mouth. Nine of 10 genotyped patients harbored HPV-16, and 1 patient had HPV-33 in 3 synchronous tumors. ConclusionHPV-associated second primary tumors may present as synchronous and/or metachronous lesions and can arise outside the oropharynx after prolonged intervals. Further work is necessary to identify patients at risk and to elucidate the mechanisms of HPV-associated head and neck second primary tumors. (c) 2014 Wiley Periodicals, Inc. Head Neck37: 202-208, 2015
引用
收藏
页码:202 / 208
页数:7
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