Journal of Otolaryngology-Head & Neck Surgery | |
HPV Status and second primary tumours in Oropharyngeal Squamous Cell Carcinoma | |
Hadi Seikaly1  Lakshmi Puttagunta2  Vincent L Biron1  Caroline C Xu1  | |
[1] Division of Otolaryngology-Head and Neck Surgery, Department of Surgery, University of Alberta Hospital, 8440 112 St, Edmonton, AB T6H 2H7, Canada;Department of Laboratory Medicine and Pathology, University of Alberta Hospital, 8440 112 St, Edmonton, AB, T6H 2H7, Canada | |
关键词: P16; HPV; Panendoscopy; Second primary tumours; Oropharynx; | |
Others : 861748 DOI : 10.1186/1916-0216-42-36 |
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received in 2013-01-08, accepted in 2013-04-01, 发布年份 2013 | |
【 摘 要 】
Introductions
The incidence of human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCCs) is rising in developed nations. Studies have shown that these virally mediated tumours are epidemiologically, clinically, and biologically different than other head and neck squamous cell carcinomas and traditional concepts of field cancerization may not apply to HPV-related oropharyngeal cancer.
Objective
The purpose of this study was to evaluate the rate of second primary tumors and the diagnostic yield of field cancerization work up in the upper aerodigestive tract in patients with HPV-related and HPV-unrelated oropharyngeal squamous cell carcinoma.
Design
Retrospective review.
Setting
Tertiary cancer care centers in Alberta.
Methods
Retrospective review of 406 patients diagnosed with OPSCC in Alberta between 2005 and 2009. HPV-status of tumours was determined by tissue microarray using immunohistochemistry staining for p16.
Main outcome measures
Primary outcome: incidence of upper aerodigestive tract second primary tumours in p16-positive versus p16-negative OPSCC. Secondary outcomes: diagnostic yield of traditional field cancerization work-up in p16-positive versus negative patients.
Results
The overall rate of SPTs was 7.4% (30/406). The incidence rate of SPTs was significantly lower in p16-positive patients (0.7 per 100 patient-yrs vs. 8.5 in p16-negative, p < 0.0001). Field cancerization work-up for synchronous lesions in the upper aerodigestive tract, including panendoscopy and whole-body PET-CT, had decreased diagnostic yield in p16-positive patients (2.8% vs. 10.2% in HPV-negative patients, p=0.02).
Conclusions
Patients with HPV-related OPSCC, who are non-smokers have decreased risk of developing second primary tumours in the upper aerodigestive tract and have low yield on field cancerization work-up. This study provides further evidence that virally mediated OPSCC are distinct and may benefit from alternate diagnostic pathways.
【 授权许可】
2013 Xu et al.; licensee BioMed Central Ltd.
【 预 览 】
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【 参考文献 】
- [1]Johnson-Obaseki S, McDonald JT, Corsten M, Rourke R: Head and Neck Cancer in Canada: Trends 1992 to 2007. Otolaryngol Head Neck Surg 2012, 147(1):74-78. Epub Feb 10
- [2]Ryerson AB, Peters ES, Coughlin SS, Chen VW, Gillison ML, Reichman ME, Wu X, Chaturvedi AK, Kawaoka K: Burden of potentially human papillomavirus-associated cancers of the oropharynx and oral cavity in the US, 1998–2003. Cancer 2008 Nov 15, 113(10 Suppl):2901-2909.
- [3]Heath S, Willis V, Allan K, Purdie K, Harwood C, Shields P, Simcock R, Williams T, Gilbert DC: Clinically significant human papilloma virus in squamous cell carcinoma of the head and neck in UK practice. Clin Oncol (R Coll Radiol) 2012, 24(1):e18-e23. Epub 2011 Jul 14
- [4]van Monsjou HS, Balm AJ, van den Brekel MM, Wreesmann VB: Oropharyngeal squamous cell carcinoma: a unique disease on the rise? Oral Oncol 2010, 46(11):780-785. Review
- [5]McKaig RG, Baric RS, Olshan AF: Human papitlonia- virus and head and neck cancer: epidemiology and molecular biology. Head Neck 1998, 20:250-265.
- [6]Van Houten VM, Snijders PJ, Van den Brckel MW, Kummer JA: Biological evidence that human papillomaviruses are etiologically involved in a subgroup of head and neck squamous cell carcinomas. Int J Cancer 2001, 93:232-235.
- [7]Fouret P, Monceaux G, Temam S: Human papillomavirus in head and neck squamous cell carcinomas in nonsmokers. Arch Otolaryngol Head Neck Surg 1997, 123:513-516.
- [8]Biron VL, Côté DW, Seikaly H: Oropharyngeal squamous cell carcinoma and human papillomavirus-associated cancers in women: epidemiologic evaluation of association. J Otolaryngol Head Neck Surg 2011 Feb, 40(Suppl 1):S65-S69.
- [9]Gillison ML, D’Souza G, Westra W: Distinct risk factor profiles for human papillomavirus type 16-positive and human papillomavirus type 16-negative head and neck cancers. J Natl Cancer Inst 2008, 100:407-420.
- [10]Ang KK, Harris J, Wheeler R: Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med 2010, 363:24-35.
- [11]Leemans CR, Braakhuis BJM, Brakenhoff RH: The molecular biology of head and neck cancer. Nat Rev Cancer 2011, 11:9-22.
- [12]Levine B, Nielsen EW: The justifications and controversies of panendoscopy - A review. Ear, Nose and Throat J 1992, 71(8):335-343.
- [13]Xu GX, Guan DJ, He ZY: 18FDG-PET/CT for detecting distant metastases and second primary cancers in patients with head and neck cancer: a metanalysis. Oral Oncology 2011, 47(7):560-565.
- [14]D'Souza G, Kreimer AR, Viscidi R: Case–control study of human papillomavirus and oropharyngeal cancer. N Engl J Med 2007, 356:1944-1956.
- [15]Licitra L, Perrone F, Bossi P: High-risk human papillomavirus affects prognosis in patients with surgically treated oropharyngeal squamous cell carcinoma. J Clin Oncol 2006, 24:5630-5636.
- [16]Morris LGT, Sikora AG, Patel SG: Second primary cancers after an index head and neck cancer : subsite-specific trends in the era of human papillomavirus – associated oropharygneal cancer. J of Clin Onc 2011, 29(6):739-746.
- [17]Kononen J, Bubendorf L, Kallioniemi A: Tissue microarrays for high-throughput molecular profiling of tumor specimens. Nat Med 1998, 4:844-847.
- [18]Prabhu PR, Jayalekshmi D, Pillai MR: Lung cancer and human papilloma viruses (HPVs): examining the molecular evidence. J Oncol 2012., 750270Epub 2012 Jan 26
- [19]Benninger MS, Shariff A, Blazoff K: Symptom-directed selective endoscopy: long-term efficacy. Arch Otolaryngol Head Neck Surg 2001, 127(7):770-3.
- [20]Kurien G, Hu J, Harris J, Seikaly H: Cost-effectiveness of positron emission tomography/computed tomography in the management of advanced head and neck cancer. J Otolaryngol Head Neck Surg 2011 Dec, 40(6):468-72.
- [21]Goyal P, Hsu JM, Kellman RM: Effect of 18F-fluorodeoxyglucose positron emission tomography on the management of patients with head and neck squamous cell carcinoma. J Otolaryngol Head Neck Surg 2008, 37:694-9.
- [22]Smith EM, Rubenstein LM, Haugen TH: Tobacco and alcohol use increases the risk of both HPV-associated and HPV-independent head and neck cancers. Cancer Causes Control 2010, 21:1369-78.
- [23]Pannone G, Rodolico V, Santoro A: Evaluation of combined triple method to detecet causative HPV in oral and oropharyngeal squamous cell carcinomas: p16 immunohistochemistry, consensus PCR HPV-DNA, and in situ hybridization. Infect Agent Cancer 2012, 7(1):4. BioMed Central Full Text