Oral HPV16 DNA as a screening tool to detect early oropharyngeal squamous cell carcinoma

被引:26
|
作者
Tang, Kai D. [1 ,2 ]
Vasani, Sarju [3 ]
Menezes, Lilian [1 ]
Taheri, Touraj [4 ,5 ]
Walsh, Laurence J. [6 ]
Hughes, Brett G. M. [5 ,7 ]
Frazer, Ian H. [8 ]
Kenny, Liz [5 ,7 ,9 ]
Scheper, Gert C. [10 ]
Punyadeera, Chamindie [1 ,2 ]
机构
[1] Queensland Univ Technol, Sch Biomed Sci, Inst Hlth & Biomed Innovat, Sal & Liquid Biopsy Translat Lab, 60 Musk Ave,GPO Box 2434, Brisbane, Qld 4059, Australia
[2] Translat Res Inst, Woolloongabba, Qld, Australia
[3] Royal Brisbane & Womens Hosp, Dept Otolaryngol, Herston, Qld, Australia
[4] Royal Brisbane & Womens Hosp, Dept Anat Pathol, Herston, Qld, Australia
[5] Univ Queensland, Sch Med, St Lucia, Qld, Australia
[6] Univ Queensland, Sch Dent, St Lucia, Qld, Australia
[7] Royal Brisbane & Womens Hosp, Dept Canc Care Serv, Herston, Qld, Australia
[8] Univ Queensland, Fac Med, Translat Res Inst, Brisbane, Qld, Australia
[9] Queensland Hlth, Cent Integrated Reg Canc Serv, Brisbane, Qld, Australia
[10] Janssen Vaccines & Prevent BV, Leiden, Netherlands
关键词
biomarkers; human papillomavirus; oropharyngeal squamous cell carcinoma; saliva; screening tools; HUMAN-PAPILLOMAVIRUS TYPE-16; LONG-TERM PERSISTENCE; NATURAL-HISTORY; HEAD; INFECTION; CANCER; RISK; PREVALENCE; SALIVA; VACCINATION;
D O I
10.1111/cas.14585
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Given that oropharyngeal squamous cell carcinoma (OPSCC) have now surpassed cervical cancer as the most common human papillomavirus (HPV)-driven cancer, there is an interest in developing non-invasive predictive biomarkers to early detect HPV-driven OPSCC. In total, 665 cancer-free individuals were recruited from Queensland, Australia. Oral HPV16 DNA positivity in those individuals was determined by our in-house developed sensitive PCR method. Individuals with (n = 9) or without (n = 12) oral HPV16 infections at baseline were followed for a median duration of 24 mo. Individuals with persistent oral HPV16 infection (>= 30 mo) were invited for clinical examination of their oral cavity and oropharynx by an otolaryngologist. Oral HPV16 DNA was detected in 12 out of 650 cancer-free individuals (1.8%; 95% confidence interval [CI]: 1.0-3.2). Of the 3 individuals with persistent oral HPV16 infection, the first individual showed no clinical evidence of pathology. The second individual was diagnosed with a 2 mm invasive squamous cell carcinoma (T1N0M0) positive for both p16INK4a expression and HPV16 DNA. The third individual was found to have a mildly dysplastic lesion in the tonsillar region that was negative for p16INK4a expression and HPV16 DNA and she continues to have HPV16 DNA in her saliva. Taken together, our data support the value of using an oral HPV16 DNA assay as a potential screening tool for the detection of microscopic HPV-driven OPSCC. Larger multicenter studies across various geographic regions recruiting populations at a higher risk of developing HPV-driven OPSCC are warranted to extend and confirm the results of the current investigation.
引用
收藏
页码:3854 / 3861
页数:8
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