Current status of clinical testing for human papillomavirus in oropharyngeal squamous cell carcinoma

被引:48
|
作者
Kim, Kelly Y. [1 ]
Lewis, James S., Jr. [2 ,3 ]
Chen, Zhong [4 ]
机构
[1] NCI, Canc Diag Program, Div Canc Treatment & Diag, NIH, Rockville, MD USA
[2] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA
[3] Vanderbilt Univ, Med Ctr, Dept Otolaryngol, Nashville, TN 37232 USA
[4] Natl Inst Deafness & Other Commun Disorders, Clin Genom Unit, Head & Neck Surg Branch, NIH, Bethesda, MD 20892 USA
来源
关键词
oropharyngeal cancer; oropharyngeal squamous cell carcinoma; OPSCC; head and neck cancer; human papillomavirus; HPV; p16; molecular diagnostics; biomarkers; RISK HUMAN-PAPILLOMAVIRUS; IN-SITU HYBRIDIZATION; ROCHE COBAS 4800; ADENOID CYSTIC CARCINOMA; ACTIVE HPV INFECTION; E6/E7; MESSENGER-RNA; NECK-CANCER; P16; IMMUNOHISTOCHEMISTRY; PATIENT OUTCOMES; HEAD;
D O I
10.1002/cjp2.111
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
While a variety of human papillomavirus (HPV) tests and surrogate markers are available, currently there is no consensus on the best detection method(s) that should be used to identify HPV-related oropharyngeal squamous cell carcinomas and serve as a standard test (or tests) for routine diagnostic use. As we begin to consider using the results of HPV testing for clinical purposes beyond simple prognostication, such as making decisions on treatment dose or duration or for targeted therapies that may be highly dependent on viral-mediated pathways, we need to be more rigorous in assessing and ensuring the performance of the test (or tests) used. Here we provide an overview of the platforms and technologies, including the strengths and limitations of each test, and discuss what steps are needed to generate confidence in their performance for use in clinical practice.
引用
收藏
页码:213 / 226
页数:14
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