2010
DOI: 10.1097/pas.0b013e3181e84652
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p16 Positive Oropharyngeal Squamous Cell Carcinoma:An Entity With a Favorable Prognosis Regardless of Tumor HPV Status

Abstract: Background In the human papillomavirus (HPV) era, the best way to assess oropharyngeal squamous carcinomas (SCC) for risk stratification is not clear. Many recommend use of both p16 immunohistochemistry and HPV in situ hybridization (ISH). A significant minority of tumors are p16 positive and HPV ISH negative, the significance of which is unclear. Methods Two hundred thirty-nine oropharyngeal SCC were tested by immunohistochemistry for p16 and by ISH for highrisk HPV. For p16 positive, HPV ISH negative cases… Show more

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Cited by 363 publications
(375 citation statements)
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References 35 publications
(66 reference statements)
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“…The HPV types have also been grouped into mucosal or cutaneous types, based on their tropism for specific epithelial sites. Mucosal HPV types found preferentially in precancerous and cancerous lesions have been designated as 'high-risk' types and these include types 16,18,31,33,34,35,39,45,51,52,56,58,59, 66, 68, and 70. Mucosal HPVs found in benign genital warts and other non-malignant lesions are generally labeled as 'low-risk' types, the most important ones being HPV 6,11,42,43, and 44 [1,2].…”
Section: Human Papillomaviruses (Structure and Classification)mentioning
confidence: 99%
See 1 more Smart Citation
“…The HPV types have also been grouped into mucosal or cutaneous types, based on their tropism for specific epithelial sites. Mucosal HPV types found preferentially in precancerous and cancerous lesions have been designated as 'high-risk' types and these include types 16,18,31,33,34,35,39,45,51,52,56,58,59, 66, 68, and 70. Mucosal HPVs found in benign genital warts and other non-malignant lesions are generally labeled as 'low-risk' types, the most important ones being HPV 6,11,42,43, and 44 [1,2].…”
Section: Human Papillomaviruses (Structure and Classification)mentioning
confidence: 99%
“…As was discussed earlier, not all viral genomes will replicate and in chronic infection replication can be activated every now and then. It has been suggested that the detection of E6 and E7 mRNAs would thus be the method of choice in HNSCC, together with p16 expression which is a surrogate marker for HPV [58]. However, one has to remember that p16 is also up-regulated in cellular senescence.…”
Section: Hpv and Head And Neck Cancer (Hnscc)mentioning
confidence: 99%
“…These tumors may present as different variants distinct from the typical keratinizingtype SCC, including nonkeratinizing [5,6], basaloid [7,8], and papillary SCC [9] and also undifferentiated carcinoma [10]. It has also been documented in several studies that HPV-related carcinomas of the upper aerodigestive tract have more favorable prognosis than HPV negative ones [11][12][13]. Most previous studies investigated HPV in tumors using DNA-based polymerase chain reaction (PCR) [14] while in more recent years DNA-based in situ hybridization (ISH) has been used [5,13,15].…”
Section: Introductionmentioning
confidence: 99%
“…Basaloid and warty morphologies are characteristic of HPV-associated squamous cell carcinomas and have been shown to correlate with viral status in oropharyngeal, 8 vulvar, 5 penile, 38 and anal carcinomas. 53 Bladder squamous cell carcinoma very rarely shows basaloid/warty features, which is consistent with the infrequent finding of HPV in bladder squamous cell carcinoma.…”
Section: Discussionmentioning
confidence: 99%
“…3,4 The oncogenic role of HPV is also well established for a subset of squamous cell carcinomas in the vulva, 5 penis, 6 anus, 7 and oropharynx. 8 The possible role of HPV infection in bladder tumors has not been completely elucidated as HPV detection rates vary widely from 0 to 100%, depending on the study. 9,10 An intriguing issue has been the possible association of the virus with bladder squamous cell carcinoma.…”
mentioning
confidence: 99%