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HPV-associated head and neck squamous cell carcinoma
Monday 26 March 2012
HPV-positive oropharyngeal cancer; HPV-related head and neck squamous cell carcinoma; HPV-associated HNSCC; HPV-HNSCC
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Definition: Human papilloma virus (HPV)-related squamous cell carcinoma is a distinct variant of head and neck squamous cell carcinoma (HNSCC).
Human papilloma virus (HPV)-related oropharyngeal carcinoma represents a clinically distinct form of head and neck squamous cell carcinoma (HNSCC) that results from oral HPV infection. These tumors are associated with an improved overall survival, progression-free survival, and disease-specific survival in comparison to their HPV-negative counterparts.
Epidemiology
In contrast to HPV-negative HNSCC, which has been gradually decreasing in incidence in the United States due to a decline in tobacco exposure, HPV-related HNSCC has seen a dramatic increase in overall incidence (225% from 1998 to 2004 / 6 years).
HPV-related HNSCC is typically seen in younger patients (@<@60 years) whose sexual behavior increases risk factors for HPV infection including early age of sexual contact, high number of lifetime sexual partners, oral–genital and oral–anal sex, and lack of barrier protection during sexual contact.
HPV-related HNSCC has a strong association with oral high-risk HPV (HR-HPV) infection, most frequently HPV type 16 (85–90% of cases).
These tumors are more frequently encountered in men than in women who are often non-smokers and without a history of alcohol abuse.
They most commonly involve the oropharynx, with particular predilection for the tonsil and base of the tongue.
Physiopathology
HPV-related HNSCC is driven by the production of viral oncoproteins E6 and E7, which interfere with the p53 and retinoblastoma (Rb) tumor suppressor pathways.
Inactivation of Rb by E7 leads to upregulation and overexpression of p16. Immunohistochemical (IHC) detection of p16 in tumor cells is thus often used as a surrogate for HR-HPV infection.
Prognostic
HPV-related HNSCC forms a distinct clinicopathologic entity primarily because of its much improved prognosis and clinical outcomes when compared with non-HPV associated HNSCC.
The option of treating these patients with less intense chemo/radiotherapy than conventional treatment for non-HPV HNSCC is currently being addressed in clinical trials.
Microscopy
The most common histomorphology seen in HPV-related HNSCC is a non-keratinizing basaloid form of squamous cell carcinoma (SCC). This tumor typically infiltrates in sheets, cords, and lobules with associated central necrosis often leading to cystic degeneration.
Strong stromal desmoplastic response is uncommon, but hyalinization is usual, and the tumor is often surrounded by lymphoid tissue which may infiltrate as tumor-infiltrating lymphocytes (TILs) thereby imparting a lymphoepithelial-like appearance.
Cytologically, malignant cells display high nuclear–cytoplasmic ratios giving a classic basaloid appearance. Cytoplasmic keratinization and intercellular bridges are absent.
The distinction of HPV-related HNSCC with basaloid cytomorphology from clinically aggressive non-HPV-related basaloid variant of HNSCC is important.
Other morphologic variants of HPV-related HNSCCs reported in the literature include papillary, adenosquamous, ciliated and rare reports of small cell transformation which is associated with a more aggressive behavior and poor prognosis.
HPV-related HNSCCs frequently undergo necrosis and cystic degeneration, especially when they metastasize to cervical lymph nodes resulting in cystic degeneration.
The cystic change in an enlarged cervical node with a metastatic deposit is so characteristic of HPV-related HNSCC that in the absence of a known primary, an occult oropharyngeal HPV-related HNSCC should always be suspected.
Oropharyngeal HNSCCs frequently present with small, often occult tumors, and low tumor (T) stage disease but with higher nodal (N) stage and enlarged metastatic cervical lymph nodes.
Cytology
The role of cytology for the diagnosis of HPV-related HNSCC at the primary site is very limited.
The small size of the tumors, together with the most prevalent sites of occurrence in the base of tongue and tonsillar crypts, makes cytological sampling techniques such as oral brushing/rinsing relatively ineffective for detection of these tumors.
Therefore, an oral Papanicolaou (Pap) screening test similar to the hugely successful cervical cytology screening has not been considered for early diagnosis of HPV-related HNSCC.
In contrast to the limited role of traditional cytology for the diagnosis of HPV-related HNSCC in the oropharynx, fine-needle aspiration (FNA) biopsy of enlarged metastatic neck lymph nodes very often plays a significant role in the initial diagnosis of HPV-related HNSCC.
The role of neck lymph node FNA in the recognition of occult HPV-related HNSCC in patients who present with metastatic carcinoma of unknown primary is now well accepted clinically.
Therefore, evaluating HPV status in any patient with a newly diagnosed metastatic SCC to a neck node without a known primary is highly recommended in determining a primary site of origin. Having a positive HPV result is a strong indicator of oropharyngeal origin and facilitates clinical management.
FNA biopsy results in these patients lead to targeted endoscopic examination of the oropharynx, particularly the tongue base and tonsils, to identify the primary tumor site.
In the rare event of an unidentified primary site despite exhaustive clinical/radiological evaluation, positive HPV status can be used to direct localized radiation therapy to the oropharynx instead of irradiating the entire upper respiratory mucosa, thereby sparing the patient significant morbidity and associated complications.
The possibility of metastatic HPV-related squamous cell carcinoma (SCC) from distant sites such as lung and cervix needs to be excluded in such patients because of the significant morphologic and immunophenotypic overlap in SCCs arising from different sites.
Staging
ICON-S staging system (26936027)
metastasis
- metastatic HPV-associated HNSCC
Open References
Human Papillomavirus Testing in Head and Neck Carcinomas. 2017. doi : 10.5858/arpa.2017-0286-CP
References
Development and validation of a staging system for HPV-related oropharyngeal cancer by the International Collaboration on Oropharyngeal cancer Network for Staging (ICON-S): a multicentre cohort study. O’Sullivan B, Huang SH, Su J, Garden AS, Sturgis EM, Dahlstrom K, Lee N, Riaz N, Pei X, Koyfman SA, Adelstein D, Burkey BB, Friborg J, Kristensen CA, Gothelf AB, Hoebers F, Kremer B, Speel EJ, Bowles DW, Raben D, Karam SD, Yu E, Xu W. Lancet Oncol. 2016 Feb 26. pii: S1470-2045(15)00560-4. doi : 10.1016/S1470-2045(15)00560-4 PMID: 26936027
Chaturvedi, A.K., Engels, E.A., Anderson, W.F. et al. Incidence trends for human papillomavirus-related and unrelated oral squamous cell carcinomas in the United States. J Clin Oncol. 2008; 26: 612–619. 24625808
Chaturvedi, A.K., Engels, E.A., Pfeiffer, R.M. et al. Human papillomavirus and rising oropharyngeal cancer incidence in the United States. J Clin Oncol. 2011; 29: 4294–4301.
Chaturvedi, A.K., Graubard, B.I., Pickard, R.K. et al. High-risk oral human papillomavirus load in the US population, National Health and Nutrition Examination Survey 2009–2010. J Infect Dis. 2014; 210: 441–447. 24625808
Smith, E.M., Ritchie, J.M., Summersgill, K.F. et al. Age, sexual behavior and human papillomavirus infection in oral cavity and oropharyngeal cancers. Int J Cancer. 2004; 108: 766–772
Summersgill, K.F., Smith, E.M., Levy, B.T. et al. Human papillomavirus in the oral cavities of children and adolescents. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001; 91: 62–69
Kreimer, A.R., Alberg, A.J., Daniel, R. et al. Oral human papillomavirus infection in adults is associated with sexual behavior and HIV serostatus. J Infect Dis. 2004; 189: 686–698
Kreimer, A.R., Alberg, A.J., Viscidi, R. et al. Gender differences in sexual biomarkers and behaviors associated with human papillomavirus-16, -18, and -33 seroprevalence. Sex Transm Dis. 2004; 31: 247–256
Marur, S., D’Souza, G., Westra, W.H. et al. HPV-associated head and neck cancer: a virus-related cancer epidemic. Lancet Oncol. 2010; 11: 781–789
HPV analysis
HPV analysis in distinguishing second primary tumors from lung metastases in patients with head and neck squamous cell carcinoma. Bishop JA, Ogawa T, Chang X, Illei PB, Gabrielson E, Pai SI, Westra WH. Am J Surg Pathol. 2012 Jan;36(1):142-8. PMID: 22173119
Chaturvedi, A.K., Engels, E.A., Anderson, W.F. et al. Incidence trends for human papillomavirus-related and unrelated oral squamous cell carcinomas in the United States. J Clin Oncol. 2008; 26: 612–619
Chaturvedi, A.K., Engels, E.A., Pfeiffer, R.M. et al. Human papillomavirus and rising oropharyngeal cancer incidence in the United States. J Clin Oncol. 2011; 29: 4294–4301
Gillison, M.L., Koch, W.M., Capone, R.B. et al. Evidence for a causal association between human papillomavirus and a subset of head and neck cancers. J Natl Cancer Inst. 2000; 92: 709–720
Sturgis, E.M. and Cinciripini, P.M. Trends in head and neck cancer incidence in relation to smoking prevalence: an emerging epidemic of human papillomavirus-associated cancers?. Cancer. 2007; 110: 1429–1435
Paz, I.B., Cook, N., Odom-Maryon, T. et al. Human papillomavirus (HPV) in head and neck cancer. An association of HPV 16 with squamous cell carcinoma of Waldeyer’s tonsillar ring. Cancer. 1997; 79: 595–604
Hammarstedt, L., Lindquist, D., Dahlstrand, H. et al. Human papillomavirus as a risk factor for the increase in incidence of tonsillar cancer. Int J Cancer. 2006; 119: 2620–2623
Ang, K.K., Harris, J., Wheeler, R. et al. Human papillomavirus and survival of patients with oropharyngeal cancer. N Engl J Med. 2010; 363: 24–35
Fakhry, C., Westra, W.H., Li, S. et al. Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial. J Natl Cancer Inst. 2008; 100: 261–269
O’Rorke, M.A., Ellison, M.V., Murray, L.J. et al. Human papillomavirus related head and neck cancer survival: a systematic review and meta-analysis. Oral Oncol. 2012; 48: 1191–1201
Bonilla-Velez, J., Mroz, E.A., Hammon, R.J. et al. Impact of human papillomavirus on oropharyngeal cancer biology and response to therapy: implications for treatment. Otolaryngol Clin North Am. 2013; 46: 521–543
Chaturvedi, A.K., Graubard, B.I., Pickard, R.K. et al. High-risk oral human papillomavirus load in the US population, National Health and Nutrition Examination Survey 2009–2010. J Infect Dis. 2014; 210: 441–447
Smith, E.M., Ritchie, J.M., Summersgill, K.F. et al. Age, sexual behavior and human papillomavirus infection in oral cavity and oropharyngeal cancers. Int J Cancer. 2004; 108: 766–772
Summersgill, K.F., Smith, E.M., Levy, B.T. et al. Human papillomavirus in the oral cavities of children and adolescents. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2001; 91: 62–69
Kreimer, A.R., Alberg, A.J., Daniel, R. et al. Oral human papillomavirus infection in adults is associated with sexual behavior and HIV serostatus. J Infect Dis. 2004; 189: 686–698
Kreimer, A.R., Alberg, A.J., Viscidi, R. et al. Gender differences in sexual biomarkers and behaviors associated with human papillomavirus-16, -18, and -33 seroprevalence. Sex Transm Dis. 2004; 31: 247–256
Begum, S., Cao, D., Gillison, M. et al. Tissue distribution of human papillomavirus 16 DNA integration in patients with tonsillar carcinoma. Clin Cancer Res. 2005; 11: 5694–5699
Gillison, M.L., D’Souza, G., Westra, W. et al. 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
Vidal, L. and Gillison, M.L. Human papillomavirus in HNSCC: recognition of a distinct disease type. Hematol Oncol Clin North Am. 2008; 22: 1125–1142
Marur, S., D’Souza, G., Westra, W.H. et al. HPV-associated head and neck cancer: a virus-related cancer epidemic. Lancet Oncol. 2010; 11: 781–789
Cohan, D.M., Popat, S., Kaplan, S.E. et al. Oropharyngeal cancer: current understanding and management. Curr Opin Otolaryngol Head Neck Surg. 2009; 17: 88–94
Wiest, T., Schwarz, E., Enders, C. et al. Involvement of intact HPV16 E6/E7 gene expression in head and neck cancers with unaltered p53 status and perturbed pRb cell cycle control. Oncogene. 2002; 21: 1510–1517
Andl, T., Kahn, T., Pfuhl, A. et al. Etiological involvement of oncogenic human papillomavirus in tonsillar squamous cell carcinomas lacking retinoblastoma cell cycle control. Cancer Res. 1998; 58: 5–13
Strati, K. and Lambert, P.F. Role of Rb-dependent and Rb-independent functions of papillomavirus E7 oncogene in head and neck cancer. Cancer Res. 2007; 67: 11585–11593
Singhi, A.D. and Westra, W.H. Comparison of human papillomavirus in situ hybridization and p16 immunohistochemistry in the detection of human papillomavirus-associated head and neck cancer based on a prospective clinical experience. Cancer. 2010; 116: 2166–2173
El-Naggar, A.K. and Westra, W.H. p16 Expression as a surrogate marker for HPV-related oropharyngeal carcinoma: a guide for interpretative relevance and consistency. Head Neck. 2012; 34: 459–461
Chung, C.H. and Schwartz, D.L. Impact of HPV-related head and neck cancer in clinical trials: opportunity to translate scientific insight into personalized care. Otolaryngol Clin North Am. 2012; 45: 795–806
Pai, S.I. and Westra, W.H. Molecular pathology of head and neck cancer: implications for diagnosis, prognosis, and treatment. Annu Rev Pathol. 2009; 4: 49–70
Chernock, R.D., El-Mofty, S.K., Thorstad, W.L. et al. HPV-related nonkeratinizing squamous cell carcinoma of the oropharynx: utility of microscopic features in predicting patient outcome. Head Neck Pathol. 2009; 3: 186–194
Westra, W.H. The changing face of head and neck cancer in the 21st century: the impact of HPV on the epidemiology and pathology of oral cancer. Head Neck Pathol. 2009; 3: 78–81
El-Mofty, S.K. and Lu, D.W. Prevalence of human papillomavirus type 16 DNA in squamous cell carcinoma of the palatine tonsil, and not the oral cavity, in young patients: a distinct clinicopathologic and molecular disease entity. Am J Surg Pathol. 2003; 27: 1463–1470
Singhi, A.D., Stelow, E.B., Mills, S.E. et al. Lymphoepithelial-like carcinoma of the oropharynx: a morphologic variant of HPV-related head and neck carcinoma. Am J Surg Pathol. 2010; 34: 800–805
Begum, S. and Westra, W.H. Basaloid squamous cell carcinoma of the head and neck is a mixed variant that can be further resolved by HPV status. Am J Surg Pathol. 2008; 32: 1044–1050
Chernock, R.D., Lewis, J.S. Jr., Zhang, Q. et al. Human papillomavirus-positive basaloid squamous cell carcinomas of the upper aerodigestive tract: a distinct clinicopathologic and molecular subtype of basaloid squamous cell carcinoma. Hum Pathol. 2010; 41: 1016–1023
Jo, V.Y., Mills, S.E., Stoler, M.H. et al. Papillary squamous cell carcinoma of the head and neck: frequent association with human papillomavirus infection and invasive carcinoma. Am J Surg Pathol. 2009; 33: 1720–1724
Masand, R.P., El-Mofty, S.K., Ma, X.J. et al. Adenosquamous carcinoma of the head and neck: relationship to human papillomavirus and review of the literature. Head Neck Pathol. 2011; 5: 108–116
Bishop, J.A. and Westra, W.H. Human papillomavirus-related small cell carcinoma of the oropharynx. Am J Surg Pathol. 2011; 35: 1679–1684
Kraft, M., Simmen, D., Casas, R. et al. Significance of human papillomavirus in sinonasal papillomas. J Laryngol Otol. 2001; 115: 709–714
Goldenberg, D., Begum, S., Westra, W.H. et al. Cystic lymph node metastasis in patients with head and neck cancer: an HPV-associated phenomenon. Head Neck. 2008; 30: 898–903
Begum, S., Gillison, M.L., Ansari-Lari, M.A. et al. Detection of human papillomavirus in cervical lymph nodes: a highly effective strategy for localizing site of tumor origin. Clin Cancer Res. 2003; 9: 6469–6475
Begum, S., Gillison, M.L., Nicol, T.L. et al. Detection of human papillomavirus-16 in fine-needle aspirates to determine tumor origin in patients with metastatic squamous cell carcinoma of the head and neck. Clin Cancer Res. 2007; 13: 1186–1191
El-Mofty, S.K., Zhang, M.Q., and Davila, R.M. Histologic identification of human papillomavirus (HPV)-related squamous cell carcinoma in cervical lymph nodes: a reliable predictor of the site of an occult head and neck primary carcinoma. Head Neck Pathol. 2008; 2: 163–168
Thompson, H.Y., Fulmer, R.P., and Schnadig, V.J. Metastatic squamous cell carcinoma of the tonsil presenting as multiple cystic neck masses. Report of a case with fine needle aspiration findings. Acta Cytol. 1994; 38: 605–607
Thompson, L.D. Metastatic cystic squamous cell carcinoma. Ear Nose Throat J. 2005; 84: 272–273
Thompson, L.D. and Heffner, D.K. The clinical importance of cystic squamous cell carcinomas in the neck: a study of 136 cases. Cancer. 1998; 82: 944–956
Lingen, M.W. Brush-based cytology screening in the tonsils and cervix: there is a difference!. Cancer Prev Res (Phila). 2011; 4: 1350–1352
Jarboe, E.A., Willis, M., Bentz, B. et al. Detection of human papillomavirus using Hybrid Capture 2 in oral brushings from patients with oropharyngeal squamous cell carcinoma. Am J Clin Pathol. 2011; 135: 766–769
Fakhry, C., Rosenthal, B.T., Clark, D.P. et al. Associations between oral HPV16 infection and cytopathology: evaluation of an oropharyngeal “pap-test equivalent” in high-risk populations. Cancer Prev Res (Phila). 2011; 4: 1378–1384
de Braud, F. and al-Sarraf, M. Diagnosis and management of squamous cell carcinoma of unknown primary tumor site of the neck. Semin Oncol. 1993; 20: 273–278
Bishop, J.A., Ogawa, T., Chang, X. et al. HPV analysis in distinguishing second primary tumors from lung metastases in patients with head and neck squamous cell carcinoma. Am J Surg Pathol. 2012; 36: 142–148
Weichert, W., Schewe, C., Denkert, C. et al. Molecular HPV typing as a diagnostic tool to discriminate primary from metastatic squamous cell carcinoma of the lung. Am J Surg Pathol. 2009; 33: 513–520
Jarboe, E.A., Hunt, J.P., and Layfield, L.J. Cytomorphologic diagnosis and HPV testing of metastatic and primary oropharyngeal squamous cell carcinomas: a review and summary of the literature. Diagn Cytopathol. 2012; 40: 491–497
Cao, D., Begum, S., Ali, S.Z. et al. Expression of p16 in benign and malignant cystic squamous lesions of the neck. Hum Pathol. 2010; 41: 535–539
Pai, R.K., Erickson, J., Pourmand, N. et al. p16(INK4A) immunohistochemical staining may be helpful in distinguishing branchial cleft cysts from cystic squamous cell carcinomas originating in the oropharynx. Cancer. 2009; 117: 108–119
Banks, E.R., Frierson, H.F. Jr., and Covell, J.L. Fine needle aspiration cytologic findings in metastatic basaloid squamous cell carcinoma of the head and neck. Acta Cytol. 1992; 36: 126–131
Marks, R.A., Cramer, H.M., and Wu, H.H. Fine-needle aspiration cytology of basaloid squamous cell carcinoma and small cell carcinoma-a comparison study. Diagn Cytopathol. 2013; 41: 81–84
Gilcrease, M.Z. and Guzman-Paz, M. Fine-needle aspiration of basaloid squamous carcinoma: a case report with review of differential diagnostic considerations. Diagn Cytopathol. 1998; 19: 210–215
Serrano, M.F., El-Mofty, S.K., Gnepp, D.R. et al. Utility of high molecular weight cytokeratins, but not p63, in the differential diagnosis of neuroendocrine and basaloid carcinomas of the head and neck. Hum Pathol. 2008; 39: 591–598
Chapman-Fredricks, J., Jorda, M., and Gomez-Fernandez, C. A limited immunohistochemical panel helps differentiate small cell epithelial malignancies of the sinonasal cavity and nasopharynx. Appl Immunohistochem Mol Morphol. 2009; 17: 207–210
Morice, W.G. and Ferreiro, J.A. Distinction of basaloid squamous cell carcinoma from adenoid cystic and small cell undifferentiated carcinoma by immunohistochemistry. Hum Pathol. 1998; 29: 609–612
Boland, J.M., McPhail, E.D., Garcia, J.J. et al. Detection of human papilloma virus and p16 expression in high-grade adenoid cystic carcinoma of the head and neck. Mod Pathol. 2012; 25: 529–536
Carpenter, D.H., El-Mofty, S.K., and Lewis, J.S. Jr. Undifferentiated carcinoma of the oropharynx: a human papillomavirus-associated tumor with a favorable prognosis. Mod Pathol. 2011; 24: 1306–1312
Dolcetti, R. and Menezes, J. Epstein–Barr virus and undifferentiated nasopharyngeal carcinoma: new immunobiological and molecular insights on a long-standing etiopathogenic association. Adv Cancer Res. 2003; 87: 127–157
Deyrup, A.T. Epstein–Barr virus-associated epithelial and mesenchymal neoplasms. Hum Pathol. 2008; 39: 473–483
Mohanty, S.K., Dey, P., Ghoshal, S. et al. Cytologic features of metastatic nasopharyngeal carcinoma. Diagn Cytopathol. 2002; 27: 340–342
Viguer, J.M., Jimenez-Heffernan, J.A., Lopez-Ferrer, P. et al. Fine-needle aspiration cytology of metastatic nasopharyngeal carcinoma. Diagn Cytopathol. 2005; 32: 233–237
Grenko, R.T. and Shabb, N.S. Metastatic nasopharyngeal carcinoma: cytologic features of 18 cases. Diagn Cytopathol. 1991; 7: 562–566
Jayaram, G., Swain, M., Khanijow, V. et al. Fine-needle aspiration cytology of metastatic nasopharyngeal carcinoma. Diagn Cytopathol. 1998; 19: 168–172
Holmes, B.J. and Westra, W.H. The expanding role of cytopathology in the diagnosis of HPV-related squamous cell carcinoma of the head and neck. Diagn Cytopathol. 2014; 42: 85–93
Krane, J.F. Role of cytology in the diagnosis and management of HPV-associated head and neck carcinoma. Acta Cytol. 2013; 57: 117–126
Faquin, W.C. Human papillomavirus (HPV) assays for testing fine-needle aspiration specimens in patients with head and neck squamous cell carcinoma. Cancer Cytopathol. 2014; 122: 92–95
Schlecht, N.F., Brandwein-Gensler, M., Nuovo, G.J. et al. A comparison of clinically utilized human papillomavirus detection methods in head and neck cancer. Mod Pathol. 2011; 24: 1295–1305
Lewis, J.S. Jr. p16 immunohistochemistry as a stand alone test for risk stratification in oropharyngeal squamous cell carcinoma. Head Neck Pathol. 2012; 6: S75–S82
Grimes, R., Garcia-Buitrago, M.T., Jorda, M. et al. p16INKa immunocytochemistry in fine-needle aspiration cytology smears of metastatic head and neck squamous cell carcinoma. Acta Cytol. 2013; 57: 33–37
Jakscha, J., Zlobec, I., Storck, C. et al. The clinical impact of p16 status in fine-needle aspirates of cervical lymph node metastasis of head and neck squamous cell carcinomas. Eur Arch Otorhinolaryngol. 2013; 270: 661–667
View in Article | CrossRef | PubMed | Scopus (1)
Jannapureddy, S., Cohen, C., Lau, S. et al. Assessing for primary oropharyngeal or nasopharyngeal squamous cell carcinoma from fine needle aspiration of cervical lymph node metastases. Diagn Cytopathol. 2010; 38: 795–800
Bishop, J.A., Ma, X.J., Wang, H. et al. Detection of transcriptionally active high-risk HPV in patients with head and neck squamous cell carcinoma as visualized by a novel E6/E7 mRNA in situ hybridization method. Am J Surg Pathol. 2012; 36: 1874–1882
Umudum, H., Rezanko, T., Dag, F. et al. Human papillomavirus genome detection by in situ hybridization in fine-needle aspirates of metastatic lesions from head and neck squamous cell carcinomas. Cancer. 2005; 105: 171–177
Zhang, M.Q., El-Mofty, S.K., and Davila, R.M. Detection of human papillomavirus-related squamous cell carcinoma cytologically and by in situ hybridization in fine-needle aspiration biopsies of cervical metastasis: a tool for identifying the site of an occult head and neck primary. Cancer. 2008; 114: 118–123
Hu, L., Guo, M., He, Z. et al. Human papillomavirus genotyping and p16INK4a expression in cervical intraepithelial neoplasia of adolescents. Mod Pathol. 2005; 18: 267–273
Schache, A.G., Liloglou, T., Risk, J.M. et al. Evaluation of human papilloma virus diagnostic testing in oropharyngeal squamous cell carcinoma: sensitivity, specificity, and prognostic discrimination. Clin Cancer Res. 2011; 17: 6262–6271
Lewis, J.S. Jr., Thorstad, W.L., Chernock, R.D. et al. p16 positive oropharyngeal squamous cell carcinoma: an entity with a favorable prognosis regardless of tumor HPV status. Am J Surg Pathol. 2010; 34: 1088–1096
Perrone, F., Gloghini, A., Cortelazzi, B. et al. Isolating p16-positive/HPV-negative oropharyngeal cancer: an effort worth making. Am J Surg Pathol. 2011; 35: 777–778
Bishop, J.A., Maleki, Z., Valsamakis, A. et al. Application of the Hybrid Capture 2 assay to squamous cell carcinomas of the head and neck: a convenient liquid-phase approach for the reliable determination of human papillomavirus status. Cancer Cytopathol. 2012; 120: 18–25
Smith, D.F., Maleki, Z., Coughlan, D. et al. Human papillomavirus status of head and neck cancer as determined in cytologic specimens using the hybrid-capture 2 assay. Oral Oncol. 2014; 50: 600–604
Solomides, C.C., Bibbo, M., and Wang, Z.X. Assessment of fine needle aspiration specimen adequacy for high-risk HPV detection and genotyping in oropharyngeal squamous cell carcinoma. Acta Cytol. 2012; 56: 196–198
Guo, M., Khanna, A., Dhillon, J. et al. Cervista HPV assays for fine-needle aspiration specimens are a valid option for human papillomavirus testing in patients with oropharyngeal carcinoma. Cancer Cytopathol. 2014; 122: 96–103
Kerr, D.A., Pitman, M.B., Sweeney, B. et al. Performance of the Roche cobas 4800 high-risk human papillomavirus test in cytologic preparations of squamous cell carcinoma of the head and neck. Cancer Cytopathol. 2014; 122: 167–174
Nishino, H.T., Tambouret, R.H., and Wilbur, D.C. Testing for human papillomavirus in cervical cancer screening: a review of indications and methodology. Cancer Cytopathol. 2011; 119: 219–227