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Combination of p16 INK4a /Ki67 immunocytology and hpv polymerase chain reaction for the noninvasive analysis of HPV involvement in head and neck cancer
Author(s) -
Linxweiler Maximilian,
Bochen Florian,
Wemmert Silke,
Lerner Cornelia,
Hasenfus Andrea,
Bohle Rainer Maria,
AlKadah Basel,
Takacs Zoltan Ferenc,
Smola Sigrun,
Schick Bernhard
Publication year - 2015
Publication title -
cancer cytopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.29
H-Index - 57
eISSN - 1934-6638
pISSN - 1934-662X
DOI - 10.1002/cncy.21512
Subject(s) - polymerase chain reaction , medicine , papanicolaou stain , pathology , cancer , staining , head and neck cancer , head and neck squamous cell carcinoma , hpv infection , biomarker , cancer research , cervical cancer , biology , gene , biochemistry
BACKGROUND High‐risk human papillomavirus (HPV) infection has been identified as a relevant risk for the development of head and neck squamous cell carcinomas (HNSCCs). As HPV status has also gained a role as a prognostic and predictive biomarker for this entity, there is a growing demand for valid HPV testing in HNSCC patients METHODS Liquid‐based cytological smears from 45 HNSCC and 20 control patients were collected and used for simultaneous immunocytochemical p16 INK4a /Ki67 staining using a CINtec PLUS kit after the presence of tumor cells was verified in a Papanicolaou‐stained slide. The same cytological suspension was used for the detection of HPV DNA by specific polymerase chain reaction (PCR). RESULTS Tumor cells were detected in the swab material of 44 HNSCC patients corresponding to a sensitivity of 98% (44 of 45). PCR analysis revealed the presence of HPV DNA in the cytological suspension of 13 patients (13 of 65, 20%) with simultaneous p16 INK4a /Ki67 expression by the tumor cells in 11 of these HPV DNA–positive samples (11 of 13, 85%) — a staining pattern that is strongly associated with a carcinogenic HPV infection. CONCLUSIONS A simultaneous immunocytochemical detection of p16 INK4a and Ki67 can reliably be performed on liquid‐based cytological smears from HNSCC patients using a CINtec PLUS kit. In addition, the same cytological material can be used for the detection of HPV DNA by specific PCR. The combined results of both techniques enable better discrimination between latent and carcinogenic HPV infections as well as HPV‐negative cases and thus can provide information on the prognosis of HNSCC patients and facilitate therapeutic decisions. Cancer (Cancer Cytopathol) 2015;123:219–229. © 2014 American Cancer Society.