The utility of high-risk human papillomavirus E6/E7 mRNA in situ hybridization in assessing HPV status on cell block.


Journal

Journal of the American Society of Cytopathology
ISSN: 2213-2945
Titre abrégé: J Am Soc Cytopathol
Pays: United States
ID NLM: 101613234

Informations de publication

Date de publication:
Historique:
received: 05 07 2020
revised: 17 09 2020
accepted: 17 09 2020
pubmed: 24 10 2020
medline: 7 1 2022
entrez: 23 10 2020
Statut: ppublish

Résumé

Assessment of human papillomavirus (HPV) status is critical to the treatment and prognosis of patients with oropharyngeal squamous cell carcinoma. Patients often present with enlarged cervical lymph nodes which are amenable to fine needle aspiration (FNA) and cell block creation. The most widely used method for assessing HPV status is the surrogate marker p16. Other HPV specific methods such as high-risk HPV E6/E7 mRNA in situ hybridization (ISH) have been shown to perform as well as p16 and are easier to interpret. Our study evaluates the utility of high-risk HPV mRNA ISH in cell block specimens. Thirty-six cases of metastatic squamous cell carcinoma in cervical neck lymph node FNAs were identified over a 3-year period. All cases had p16 immunohistochemistry (IHC) performed on cell block. HR HPV mRNA ISH was performed on the cell block and compared to the p16 results. Additionally, p16 and HR HPV mRNA ISH status was assessed in those cases with corresponding surgical resections. HR HPV mRNA ISH confirmed the p16 IHC (either positive or negative) in 24 of the 36 cases (66.7%). Six false negative cases were p16 negative/HR HPV mRNA ISH positive. HR HPV mRNA ISH was positive in 75% of the four p16 equivocal cases. Two cases were p16 positive/HR HPV mRNA ISH negative. HR HPV mRNA ISH is no more difficult to perform in the IHC lab and is easier to interpret than p16 IHC. HR HPV mRNA ISH is a useful alternative to p16 in cell block specimens.

Identifiants

pubmed: 33092993
pii: S2213-2945(20)30310-0
doi: 10.1016/j.jasc.2020.09.007
pii:
doi:

Substances chimiques

Cyclin-Dependent Kinase Inhibitor p16 0
RNA, Messenger 0
RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

225-230

Informations de copyright

Copyright © 2021 American Society of Cytopathology. Published by Elsevier Inc. All rights reserved.

Auteurs

Bennett L Wilson (BL)

Department of Pathology, University of Rochester, Rochester, New York.

Anna-Karoline Israel (AK)

Department of Pathology, University of Rochester, Rochester, New York.

Abberly A Lott Limbach (AA)

Department of Pathology, University of Rochester, Rochester, New York; Department of Pathology, Ohio State University Wexner Medical Center, Columbus, Ohio. Electronic address: Abberly.lottlimbach@osumc.edu.

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Classifications MeSH