Evidence map›Paper›PMID 31666283›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2020

Comparison of Molecular Assays for HPV Testing in Oropharyngeal Squamous Cell Carcinomas: A Population-Based Study in Northern Ireland.

Stephanie G Craig, Lesley A Anderson, Michael Moran, Laura Graham, Keith Currie, Keith Rooney, Max Robinson, Victoria Bingham, Kate S Cuschieri, Stephen McQuaid and 6 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 3 syntheses or guidelines pooled it, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 4 countries.

Stephanie G CraigNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Lesley A AndersonNorthern Ireland Cancer Registry, Belfast, Northern Ireland, United Kingdom.
Michael MoranPfizer Pharma GmbH, Berlin, Germany.
Laura GrahamNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Keith CurrieNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Keith RooneyNorthern Ireland Cancer Centre, Belfast, Northern Ireland, United Kingdom.ORCID 0000-0003-0376-1676
Max RobinsonCentre for Oral Health Research, Newcastle University, England, United Kingdom.ORCID 0000-0003-4491-6865
Victoria BinghamNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Kate S CuschieriNational Health Service Lothian, Edinburgh, Scotland, United Kingdom.
Stephen McQuaidNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.ORCID 0000-0003-0794-8569
Andrew G SchacheLiverpool Head and Neck Centre, Institute of Translational Medicine, University of Liverpool, England, United Kingdom.ORCID 0000-0001-9466-6038
Terry M JonesLiverpool Head and Neck Centre, Institute of Translational Medicine, University of Liverpool, England, United Kingdom.ORCID 0000-0002-4058-6013
Dennis McCanceDepartment of Pathology and the University of New Mexico Comprehensive Cancer Centre, University of New Mexico Medical School, Albuquerque, New Mexico.
Manuel Salto-TellezNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.
Simon S McDadeCentre for Cell Research and Cell Biology, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.ORCID 0000-0002-3024-4773
Jacqueline A JamesNorthern Ireland Molecular Pathology Laboratory, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom. j.james@qub.ac.uk.
Queen's University Belfast · GBUniversity of Liverpool · GBNew Mexico Cancer Center · USNHS Lothian · GBPharmaZell (Germany) · DEThe Northern Ireland Cancer Centre · GBUniversity of Newcastle Australia · AU

Funding

Study of genomic instability caused by HPV16 E6 and E7R01DE015935 · NIDCR · UNIVERSITY OF ROCHESTER · PI MCCANCE, DENNIS J. · 2004 to 2008
$1.6M
CO-ACTIVATOR FUNCTION IN ORAL CANCER CELLSR01DE013526 · NIDCR · UNIVERSITY OF ROCHESTER · PI MCCANCE, DENNIS J. · 2000 to 2004
$1.4M
Cancer Research UK 20256Cancer Research UK R2111CNRMedical Research Council G0700754Medical Research Council G1001692Medical Research Council MR/N005872/1Medical Research Council R1310CNRMedical Research Council R4556CNRNIDCR NIH HHS R01 DE013526NIDCR NIH HHS R01 DE015935Wellcome TrustWellcome Trust WT093893MA
6 · The paper itself

Abstract

backgroundDetermination of human papillomavirus (HPV) status has become clinically relevant for patient stratification under UICC TNM8 staging. Within the United Kingdom, a combination of p16 IHC and HPV DNA-ISH is recommended for classifying HPV status. This study will assess a series of clinically applicable second-line molecular tests to run in combination with p16 IHC to optimally determine HPV status.

methodsThe ability of HPV RNA-ISH, HPV DNA-ISH, and HPV DNA-PCR to identify p16-positive/HPV-positive patients was investigated in a population-based oropharyngeal squamous cell carcinoma (OPSCC) cohort of patients diagnosed in Northern Ireland from 2000 to 2011.

resultsOnly 41% of the Northern Irish OPSCC patient population was associated with HPV-driven carcinogenesis. Both ISH assays were more specific than the DNA-PCR assay (100% and 95% vs. 67%) and were less likely to be affected by preanalytic factors such as increasing block age. A pooled HPV genotype probe for RNA-ISH was found to be the most accurate molecular assay assessed (95% accuracy) when compared with p16 positivity.

conclusionsOur study demonstrates the advantage of tissue-based molecular assays when determining HPV status in retrospective samples. Specifically, we demonstrate the enhanced sensitivity and specificity of ISH techniques compared with PCR-based methodology when working with formalin-fixed paraffin-embedded tissue, and found HPV RNA-ISH to be the most effective assay for determining HPV status. IMPACT: As p16 IHC is a relatively inexpensive, accessible, and sensitive test for stratifying patients by HPV status, this study finds that more patients would benefit from first-line p16 IHC followed by specific HPV testing using HPV RNA-ISH to confirm HPV status.

Indexed as

Age FactorsAlphapapillomavirusBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16DNA, ViralFemaleFollow-Up StudiesHuman Papillomavirus DNA TestsHumansImmunohistochemistryIn Situ HybridizationKaplan-Meier EstimateMaleMiddle AgedNeoplasm StagingNorthern IrelandBiomarkers, TumorCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16DNA, ViralRNA, Viral

Identifiers

PMID31666283
PMCPMC9158515
OpenAlexW2982673251

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.