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dc.contributor.authorCraig, SG
dc.contributor.authorAnderson, LA
dc.contributor.authorSchache, AG
dc.contributor.authorMoran, M
dc.contributor.authorGraham, L
dc.contributor.authorCurrie, K
dc.contributor.authorRooney, K
dc.contributor.authorRobinson, M
dc.contributor.authorUpile, NS
dc.contributor.authorBrooker, R
dc.contributor.authorMesri, M
dc.contributor.authorBingham, V
dc.contributor.authorMcQuaid, S
dc.contributor.authorJones, T
dc.contributor.authorMcCance, DJ
dc.contributor.authorSalto-Tellez, M
dc.contributor.authorMcDade, SS
dc.contributor.authorJames, JA
dc.date.accessioned2020-08-28T09:44:04Z
dc.date.issued2019-04-16
dc.identifier.citationBritish journal of cancer, 2019, 120 (8), pp. 827 - 833
dc.identifier.issn0007-0920
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4052
dc.identifier.eissn1532-1827
dc.identifier.doi10.1038/s41416-019-0414-9
dc.description.abstractBACKGROUND: TNM8 staging for oropharyngeal squamous cell carcinomas (OPSCC) surrogates p16 immunohistochemistry for HPV testing. Patients with p16+ OPSCC may lack HPV aetiology. Here, we evaluate the suitability of TNM8 staging for guiding prognosis in such patients. METHODS: HPV status was ascertained using p16 immunohistochemistry and high-risk HPV RNA and DNA in situ hybridisation. Survival by stage in a cohort of OPSCC patients was evaluated using TNM7/TNM8 staging. Survival of p16+/HPV- patients was compared to p16 status. RESULTS: TNM8 staging was found to improve on TNM7 (log rank p = 0·0190 for TNM8 compared with p = 0·0530 for TNM7) in p16+ patients. Patients who tested p16+ but were HPV- (n = 20) had significantly reduced five-year survival (33%) compared to p16+ patients (77%) but not p16- patients (35%). Cancer stage was reduced in 95% of p16+/HPV- patients despite having a mortality rate twice (HR 2.66 [95% CI: 1.37-5.15]) that of p16+/HPV+ patients under new TNM8 staging criteria. CONCLUSION: Given the significantly poorer survival of p16+/HPV- OPSCCs, these data provide compelling evidence for use of an HPV-specific test for staging classification. This has particular relevance in light of potential treatment de-escalation that could expose these patients to inappropriately reduced treatment intensity as treatment algorithms evolve.
dc.formatPrint-Electronic
dc.format.extent827 - 833
dc.languageeng
dc.language.isoeng
dc.publisherSPRINGERNATURE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectPapillomavirus Infections
dc.subjectOropharyngeal Neoplasms
dc.subjectViral Proteins
dc.subjectNeoplasm Staging
dc.subjectDisease-Free Survival
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectAdolescent
dc.subjectAdult
dc.subjectMiddle Aged
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectInfant
dc.subjectInfant, Newborn
dc.subjectFemale
dc.subjectMale
dc.subjectYoung Adult
dc.titleRecommendations for determining HPV status in patients with oropharyngeal cancers under TNM8 guidelines: a two-tier approach.
dc.typeJournal Article
dcterms.dateAccepted2019-02-06
rioxxterms.versionofrecord10.1038/s41416-019-0414-9
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-04
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBritish journal of cancer
pubs.issue8
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Integrated Pathology
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Integrated Pathology
pubs.publication-statusPublished
pubs.volume120
pubs.embargo.termsNot known
icr.researchteamIntegrated Pathology
dc.contributor.icrauthorSalto-Tellez, Manuel


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