<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lorenzatti Hiles G</submitter><funding>Ministry of Science and Technology, Taiwan</funding><funding>National Cancer Institute at the National Institutes of Health</funding><funding>Chang Gung Memorial Hospital</funding><funding>University of Michigan Undergraduate Research Opportunity Program</funding><funding>NCI NIH HHS</funding><funding>University of Michigan-Chang Gung Memorial Hospital Pilot Grant</funding><pagination>e0250530</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8064583</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(4)</volume><pubmed_abstract>&lt;h4>Background and objectives&lt;/h4>Human papillomavirus (HPV)-driven oropharyngeal squamous cell carcinoma (OPSCC) is increasing globally. In Taiwan, HPV-positive OPSCC is obscured by tobacco, alcohol, and betel quid use. We investigated the role of high-risk HPV (hrHPV) in a large retrospective Taiwan OPSCC cohort.&lt;h4>Methods and results&lt;/h4>The cohort of 541 OPSCCs treated at Chang Gung Memorial Hospital from 1998-2016 consisted of 507 men (94%) and 34 women (6%). Most used tobacco (81%), alcohol (51%), and betel quid (65%). Formalin-fixed, paraffin-embedded tissue was used for p16 staining (a surrogate marker for HPV) and testing for HPV DNA presence and type by Multiplex HPV PCR-MassArray. HPV DNA and/or p16 staining (HPV-positive) was found in 28.4% (150/528) tumors. p16 and HPV DNA we</pubmed_abstract><journal>PloS one</journal><pubmed_title>Understanding the impact of high-risk human papillomavirus on oropharyngeal squamous cell carcinomas in Taiwan: A retrospective cohort study.</pubmed_title><pmcid>PMC8064583</pmcid><funding_grant_id>CORPG3G0171</funding_grant_id><funding_grant_id>CMRPG3H0852</funding_grant_id><funding_grant_id>MOST 108-2314-B-182A-108-MY3</funding_grant_id><funding_grant_id>CMRPG3J1251</funding_grant_id><funding_grant_id>R01 CA194536</funding_grant_id><funding_grant_id>CA194536</funding_grant_id><funding_grant_id>CA194536-S1</funding_grant_id><pubmed_authors>Wang CI</pubmed_authors><pubmed_authors>Pinatti LM</pubmed_authors><pubmed_authors>Walline HM</pubmed_authors><pubmed_authors>Thomas TB</pubmed_authors><pubmed_authors>Goudsmit CM</pubmed_authors><pubmed_authors>Chang KP</pubmed_authors><pubmed_authors>Yen WC</pubmed_authors><pubmed_authors>Afsari MA</pubmed_authors><pubmed_authors>Carey TE</pubmed_authors><pubmed_authors>Bellile EL</pubmed_authors><pubmed_authors>Morris AC</pubmed_authors><pubmed_authors>Briggs HL</pubmed_authors><pubmed_authors>Peters L</pubmed_authors><pubmed_authors>Jawad N</pubmed_authors><pubmed_authors>Lorenzatti Hiles G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Understanding the impact of high-risk human papillomavirus on oropharyngeal squamous cell carcinomas in Taiwan: A retrospective cohort study.</name><description>&lt;h4>Background and objectives&lt;/h4>Human papillomavirus (HPV)-driven oropharyngeal squamous cell carcinoma (OPSCC) is increasing globally. In Taiwan, HPV-positive OPSCC is obscured by tobacco, alcohol, and betel quid use. We investigated the role of high-risk HPV (hrHPV) in a large retrospective Taiwan OPSCC cohort.&lt;h4>Methods and results&lt;/h4>The cohort of 541 OPSCCs treated at Chang Gung Memorial Hospital from 1998-2016 consisted of 507 men (94%) and 34 women (6%). Most used tobacco (81%), alcohol (51%), and betel quid (65%). Formalin-fixed, paraffin-embedded tissue was used for p16 staining (a surrogate marker for HPV) and testing for HPV DNA presence and type by Multiplex HPV PCR-MassArray. HPV DNA and/or p16 staining (HPV-positive) was found in 28.4% (150/528) tumors. p16 and HPV DNA we</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-06-03T19:27:08.434Z</modification><creation>2025-02-19T03:49:18.342Z</creation></dates><accession>S-EPMC8064583</accession><cross_references><pubmed>33891627</pubmed><doi>10.1371/journal.pone.0250530</doi></cross_references></HashMap>