Kinetics of the Human Papillomavirus Type 16 E6 Antibody Response Prior to Oropharyngeal Cancer
In a European cohort, it was previously reported that 35% of oropharyngeal cancer (OPC) patients were human papillomavirus type-16 (HPV16) seropositive up to 10 years before diagnosis vs 0.6% of cancer-free controls. Here, we describe the kinetics of HPV16-E6 antibodies prior to OPC diagnosis. We us...
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creator | Kreimer, Aimée R Johansson, Mattias Yanik, Elizabeth L Katki, Hormuzd A Check, David P Lang Kuhs, Krystle A Willhauck-Fleckenstein, Martina Holzinger, Dana Hildesheim, Allan Pfeiffer, Ruth Williams, Craig Freedman, Neal D Huang, Wen-Yi Purdue, Mark P Michel, Angelika Pawlita, Michael Brennan, Paul Waterboer, Tim |
description | In a European cohort, it was previously reported that 35% of oropharyngeal cancer (OPC) patients were human papillomavirus type-16 (HPV16) seropositive up to 10 years before diagnosis vs 0.6% of cancer-free controls. Here, we describe the kinetics of HPV16-E6 antibodies prior to OPC diagnosis.
We used annual serial prediagnostic blood samples from the PLCO Cancer Screening Trial. Antibodies to HPV were initially assessed in prediagnostic blood drawn at study enrollment from 198 incident head and neck cancer patients (median years to cancer diagnosis = 6.6) and 924 matched control subjects using multiplex serology, and subsequently in serial samples (median = 5/individual). Available tumor samples were identified and tested for HPV16 RNA to define HPV-driven OPC.
HPV16-E6 antibodies were present at baseline in 42.3% of 52 OPC patients and 0.5% of 924 control subjects. HPV16-E6 antibody levels were highly elevated and stable across serial blood samples for 21 OPC patients who were seropositive at baseline, as well as for one OPC patient who seroconverted closer to diagnosis. All five subjects with HPV16-driven OPC tumors were HPV16-E6-seropositive, and the four subjects with HPV16-negative OPC tumors were seronegative. The estimated 10-year cumulative risk of OPC was 6.2% (95% confidence interval [CI] = 1.8% to 21.5%) for HPV16-E6-seropositive men, 1.3% (95% CI = 0.1% to 15.3%) for HPV16-E6-seropositive women, and 0.04% (95% CI = 0.03% to 0.06%) among HPV16-E6-seronegative individuals.
Forty-two percent of subjects diagnosed with OPC between 1994 and 2009 in a US cohort were HPV16-E6 seropositive, with stable antibody levels during annual follow-up for up to 13 years prior to diagnosis. Tumor analysis indicated that the sensitivity and specificity of HPV16-E6 antibodies were exceptionally high in predicting HPV-driven OPC. |
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We used annual serial prediagnostic blood samples from the PLCO Cancer Screening Trial. Antibodies to HPV were initially assessed in prediagnostic blood drawn at study enrollment from 198 incident head and neck cancer patients (median years to cancer diagnosis = 6.6) and 924 matched control subjects using multiplex serology, and subsequently in serial samples (median = 5/individual). Available tumor samples were identified and tested for HPV16 RNA to define HPV-driven OPC.
HPV16-E6 antibodies were present at baseline in 42.3% of 52 OPC patients and 0.5% of 924 control subjects. HPV16-E6 antibody levels were highly elevated and stable across serial blood samples for 21 OPC patients who were seropositive at baseline, as well as for one OPC patient who seroconverted closer to diagnosis. All five subjects with HPV16-driven OPC tumors were HPV16-E6-seropositive, and the four subjects with HPV16-negative OPC tumors were seronegative. The estimated 10-year cumulative risk of OPC was 6.2% (95% confidence interval [CI] = 1.8% to 21.5%) for HPV16-E6-seropositive men, 1.3% (95% CI = 0.1% to 15.3%) for HPV16-E6-seropositive women, and 0.04% (95% CI = 0.03% to 0.06%) among HPV16-E6-seronegative individuals.
Forty-two percent of subjects diagnosed with OPC between 1994 and 2009 in a US cohort were HPV16-E6 seropositive, with stable antibody levels during annual follow-up for up to 13 years prior to diagnosis. Tumor analysis indicated that the sensitivity and specificity of HPV16-E6 antibodies were exceptionally high in predicting HPV-driven OPC.</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/djx005</identifier><identifier>PMID: 28376197</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Aged ; Antibodies, Viral - blood ; Carcinoma, Squamous Cell - blood ; Carcinoma, Squamous Cell - epidemiology ; Carcinoma, Squamous Cell - virology ; Case-Control Studies ; Cohort Studies ; Female ; Human papillomavirus 16 - immunology ; Humans ; Incidence ; Kinetics ; Male ; Middle Aged ; Oncogene Proteins, Viral - immunology ; Oropharyngeal Neoplasms - blood ; Oropharyngeal Neoplasms - epidemiology ; Oropharyngeal Neoplasms - virology ; Papillomavirus Infections - blood ; Papillomavirus Infections - complications ; Repressor Proteins - immunology ; Risk Factors ; Sensitivity and Specificity ; United States - epidemiology</subject><ispartof>JNCI : Journal of the National Cancer Institute, 2017-08, Vol.109 (8)</ispartof><rights>Published by Oxford University Press 2017. This work is written by US Government employees and is in the public domain in the US.</rights><rights>Published by Oxford University Press 2017. This work is written by US Government employees and is in the public domain in the US. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-341c0d04f64b4f204b4c64f4c49010d08704120d7ec29db52cf30a4b2a56d8253</citedby><cites>FETCH-LOGICAL-c381t-341c0d04f64b4f204b4c64f4c49010d08704120d7ec29db52cf30a4b2a56d8253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28376197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kreimer, Aimée R</creatorcontrib><creatorcontrib>Johansson, Mattias</creatorcontrib><creatorcontrib>Yanik, Elizabeth L</creatorcontrib><creatorcontrib>Katki, Hormuzd A</creatorcontrib><creatorcontrib>Check, David P</creatorcontrib><creatorcontrib>Lang Kuhs, Krystle A</creatorcontrib><creatorcontrib>Willhauck-Fleckenstein, Martina</creatorcontrib><creatorcontrib>Holzinger, Dana</creatorcontrib><creatorcontrib>Hildesheim, Allan</creatorcontrib><creatorcontrib>Pfeiffer, Ruth</creatorcontrib><creatorcontrib>Williams, Craig</creatorcontrib><creatorcontrib>Freedman, Neal D</creatorcontrib><creatorcontrib>Huang, Wen-Yi</creatorcontrib><creatorcontrib>Purdue, Mark P</creatorcontrib><creatorcontrib>Michel, Angelika</creatorcontrib><creatorcontrib>Pawlita, Michael</creatorcontrib><creatorcontrib>Brennan, Paul</creatorcontrib><creatorcontrib>Waterboer, Tim</creatorcontrib><title>Kinetics of the Human Papillomavirus Type 16 E6 Antibody Response Prior to Oropharyngeal Cancer</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>J Natl Cancer Inst</addtitle><description>In a European cohort, it was previously reported that 35% of oropharyngeal cancer (OPC) patients were human papillomavirus type-16 (HPV16) seropositive up to 10 years before diagnosis vs 0.6% of cancer-free controls. Here, we describe the kinetics of HPV16-E6 antibodies prior to OPC diagnosis.
We used annual serial prediagnostic blood samples from the PLCO Cancer Screening Trial. Antibodies to HPV were initially assessed in prediagnostic blood drawn at study enrollment from 198 incident head and neck cancer patients (median years to cancer diagnosis = 6.6) and 924 matched control subjects using multiplex serology, and subsequently in serial samples (median = 5/individual). Available tumor samples were identified and tested for HPV16 RNA to define HPV-driven OPC.
HPV16-E6 antibodies were present at baseline in 42.3% of 52 OPC patients and 0.5% of 924 control subjects. HPV16-E6 antibody levels were highly elevated and stable across serial blood samples for 21 OPC patients who were seropositive at baseline, as well as for one OPC patient who seroconverted closer to diagnosis. All five subjects with HPV16-driven OPC tumors were HPV16-E6-seropositive, and the four subjects with HPV16-negative OPC tumors were seronegative. The estimated 10-year cumulative risk of OPC was 6.2% (95% confidence interval [CI] = 1.8% to 21.5%) for HPV16-E6-seropositive men, 1.3% (95% CI = 0.1% to 15.3%) for HPV16-E6-seropositive women, and 0.04% (95% CI = 0.03% to 0.06%) among HPV16-E6-seronegative individuals.
Forty-two percent of subjects diagnosed with OPC between 1994 and 2009 in a US cohort were HPV16-E6 seropositive, with stable antibody levels during annual follow-up for up to 13 years prior to diagnosis. Tumor analysis indicated that the sensitivity and specificity of HPV16-E6 antibodies were exceptionally high in predicting HPV-driven OPC.</description><subject>Aged</subject><subject>Antibodies, Viral - blood</subject><subject>Carcinoma, Squamous Cell - blood</subject><subject>Carcinoma, Squamous Cell - epidemiology</subject><subject>Carcinoma, Squamous Cell - virology</subject><subject>Case-Control Studies</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Human papillomavirus 16 - immunology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Kinetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oncogene Proteins, Viral - immunology</subject><subject>Oropharyngeal Neoplasms - blood</subject><subject>Oropharyngeal Neoplasms - epidemiology</subject><subject>Oropharyngeal Neoplasms - virology</subject><subject>Papillomavirus Infections - blood</subject><subject>Papillomavirus Infections - complications</subject><subject>Repressor Proteins - immunology</subject><subject>Risk Factors</subject><subject>Sensitivity and Specificity</subject><subject>United States - epidemiology</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUtLxDAUhYMoOj5W7iVLQercPJq2G2EYxgcKiug6pGnqZGiTmrSD8--tjIrexb2Lczj3wIfQKYFLAgWbrpy202r1AZDuoAnhAhJKIN1FEwCaJXme8QN0GOMKxiko30cHNGeZIEU2QfLeOtNbHbGvcb80-HZolcNPqrNN41u1tmGI-GXTGUwEXgg8c70tfbXBzyZ23kWDn4L1AfcePwbfLVXYuDejGjxXTptwjPZq1URz8n2P0Ov14mV-mzw83tzNZw-JZjnpE8aJhgp4LXjJawrj1oLXXPMCyCjkGXBCocqMpkVVplTXDBQvqUpFldOUHaGrbW43lK2ptHF9UI3sgm3HRtIrK_8rzi7lm1_LtBAZS-kYcP4dEPz7YGIvWxu1aRrljB-iJHnOuSAZg9F6sbXq4GMMpv59Q0B-IZFfSOQWyeg--9vs1_vDgH0CEz2JFg</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Kreimer, Aimée R</creator><creator>Johansson, Mattias</creator><creator>Yanik, Elizabeth L</creator><creator>Katki, Hormuzd A</creator><creator>Check, David P</creator><creator>Lang Kuhs, Krystle A</creator><creator>Willhauck-Fleckenstein, Martina</creator><creator>Holzinger, Dana</creator><creator>Hildesheim, Allan</creator><creator>Pfeiffer, Ruth</creator><creator>Williams, Craig</creator><creator>Freedman, Neal D</creator><creator>Huang, Wen-Yi</creator><creator>Purdue, Mark P</creator><creator>Michel, Angelika</creator><creator>Pawlita, Michael</creator><creator>Brennan, Paul</creator><creator>Waterboer, Tim</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170801</creationdate><title>Kinetics of the Human Papillomavirus Type 16 E6 Antibody Response Prior to Oropharyngeal Cancer</title><author>Kreimer, Aimée R ; Johansson, Mattias ; Yanik, Elizabeth L ; Katki, Hormuzd A ; Check, David P ; Lang Kuhs, Krystle A ; Willhauck-Fleckenstein, Martina ; Holzinger, Dana ; Hildesheim, Allan ; Pfeiffer, Ruth ; Williams, Craig ; Freedman, Neal D ; Huang, Wen-Yi ; Purdue, Mark P ; Michel, Angelika ; Pawlita, Michael ; Brennan, Paul ; Waterboer, Tim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-341c0d04f64b4f204b4c64f4c49010d08704120d7ec29db52cf30a4b2a56d8253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Antibodies, Viral - blood</topic><topic>Carcinoma, Squamous Cell - blood</topic><topic>Carcinoma, Squamous Cell - epidemiology</topic><topic>Carcinoma, Squamous Cell - virology</topic><topic>Case-Control Studies</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Human papillomavirus 16 - immunology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Kinetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oncogene Proteins, Viral - immunology</topic><topic>Oropharyngeal Neoplasms - blood</topic><topic>Oropharyngeal Neoplasms - epidemiology</topic><topic>Oropharyngeal Neoplasms - virology</topic><topic>Papillomavirus Infections - blood</topic><topic>Papillomavirus Infections - complications</topic><topic>Repressor Proteins - immunology</topic><topic>Risk Factors</topic><topic>Sensitivity and Specificity</topic><topic>United States - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kreimer, Aimée R</creatorcontrib><creatorcontrib>Johansson, Mattias</creatorcontrib><creatorcontrib>Yanik, Elizabeth L</creatorcontrib><creatorcontrib>Katki, Hormuzd A</creatorcontrib><creatorcontrib>Check, David P</creatorcontrib><creatorcontrib>Lang Kuhs, Krystle A</creatorcontrib><creatorcontrib>Willhauck-Fleckenstein, Martina</creatorcontrib><creatorcontrib>Holzinger, Dana</creatorcontrib><creatorcontrib>Hildesheim, Allan</creatorcontrib><creatorcontrib>Pfeiffer, Ruth</creatorcontrib><creatorcontrib>Williams, Craig</creatorcontrib><creatorcontrib>Freedman, Neal D</creatorcontrib><creatorcontrib>Huang, Wen-Yi</creatorcontrib><creatorcontrib>Purdue, Mark P</creatorcontrib><creatorcontrib>Michel, Angelika</creatorcontrib><creatorcontrib>Pawlita, Michael</creatorcontrib><creatorcontrib>Brennan, Paul</creatorcontrib><creatorcontrib>Waterboer, Tim</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kreimer, Aimée R</au><au>Johansson, Mattias</au><au>Yanik, Elizabeth L</au><au>Katki, Hormuzd A</au><au>Check, David P</au><au>Lang Kuhs, Krystle A</au><au>Willhauck-Fleckenstein, Martina</au><au>Holzinger, Dana</au><au>Hildesheim, Allan</au><au>Pfeiffer, Ruth</au><au>Williams, Craig</au><au>Freedman, Neal D</au><au>Huang, Wen-Yi</au><au>Purdue, Mark P</au><au>Michel, Angelika</au><au>Pawlita, Michael</au><au>Brennan, Paul</au><au>Waterboer, Tim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of the Human Papillomavirus Type 16 E6 Antibody Response Prior to Oropharyngeal Cancer</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>J Natl Cancer Inst</addtitle><date>2017-08-01</date><risdate>2017</risdate><volume>109</volume><issue>8</issue><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>In a European cohort, it was previously reported that 35% of oropharyngeal cancer (OPC) patients were human papillomavirus type-16 (HPV16) seropositive up to 10 years before diagnosis vs 0.6% of cancer-free controls. Here, we describe the kinetics of HPV16-E6 antibodies prior to OPC diagnosis.
We used annual serial prediagnostic blood samples from the PLCO Cancer Screening Trial. Antibodies to HPV were initially assessed in prediagnostic blood drawn at study enrollment from 198 incident head and neck cancer patients (median years to cancer diagnosis = 6.6) and 924 matched control subjects using multiplex serology, and subsequently in serial samples (median = 5/individual). Available tumor samples were identified and tested for HPV16 RNA to define HPV-driven OPC.
HPV16-E6 antibodies were present at baseline in 42.3% of 52 OPC patients and 0.5% of 924 control subjects. HPV16-E6 antibody levels were highly elevated and stable across serial blood samples for 21 OPC patients who were seropositive at baseline, as well as for one OPC patient who seroconverted closer to diagnosis. All five subjects with HPV16-driven OPC tumors were HPV16-E6-seropositive, and the four subjects with HPV16-negative OPC tumors were seronegative. The estimated 10-year cumulative risk of OPC was 6.2% (95% confidence interval [CI] = 1.8% to 21.5%) for HPV16-E6-seropositive men, 1.3% (95% CI = 0.1% to 15.3%) for HPV16-E6-seropositive women, and 0.04% (95% CI = 0.03% to 0.06%) among HPV16-E6-seronegative individuals.
Forty-two percent of subjects diagnosed with OPC between 1994 and 2009 in a US cohort were HPV16-E6 seropositive, with stable antibody levels during annual follow-up for up to 13 years prior to diagnosis. Tumor analysis indicated that the sensitivity and specificity of HPV16-E6 antibodies were exceptionally high in predicting HPV-driven OPC.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>28376197</pmid><doi>10.1093/jnci/djx005</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antibodies, Viral - blood Carcinoma, Squamous Cell - blood Carcinoma, Squamous Cell - epidemiology Carcinoma, Squamous Cell - virology Case-Control Studies Cohort Studies Female Human papillomavirus 16 - immunology Humans Incidence Kinetics Male Middle Aged Oncogene Proteins, Viral - immunology Oropharyngeal Neoplasms - blood Oropharyngeal Neoplasms - epidemiology Oropharyngeal Neoplasms - virology Papillomavirus Infections - blood Papillomavirus Infections - complications Repressor Proteins - immunology Risk Factors Sensitivity and Specificity United States - epidemiology |
title | Kinetics of the Human Papillomavirus Type 16 E6 Antibody Response Prior to Oropharyngeal Cancer |
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