Abstract 211: Association between prior smoking and the time between HPV16-E6 seroconversion and development of oropharyngeal squamous cell carcinoma.

Abstract Background and aims: Human papillomavirus (HPV) type 16 E6 oncoprotein antibodies in peripheral blood are a strong marker of oropharyngeal squamous cell carcinoma (OPSCC). In a previous study, HPV16-E6 seroconversion was observed from 6 to 28 years before cancer diagnosis. In the present study, the serology measurements were complemented with DNA and RNA genotyping of HPV from cancer tissue from the same OPSCC patients. We aimed to refine estimates of timing of and age at HPV16-E6 seroconversion before HPV-driven OPSCC and to investigate their dependence on notable covariates such as tobacco use. Patients and methods: 307 OPSCC cases were identified from the prospective Janus Serum Bank Cohort in Norway enrolled from 1972 to 2004. Pre-diagnostic samples were analyzed for antibodies against proteins of HPV16 and other oncogenic HPV types by multiplex serology. Diagnostic formalin-fixed paraffin-embedded tumor blocks were obtained from different hospitals and HPV DNA and RNA genotyped by Multiplex Papillomavirus Genotyping and HPV type-specific E6*I RNA assays. Cancers positive for DNA and RNA of the same HPV type were regarded as HPV-driven. Information about smoking status was available from questionnaires. For every HPV16-driven cancer, an age and time interval for HPV16-E6 seroconversion was inferred and the Turnbull estimator for interval-censored data was applied. Results: Out of 242 OPSCC cases with a retrieved and successfully sectioned tumor block, 221 (83.7%) had a valid HPV DNA/RNA cancer tissue test. The proportion of OPSCC driven by HPV increased rapidly from 1990 (0%) to 2010 (over 60%). The majority of the HPV-driven OPSCC cases were caused by HPV16 (55.2% of all OPSCC cases), followed by HPV33 (5.4%). All patients developing HPV16-driven cancer within 10 years from blood draw were HPV16-E6 seropositive at blood draw. The estimated median age of HPV16-E6 seroconversion for HPV16 driven cancers was 43 years with an interquartile range (IQR) of 41-46, and the median time from seroconversion to HPV16-driven cancer was 16 years (IQR: 12-22). Current smokers had a much shorter time from seroconversion to cancer than former and never smokers (median of 14 vs 18 and 21 years). Conclusions: The high sensitivity and specificity of HPV16-E6 seropositivity makes it a promising early biomarker for HPV-driven OPSCC. HPV16-E6 seropositive individuals that were smokers at the time of blood draw developed HPV16-driven OPSCC 8 years earlier than seropositive individuals that never smoked, suggesting intensified follow-up of HPV16-E6 seropositive smokers. The age at HPV16-E6 seroconversion indicates that many cancer-causing HPV infections are acquired after mid-20s, with the implication that young adults would benefit from HPV vaccination for prevention against oropharyngeal cancer. Citation Format: Ståle Nygård, Lea Schroeder, Marie Gulla, Aida Ferreiro-Iglesias, Paul Brennan, Hilde Langseth, Giske Ursin, Aimée R. Kreimer, Mattias Johansson, Hilary Robbins, Tim Waterboer, Mari Kiens Nygard. Association between prior smoking and the time between HPV16-E6 seroconversion and development of oropharyngeal squamous cell carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 211.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-211
Primary Topic
Head and Neck Cancer Studies
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article
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article

Abstract 211: Association between prior smoking and the time between HPV16-E6 seroconversion and development of oropharyngeal squamous cell carcinoma.

M. Johansson, Hilary A. Robbins, Aida Ferreiro-Iglesias, Hilde Langseth et al.
Cancer Research
Head and Neck Cancer Studies
article

Abstract 211: Association between prior smoking and the time between HPV16-E6 seroconversion and development of oropharyngeal squamous cell carcinoma.

M. Johansson, Hilary A. Robbins, Aida Ferreiro-Iglesias, Hilde Langseth, Giske Ursin, Paul Brennan, Lea Schroeder, T. Waterboer, Marie Gulla, Mari Kiens Nygard, Aimée R. Kreimer, Ståle Nygård
article en

Abstract

Abstract Background and aims: Human papillomavirus (HPV) type 16 E6 oncoprotein antibodies in peripheral blood are a strong marker of oropharyngeal squamous cell carcinoma (OPSCC). In a previous study, HPV16-E6 seroconversion was observed from 6 to 28 years before cancer diagnosis. In the present study, the serology measurements were complemented with DNA and RNA genotyping of HPV from cancer tissue from the same OPSCC patients. We aimed to refine estimates of timing of and age at HPV16-E6 seroconversion before HPV-driven OPSCC and to investigate their dependence on notable covariates such as tobacco use. Patients and methods: 307 OPSCC cases were identified from the prospective Janus Serum Bank Cohort in Norway enrolled from 1972 to 2004. Pre-diagnostic samples were analyzed for antibodies against proteins of HPV16 and other oncogenic HPV types by multiplex serology. Diagnostic formalin-fixed paraffin-embedded tumor blocks were obtained from different hospitals and HPV DNA and RNA genotyped by Multiplex Papillomavirus Genotyping and HPV type-specific E6*I RNA assays. Cancers positive for DNA and RNA of the same HPV type were regarded as HPV-driven. Information about smoking status was available from questionnaires. For every HPV16-driven cancer, an age and time interval for HPV16-E6 seroconversion was inferred and the Turnbull estimator for interval-censored data was applied. Results: Out of 242 OPSCC cases with a retrieved and successfully sectioned tumor block, 221 (83.7%) had a valid HPV DNA/RNA cancer tissue test. The proportion of OPSCC driven by HPV increased rapidly from 1990 (0%) to 2010 (over 60%). The majority of the HPV-driven OPSCC cases were caused by HPV16 (55.2% of all OPSCC cases), followed by HPV33 (5.4%). All patients developing HPV16-driven cancer within 10 years from blood draw were HPV16-E6 seropositive at blood draw. The estimated median age of HPV16-E6 seroconversion for HPV16 driven cancers was 43 years with an interquartile range (IQR) of 41-46, and the median time from seroconversion to HPV16-driven cancer was 16 years (IQR: 12-22). Current smokers had a much shorter time from seroconversion to cancer than former and never smokers (median of 14 vs 18 and 21 years). Conclusions: The high sensitivity and specificity of HPV16-E6 seropositivity makes it a promising early biomarker for HPV-driven OPSCC. HPV16-E6 seropositive individuals that were smokers at the time of blood draw developed HPV16-driven OPSCC 8 years earlier than seropositive individuals that never smoked, suggesting intensified follow-up of HPV16-E6 seropositive smokers. The age at HPV16-E6 seroconversion indicates that many cancer-causing HPV infections are acquired after mid-20s, with the implication that young adults would benefit from HPV vaccination for prevention against oropharyngeal cancer. Citation Format: Ståle Nygård, Lea Schroeder, Marie Gulla, Aida Ferreiro-Iglesias, Paul Brennan, Hilde Langseth, Giske Ursin, Aimée R. Kreimer, Mattias Johansson, Hilary Robbins, Tim Waterboer, Mari Kiens Nygard. Association between prior smoking and the time between HPV16-E6 seroconversion and development of oropharyngeal squamous cell carcinoma [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 211.

Cancer ResearchVol. 86(7_Supplement)
Norwegian Institute of Public Health (NO), German Cancer Research Center (DE), Heidelberg University (DE), Cancer Genetics (United States) (US), Centre international de recherche sur le cancer (FR)
Good health and well-being
Openalex Percentile: Top 4%
Head and Neck Cancer Studies
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