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Pre-diagnostic dynamic HPV16 IgG seropositivity and risk of oropharyngeal cancer.
Anderson, Karen S; Wallstrom, Garrick; Langseth, Hilde; Posner, Marshall; Cheng, Julia N; Alam, Rizwan; Chowell, Diego; Furre, Ingegerd E; Mork, Jon.
Affiliation
  • Anderson KS; Center for Personalized Diagnostics, The Biodesign Institute, Arizona State University, Tempe, AZ, United States. Electronic address: Karen.Anderson.1@asu.edu.
  • Wallstrom G; Center for Personalized Diagnostics, The Biodesign Institute, Arizona State University, Tempe, AZ, United States.
  • Langseth H; Cancer Registry of Norway, Institute of Population-based Cancer Research,; Department of Research, Oslo, Norway.
  • Posner M; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York City, NY, United States.
  • Cheng JN; Center for Personalized Diagnostics, The Biodesign Institute, Arizona State University, Tempe, AZ, United States.
  • Alam R; Center for Personalized Diagnostics, The Biodesign Institute, Arizona State University, Tempe, AZ, United States.
  • Chowell D; Center for Personalized Diagnostics, The Biodesign Institute, Arizona State University, Tempe, AZ, United States; Simon A. Levin Mathematical, Computational, and Modeling Sciences Center, Arizona State University, Tempe, AZ, United States.
  • Furre IE; Department of Pathology, Oslo University Hospital, Oslo, Norway.
  • Mork J; Department of Otolaryngology, Oslo University Hospital, Oslo, Norway.
Oral Oncol ; 73: 132-137, 2017 10.
Article in En | MEDLINE | ID: mdl-28939065
ABSTRACT

OBJECTIVE:

The aim of this study was to determine the association of HPV16 antibodies (Abs) and oropharyngeal cancer (OPC) risk in sera obtained prior to clinical diagnosis.

METHODS:

We identified 92 participants with incident OPC and 460 matched controls from the Janus Serum Bank Cohort in Norway. Archived tumor specimens were requested for a subset of the cases. Serum samples were collected from cases, on average, 9.3years before diagnosis (range, 0.1-14.9years). Ten cases had serum samples from multiple time points. IgG seropositivity to 8 HPV16 antigens was determined, and a logistic regression classifier of a panel of all early-antigen (EA) Abs for the predictive diagnosis of OPC was applied.

RESULTS:

HPV16 EA seropositivity was present in 25.0% of patients with OPC and 7.6% of controls (odds ratio (OR), 4.1; 95% CI, 2.3-7.2, p<0.0001). Abs to E2 were strongly associated with cases 0-2years pre- diagnosis (OR, 150.1; 95% CI, 27.4-1040.0, p<0.0001), and the probability of seropositivity was inversely associated with time to diagnosis (OR, 0.7 per additional year; 95% CI, 0.6-0.9, p=0.0002). Abs to E2 were also strongly associated with tumor HPV status (OR, 35.6; 95% CI, 8.7-200.0, p<0.0001). A positive score on the binary classifier was associated with an overall OR of 15.8 (95% CI, 5.6-53.4) compared with controls (p<0.05), and was strongly associated with tumor HPV status (OR, 27.4; 95% CI, 8.6-99.6, p<0.001).

CONCLUSIONS:

HPV16 Abs are detectable years prior to diagnosis of OPC, and the probability of seropositivity increases closer to diagnosis.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunoglobulin G / Oropharyngeal Neoplasms / Human papillomavirus 16 Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Oral Oncol Journal subject: NEOPLASIAS Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunoglobulin G / Oropharyngeal Neoplasms / Human papillomavirus 16 Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Oral Oncol Journal subject: NEOPLASIAS Year: 2017 Document type: Article