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Timing, number, and type of sexual partners associated with risk of oropharyngeal cancer.
Drake, Virginia E; Fakhry, Carole; Windon, Melina J; Stewart, C Matthew; Akst, Lee; Hillel, Alexander; Chien, Wade; Ha, Patrick; Miles, Brett; Gourin, Christine G; Mandal, Rajarsi; Mydlarz, Wojciech K; Rooper, Lisa; Troy, Tanya; Yavvari, Siddhartha; Waterboer, Tim; Brenner, Nicole; Eisele, David W; D'Souza, Gypsyamber.
Afiliação
  • Drake VE; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Fakhry C; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Windon MJ; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Stewart CM; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Akst L; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Hillel A; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Chien W; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Ha P; Department of Otolaryngology-Head and Neck Surgery, University of California, San Francisco, San Francisco, California.
  • Miles B; Department of Otolaryngology-Head and Neck Surgery, Mount Sinai Health System, New York City, New York.
  • Gourin CG; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Mandal R; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Mydlarz WK; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • Rooper L; Department of Pathology, Johns Hopkins University, Baltimore, Maryland.
  • Troy T; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Yavvari S; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Waterboer T; Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Program, German Cancer Research Center, Heidelberg, Germany.
  • Brenner N; Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Program, German Cancer Research Center, Heidelberg, Germany.
  • Eisele DW; Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland.
  • D'Souza G; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Cancer ; 127(7): 1029-1038, 2021 04 01.
Article em En | MEDLINE | ID: mdl-33426652
BACKGROUND: Case-control studies from the early 2000s demonstrated that human papillomavirus-related oropharyngeal cancer (HPV-OPC) is a distinct entity associated with number of oral sex partners. Using contemporary data, we investigated novel risk factors (sexual debut behaviors, exposure intensity, and relationship dynamics) and serological markers on odds of HPV-OPC. METHODS: HPV-OPC patients and frequency-matched controls were enrolled in a multicenter study from 2013 to 2018. Participants completed a behavioral survey. Characteristics were compared using a chi-square test for categorical variables and a t test for continuous variables. Adjusted odds ratios (aOR) were calculated using logistic regression. RESULTS: A total of 163 HPV-OPC patients and 345 controls were included. Lifetime number of oral sex partners was associated with significantly increased odds of HPV-OPC (>10 partners: odds ratio [OR], 4.3 [95% CI, 2.8-6.7]). After adjustment for number of oral sex partners and smoking, younger age at first oral sex (<18 vs >20 years: aOR, 1.8 [95% CI, 1.1-3.2]) and oral sex intensity (>5 sex-years: aOR, 2.8 [95% CI, 1.1-7.5]) remained associated with significantly increased odds of HPV-OPC. Type of sexual partner such as older partners when a case was younger (OR, 1.7 [95% CI, 1.1-2.6]) or having a partner who had extramarital sex (OR, 1.6 [95% CI, 1.1-2.4]) was associated with HPV-OPC. Seropositivity for antibodies to HPV16 E6 (OR, 286 [95% CI, 122-670]) and any HPV16 E protein (E1, E2, E6, E7; OR, 163 [95% CI, 70-378]) was associated with increased odds of HPV-OPC. CONCLUSION: Number of oral sex partners remains a strong risk factor for HPV-OPC; however, timing and intensity of oral sex are novel independent risk factors. These behaviors suggest additional nuances of how and why some individuals develop HPV-OPC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comportamento Sexual / Parceiros Sexuais / Neoplasias Orofaríngeas / Infecções por Papillomavirus Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Cancer Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comportamento Sexual / Parceiros Sexuais / Neoplasias Orofaríngeas / Infecções por Papillomavirus Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Cancer Ano de publicação: 2021 Tipo de documento: Article