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P501 Low prevalence of high-risk anal HPV in young gay and bisexual males after the universal HPV vaccination program in australia
  1. Eric Chow1,
  2. Sepehr Tabrizi2,
  3. Christopher Fairley1,
  4. Rebecca Wigan1,
  5. Alyssa Cornall2,
  6. Steph Atchison2,
  7. Dorothy Machalek2,
  8. Jane Hocking3,
  9. Catriona Bradshaw1,
  10. Suzanne Garland2,
  11. Marcus Chen1
  1. 1Alfred Health, Melbourne Sexual Health Centre, Carlton, Australia
  2. 2The Royal Women’s Hospital, Centre for Women’s Infectious Disease Research, Parkville, Australia
  3. 3University of Melbourne, Melbourne School of Population and Global Health, Parkville, Australia

Abstract

Background Australia introduced a school-based quadrivalent human papillomavirus (HPV) vaccination program for females in 2007. This was extended to include boys aged 12–13 from 2013, with a two-year catch-up for boys aged ≤15. This study examined HPV prevalence among young gay and bisexual males (GBM) who were age-eligible for vaccination in the school-based program.

Methods Males aged 16–20 years were recruited from sexual health clinics and the community in Melbourne in 2017–2018, if they reported any form of male sexual contact, and were residents of Australia from 2013. A clinician-collected anal swab, self-collected penile swab and oral rinse were collected and analysed for detection and 37 HPV genotypes (Roche Linear Array). Preliminary results from 114 GBM were analysed and full results will be available for presentation.

Results The mean age of GBM was 18.6 years (SD 1.0). The majority (80%) were recruited from clinics and 20% from the community. The median number of lifetime male partners was 10 [IQR 5–25] for receptive oral sex, four [IQR 1–11] for receptive anal sex and one for insertive anal sex [IQR 0–6]. Overall, 64% received at least one dose of vaccine documented via the National HPV Vaccination Program Register. Prevalence of quadrivalent vaccine-preventable HPV genotypes was 4.9% (95% CI: 1.6–11%) for anal, 3.4% (95% CI: 0.7–9.5%) for penile and 0% (95% CI: 0–3.2%) for oral sites. Only two men, both unvaccinated, had high-risk vaccine-preventable HPV genotypes: one with anal HPV16 (1%); the other penile HPV16 (1%).

Conclusion Statistical analysis comparing before and after the male vaccination program will be performed until recruitment is completed. The preliminary analysis shows the prevalence of anal HPV 16/18 among young GBM following the school-based male HPV vaccination was low. The addition of male HPV vaccination to female programs may reduce the incidence of anal cancer among GBM.

Disclosure No significant relationships.

  • HPV
  • prevention
  • intervention and treatment
  • modeling and prevalence
  • gay and bisexual men and other men who have sex with men

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