4.5 Article

Investigating a cluster of vulvar cancer in young women: a cross-sectional study of genital human papillomavirus prevalence

期刊

BMC INFECTIOUS DISEASES
卷 12, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1471-2334-12-243

关键词

Human papillomavirus; Population prevalence; Vulvar neoplasms; Young women; Indigenous women

资金

  1. CSL
  2. GSK
  3. Merck
  4. Sanofi Pasteur
  5. MSD
  6. GlaxoSmithKline Australian Postgraduate Support Grant
  7. CSL Biotherapies
  8. National Health and Medical Research Council (NHMRC) in Australia [436013]
  9. Jean B Reid Fellowship from the University of Adelaide Medical Endowment Funds
  10. Royal Women's Hospital Post Graduate Degree Scholarship from the Royal Women's Hospital, Melbourne Australia

向作者/读者索取更多资源

Background: Vulvar cancer is a relatively rare malignancy, which occurs most often in postmenopausal women. We have previously identified a geographic cluster of vulvar cancer in young Indigenous women living in remote communities in the Arnhem Land region of Australia. In this population, we investigated the prevalence of oncogenic human papillomavirus (HPV) infection in anogenital samples (vulvar/vaginal/perianal area and cervix) and compared the overall, type-specific and multiple infection prevalence between sites. Methods: A cross-sectional survey of 551 Indigenous women aged 18-60 years was undertaken in 9 Arnhem Land communities. Women were consented for HPV detection and genotyping collected by a combined vulvar/vaginal/perianal (VVP) sweep swab and a separate PreservCyt endocervical sample collected during Pap cytology screening. HPV DNA testing was undertaken using PCR with broad spectrum L1 consensus PGMY09/11 primers with genotyping of positive samples by Roche Linear Array. The primary outcomes were the prevalence of cervical and VVP high-risk (HR) HPV. Results: The prevalence of VVP HR-HPV was 39%, which was significantly higher than the cervical HR-HPV prevalence (26%, p<0.0001). HPV-16 was the most common genotype detected in both sites (VVP 11%, cervical 6%). HPV-16 infection peaked in women aged <20 years; however, there was a marked decline in cervical HPV-16 prevalence with age (p=0.007), whereas following an initial decline, the prevalence of VVP HPV-16 remained constant in subsequent age-groups (p=0.835). Conclusions: In this population experiencing a cluster of vulvar cancer, the prevalence of cervical oncogenic HPV infection was similar to that reported by studies of other Australian women; however there was a significantly higher prevalence of vulvar/vaginal/perianal infection to cervical. The large discrepancy in HPV prevalence between anogenital sites in this population may represent more persistent infection at the vulva. This needs further investigation, including the presence of possible environmental and/or genetic factors that may impair host immunity.

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