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Human papillomavirus detection in cervical neoplasia attributed to 12 high-risk human papillomavirus genotypes by region

  • Xavier Castellsagué(corresponding author)
    ,
  • Kevin A. Ault
    ,
  • F. Xavier Bosch
    ,
  • Darron Brown
    ,
  • Jack Cuzick
    ,
  • Daron G. Ferris
*Corresponding author for this work
  • Bellvitge Biomedical Research Institute
    ,
  • University of Kansas
    ,
  • Indiana University-Purdue University Indianapolis
    ,
  • Queen Mary University of London
    ,
  • ,
  • Medical University of Vienna
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Background: We estimated the proportion of cervical intraepithelial neoplasia (CIN) cases attributed to 14 HPV types, including quadrivalent (qHPV) (6/11/16/18) and 9-valent (9vHPV) (6/11/16/18/31/33/45/52/58) vaccine types, by region. Methods: Women ages 15-26 and 24-45 years from 5 regions were enrolled in qHPV vaccine clinical trials. Among 10,706 women (placebo arms), 1539 CIN1, 945 CIN2/3, and 24 adenocarcinoma in situ (AIS) cases were diagnosed by pathology panel consensus. Results: Predominant HPV types were 16/51/52/56 (anogenital infection), 16/39/51/52/56 (CIN1), and 16/31/52/58 (CIN2/3). In regions with largest sample sizes, minimal regional variation was observed in 9vHPV type prevalence in CIN1 (~50%) and CIN2/3 (81-85%). Types 31/33/45/52/58 accounted for 25-30% of CIN1 in Latin America and Europe, but 14-18% in North America and Asia. Types 31/33/45/52/58 accounted for 33-38% of CIN2/3 in Latin America (younger women), Europe, and Asia, but 17-18% of CIN2/3 in Latin America (older women) and North America. Non-vaccine HPV types 35/39/51/56/59 had similar or higher prevalence than qHPV types in CIN1 and were attributed to 2-11% of CIN2/3. Conclusions: The 9vHPV vaccine could potentially prevent the majority of CIN1-3, irrespective of geographic region. Notwithstanding, non-vaccine types 35/39/51/56/59 may still be responsible for some CIN1, and to a lesser extent CIN2/3.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 61-69 (9 pages)

Journal (Volume, Issue Number)

Papillomavirus Research (Volume 2)

Publication milestones

  • Published - 12/01/2016

Publication status

Published - 12/01/2016

Publication IDs

  • Scopus: 84961675401
  • PubMed: 29074187

Publication metrics

Metrics

SciVal
FWCI
1.43
SciVal
Author count
26
SciVal
citations
20
SciVal
Paper percentile
85
Scopus
citations
Fractional count
1
Fractional count
0.04
Fractional count
25
Fractional count
0.96
Fractional count
1
Fractional count
1

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Citation count
33
Mentions
1
Captures
100

Funding Details

Xavier Castellsagué reports having received institutional research grants from Merck and Co., Inc., Sanofi Pasteur MSD, GlaxoSmithKline, and Genticel, and occasional personal travel grant and speakers honorarium from Sanofi Pasteur MSD and Vianex Kevin A. Ault reports having received grants to his institution from Merck and the National Institutes of Health and advisory committee fees from the American College of Obstetricians and Gynecologists. He also serves on the editorial board for the National Cancer Institute (USA). This study was funded by Merck and Co., Inc. , Kenilworth, NJ (ClinicalTrials.gov: NCT00092521 , NCT00092534 , and NCT00090220 ). This systematic review was designed, managed, and analyzed jointly by authors employed by Merck & Co. and external authors who were not paid for their work. Susanne K. Kjaer reports having received scientific advisory board and speaker׳s fees and unrestricted research grants through her institution from Sanofi Pasteur MSD and Merck, and scientific advisory board fee from Roche.