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A prospective cohort study comparing efficacy of 1 dose of quadrivalent human papillomavirus vaccine to 2 and 3 doses at an average follow up of 12 years postvaccination

Journal of the National Cancer Institute - Monographs, ISSN: 1745-6614, Vol: 2024, Issue: 67, Page: 317-328
2024
  • 1
    Citations
  • 0
    Usage
  • 28
    Captures
  • 2
    Mentions
  • 3
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    1
  • Captures
    28
  • Mentions
    2
    • News Mentions
      2
      • News
        2
  • Social Media
    3
    • Shares, Likes & Comments
      3
      • Facebook
        3

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Article Description

Background: While recommending a human papillomavirus (HPV) single-dose vaccination schedule in 2022, the World Health Organization highlighted the need for long-term follow-up studies to monitor waning of protection. We report on vaccine efficacy against HPV infections in 1-, 2-, and 3-dose schedules and protection against cervical precancers at a median follow-up of 12 years postvaccination. Methods: This randomized multicenter study in India was originally designed to vaccinate unmarried girls aged 10-18 years with either 2 or 3 doses of quadrivalent HPV vaccine. A ministerial decree to halt vaccination in trials resulted in the creation of cohorts receiving different doses, including just a single dose. Cohorts were assessed for incident and persistent infections by genotyping cervical samples collected yearly for 4 consecutive years after participants were married. Cervical screening with an HPV test was initiated at age 25 years for married participants. Age- and site-matched unvaccinated married women were recruited to be compared with vaccinated cohorts. Vaccine efficacy was assessed using proportional incidence ratios. Results: The number of participants in the 1-, 2- (at 0 and 6 months), and 3-dose cohorts was 4949, 4980, and 4348, respectively. Of the recipients, 71%-82% in the different cohorts were eligible to provide samples for genotyping. Vaccine efficacy against persistent HPV 16 and 18 infection was 92.0% (95% confidence interval [CI] ¼ 87.0% to 95.0%) in 3022 recipients of the single dose; and comparable with that observed in the 2-dose arm (94.8%, 95% CI ¼ 90.0% to 97.3%) and the 3-dose arm (95.3%, 95% CI ¼ 90.9% to 97.5%). No high-grade precancer associated with HPV 16 and 18 was detected among vaccinated participants compared with 8 precancers detected among the unvaccinated women. Conclusion: This observational cohort study has established that a single dose of HPV vaccine provides high protective efficacy against persistent HPV 16 and 18 infections and associated neoplasia 15 years postvaccination.

Bibliographic Details

Malvi, Sylla G; Esmy, Pulikkottil O; Muwonge, Richard; Joshi, Smita; Poli, Usha Rani Reddy; Lucas, Eric; Verma, Yogesh; Lucksom, Pesona Grace; Shah, Anand; Patel, Bijal; Zomawia, Eric; Pimple, Sharmila; Jayant, Kasturi; Hingmire, Sanjay; Chiwate, Aruna; Divate, Uma; Vashist, Shachi; Mishra, Gauravi; Jadhav, Radhika; Siddiqi, Maqsood; Sauvaget, Catherine; Sankaran, Subha; Kannan, Thiraviam Pillai Rameshwari Ammal; Shastri, Surendra S; Pillai, M Radhakrishna; Anantharaman, Devasena; Bhatla, Neerja; Sankaranarayanan, Rengaswamy; Basu, Partha

Oxford University Press (OUP)

Medicine; Biochemistry, Genetics and Molecular Biology

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