Journal of Clinical Medicine (Sep 2021)

Intra-Anal Imiquimod Cream against Human Papillomavirus Infection in Men Who Have Sex with Men Living with HIV: A Single-Arm, Open-Label Pilot Study

  • Duygu Durukan,
  • Tiffany R. Phillips,
  • Gerald L. Murray,
  • Jason J. Ong,
  • Andrew E. Grulich,
  • I. Mary Poynten,
  • Fengyi Jin,
  • Catriona S. Bradshaw,
  • Ivette Aguirre,
  • Julie Silvers,
  • Helen Kent,
  • Steph Atchison,
  • Prisha Balgovind,
  • Alyssa Cornall,
  • Marcus Y. Chen,
  • Christopher K. Fairley,
  • Eric P. F. Chow

DOI
https://doi.org/10.3390/jcm10194477
Journal volume & issue
Vol. 10, no. 19
p. 4477

Abstract

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Men who have sex with men (MSM) living with HIV have a high prevalence and incidence of anal high-risk human papillomavirus (hrHPV) and anal cancer. We conducted an open-label, single-arm pilot study to examine the tolerability of imiquimod cream among MSM aged ≥18 years, living with HIV, who tested positive for anal hrHPV at Melbourne Sexual Health Centre between April 2018 and June 2020. We instructed men to apply 6.25 mg imiquimod intra-anally and peri-anally 3 doses per week for 16 weeks (period 1) and then one dose per week for a further 48 weeks (period 2). Twenty-seven MSM enrolled in period 1 and 24 (86%) applied at least 50% of doses. All men reported adverse events (AEs), including 39.5% grade 1, 39.5% grade 2, and 21% grade 3 AEs on at least one occasion. Eighteen MSM (67%) temporarily stopped using imiquimod during period 1, most commonly due to local AEs (n = 11) such as irritation and itching. Eighteen MSM continued in period 2 and all applied at least 50% of doses with no treatment-limiting AEs reported. Imiquimod 3 doses per week caused local AEs in most men and was not well tolerated. In contrast, once-a-week application was well tolerated over 48-weeks with no treatment-limiting AEs.

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