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Long-term risk of recurrent cervical human papillomavirus infection and precancer and cancer following excisional treatment

  • Aimée R. Kreimer
  • , Mark Schiffman
  • , Rolando Herrero
  • , Allan Hildesheim
  • , Paula González
  • , Robert D. Burk
  • , Carolina Porras
  • , Mark E. Sherman
  • , Franklin Demuth
  • , Li Cheung
  • , Concepciõn Bratti
  • , Ana Cecilia Rodríguez

Research output: Contribution to journal › Article › peer-review

Abstract

Risk of recurrent CIN2+ (including cervical intraepithelial neoplasia grade 2 [CIN2], CIN3, carcinoma and in situ, adenocarcinoma in situ or cancer) remains elevated for years following treatment. The role of long-term post-treatment human papillomavirus (HPV) presence on subsequent risk of CIN2+ was evaluated in the 10,049-women Guanacaste cohort. Six hundred eighty-one women were referred to colposcopy because of high-grade cytology, positive cervicography and/or suspicion of cancer based on visual assessment; 486 were judged to require treatment. After excluding women with <12 months of follow-up (N = 88), prior cancer or hysterectomy (N = 37) or other reasons (N = 14), 347 were included in the analysis. Infections were categorized as persistent if present at both pre- and post-treatment visits and new if detected only post-treatment. Median time between the treatment and post-treatment visits was 6.7 years (interquartile range 3.8-7.8). At the post-treatment visit, 8 (2.4%), 2 (0.6%) and 8 (2.4%) of the 347 treated women had persistent HPV16, HPV18 or other carcinogenic HPV, respectively. Two (0.8%), 3 (1.0%) and 13 (4.0%) had new HPV16, HPV18 and other carcinogenic HPV, respectively. Six CIN2+ cases were identified at the post-treatment visit, all with persistent infections (three HPV16, one HPV18 and two other carcinogenic HPV). No recurrent disease was observed among women with new HPV infections during the follow-up period. Thus, persistence of HPV infection a median of six years after treatment was uncommon but, when present, posed a substantial risk of subsequent CIN2+. Serial follow-up data from other studies would further strengthen these conclusions.

Original languageEnglish (US)
Pages (from-to)211-218
Number of pages8
JournalInternational Journal of Cancer
Volume131
Issue number1
DOIs
StatePublished - Jul 1 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • HPV
  • LEEP
  • cervical pre-cancer
  • post-treatment
  • recurrence

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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