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EP348/#107 Role of HPV in prediction of recurrence/persistence after treatment for cervical precancer
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  1. Anjali Kulkarni1,
  2. Allan Covens2,
  3. Lilian Gien3,
  4. Danielle Vicus2,
  5. Ray Osborne2,
  6. Nancy Durand4,
  7. Zeina Ghorab5 and
  8. Rachel Kupets6
  1. 1University of Ottawa, Gynecologic Oncology, Ottawa, Canada
  2. 2Sunnybrook Odette Cancer Center, Division of Gynecologic Oncology, Toronto, Canada
  3. 3Sunnybrook Odette Cancer Centre, Division of Gynecologic Oncology, Toronto, Canada
  4. 4Sunnybrook Health Sciences Center, Obstetrics and Gynecology, Toronto, Canada
  5. 5Sunnybrook Health Sciences Center, Gynecologic Pathology, Toronto, Canada
  6. 6Sunnybrook Health Sciences Center, Gynecologic Oncology, Toronto, Canada

Abstract

Objectives 1. To determine the role of HPV testing after excisional treatment of cervical precancer. 2. To determine clinical factors associated with persistence of cervical precancer post-treatment.

Methods A retrospective chart review was conducted on patients who had a LEEP for cervical precancer (CIN3/AIS/HSIL) between 2016–2018 at a colposcopy unit in a university-affiliated centre in Toronto. Persistence/recurrence of disease was defined as a finding of high-grade cytology or pathology results during the time of follow-up. Univariate and multivariate regression models were run with persistence/recurrence and HPV positivity at exit testing as an outcome.

Results A total of 284 patients were included. The median follow-up time was 19 months. Of the LEEP specimens, 90.8% (n=258) demonstrated HSIL and 3.9% (n=11) had AIS. 28.5% (n=81) of the LEEP specimens had positive margins. In follow-up, 72.9% had negative cytology, 17.6% had ASCUS/LSIL, 1.8% had ASC-H/LSIL-H and 6.7% had HSIL. At the final follow-up, 27.8% (n=79) were HPV+. Overall rate of persistence/recurrence was 11.3% (n=32); median time to persistence/recurrence was 6.5 months. Multivariate regression models demonstrated that follow-up HPV positivity (OR=22.0) and positive margins (OR=3.7) were significant for predicting persistence/recurrence. Similarly, in univariate regression models, positive margins were significant (OR=2.2) for predicting HPV positivity in exit testing.

Conclusions Persistence/recurrence of precancer can occur due to incomplete treatment of lesions by local excision and by persistence of HPV infection. Surveillance strategies for women treated for cervical precancer require a risk-based approach such as that suggested in the ASCCP guidelines.

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