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2022-RA-1032-ESGO Evaluation of intraoperative HPV test as an early marker of residual disease after HSIL surgical treatment. a prospective multicenter study. Preliminary results
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  1. Melissa Bradbury1,
  2. Ursula Acosta1,
  3. Alfonso Quesada2,
  4. Jose A Lopez-Fernandez3,
  5. Jose Quilez4,
  6. Cristina Centeno1,
  7. Antonio Gil1,
  8. Multicenter VPH IOP Team
  1. 1Gynecology, Hospital Vall d’Hebron. Barcelona SPAIN, Barcelona, Spain
  2. 2Gynecology, Hospital Nuestra Señora de la Candelaria, Tenerife, Spain
  3. 3Gynecology, Hospital General Alicante, Alicante, Spain
  4. 4Gynecolgy, Hospital de Basurto, Bilbao, Spain

Abstract

Objective To evaluate if the intraoperative human papillomavirus (IOP-HPV) test has the same prognostic value as the HPV test performed 6 months after treatment of high-grade squamous intraepithelial Lesion (HSIL) to predict treatment failure.

Design Prospective multicenter cohort studySetting: 22 Referral Hospitals in Spain.Population: 1824 women treated for cervical HSIL by Loop Electrosurgical Excision between May 2020 and December 2021

After LEEP an HPV test was performed immediately after excision using a Cobas (83%) or other genotyping test.

Subsequently, pacients were followed with citology and HPV test, 6, 12 and 24 months after treatment.

The IOP-HPV test was compared with HPV test 6 months after procedure and with surgical margins in order to detect residual disease.

Results We described results of the first 992 cases with the 6 month co-test performed. IOP HPV test was feasible (valid result 98,5%). IOP-HPV was positive in 40%, while only 25% at 6 month test. We observed association between the IOP and 6 month HPV test (ChiSquare p= 0.0001), IOP HPV positivity and abnormal citology at 6 months (p=0.063), and positive IOP HPV test and positive surgical margins.(p=0.0001)

Conclusion Preliminary results show that IOP HPV test could be a satisfactory prognostic factor of cervical HSIL treatment result.

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