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Topical imiquimod treatment of residual or recurrent cervical intraepithelial neoplasia lesions (TOPIC-2): A randomised controlled trial.

Authors :
van de Sande AJM
van Baars R
Koeneman MM
Gerestein CG
Kruse AJ
van Esch EMG
de Vos van Steenwijk PJ
Muntinga CLP
Willemsen SP
van Doorn HC
van Kemenade FJ
van Beekhuizen HJ
Source :
BJOG : an international journal of obstetrics and gynaecology [BJOG] 2024 Mar 31. Date of Electronic Publication: 2024 Mar 31.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Objective: To investigate the efficacy of imiquimod in women with residual or recurrent cervical intraepithelial neoplasia (rrCIN), compared with large loop excision of the transformation zone (LLETZ).<br />Design: Randomised controlled non-inferiority trial.<br />Setting: One academic and one regional hospital in the Netherlands.<br />Population: Thirty-five women with rrCIN were included in the study between May 2016 and May 2021.<br />Methods: Women were randomised to receive treatment with 5% imiquimod cream (12.5 mg) intravaginally (three times a week for a duration of 16 weeks) or a LLETZ procedure (standard treatment).<br />Main Outcome Measures: The primary outcome was reduction to normal cytology at 6 months after starting treatment. Secondary outcomes were clearance of high-risk human papilloma virus (hr-HPV) in both groups and reduction to ≤CIN1 in the imiquimod group. Side effects were monitored.<br />Results: Treatment success was 33% (6/18) in the imiquimod group versus 100% (16/16) in the LLETZ group (P < 0.001), whereas HPV clearance was 22% (4/18) in the imiquimod group versus 88% (14/16) in the LLETZ group (P < 0.001). After the randomisation of 35 women, the futility of treatment with imiquimod was proven and the trial was prematurely finished. In the follow-up period, three patients remained without additional treatment, whereas all other patients underwent LLETZ, conisation or hysterectomy. In the LLETZ group none of the patients received additional treatment during 2 years of follow-up.<br />Conclusions: This is the first randomised controlled trial to show that topical imiquimod has a significantly lower success rate in terms of reduction to normal cytology and hr-HPV clearance, compared with LLETZ, in women with rrCIN. Additionally, imiquimod has numerous side effects and after using imiquimod most women with rrCIN still required additional surgical treatment.<br /> (© 2024 The Authors. BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1471-0528
Database :
MEDLINE
Journal :
BJOG : an international journal of obstetrics and gynaecology
Publication Type :
Academic Journal
Accession number :
38556619
Full Text :
https://doi.org/10.1111/1471-0528.17808