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Peer-reviewedCC BYBMC women's health

Long-term follow-up results of topical imiquimod for high-grade cervical intraepithelial neoplasia in young women: an original research.

4 affiliations
  1. 1Department of Obstetrics and Gynecology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Republic of Korea.
  2. 2Department of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.
  3. 3Department of Obstetrics and Gynecology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
  4. 4Department of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea. [email protected].

Abstract

Background

Cervical excisional treatment is associated with adverse obstetric outcomes. Although imiquimod has been explored as a conservative alternative in trials like TOPIC-3, its definitive role remains debated. We aimed to evaluate the long-term efficacy of a clinician-applied imiquimod strategy specifically in women aged under 35 years to verify its potential for fertility preservation.Methods

We conducted a retrospective, single-arm cohort study of nulliparous women aged under 35 years with Cervical Intraepithelial Neoplasia (CIN) 2 or 3 and no prior excisional therapy between October 2021 and March 2024. The primary outcomes were histological regression assessed immediately post-treatment (8 weeks) and during a prolonged follow-up period.Results

A total of 100 patients were included. The immediate regression rate following the 8-week imiquimod course was 96.0%, with an initial high risk Human Papillomavirus (hr-HPV) clearance rate of 57.1%. In the follow-up analysis, the sustained regression rate reached 91.0%, and the cumulative hr-HPV clearance rate rose to 70.5%. Notably, patients with CIN2 without HPV 16/18 achieved the highest regression rate (96.5%), successfully avoided or postponed surgical intervention.Conclusions

The clinician-applied imiquimod strategy offers a robust therapeutic impact, safely postponing surgical intervention for approximately one year in reproductive-aged women with CIN 2/3. This imiquimod strategy serves as an effective bridging therapy that preserves fertility without compromising clinical safety, providing a supportive clinical decision-making model for individualized non-surgical management.

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BibTeX
@article{kim2026longterm,
  title = {{Long-term follow-up results of topical imiquimod for high-grade cervical intraepithelial neoplasia in young women: an original research.}},
  author = {Jungmi Kim and Ju-Hyun Kim and Yaesol Kim and Rumie Lee and Hyeonji Choi and Dae-Yeon Kim},
  journal = {BMC women's health},
  year = {2026},
  month = aug,
  doi = {10.1186/s12905-026-04685-8},
  url = {https://europepmc.org/article/MED/43009930},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Long-term follow-up results of topical imiquimod for high-grade cervical intraepithelial neoplasia in young women: an original research.
AU  - Jungmi Kim
AU  - Ju-Hyun Kim
AU  - Yaesol Kim
AU  - Rumie Lee
AU  - Hyeonji Choi
AU  - Dae-Yeon Kim
PY  - 2026
DA  - 2026/08/14
JO  - BMC women's health
DO  - 10.1186/s12905-026-04685-8
UR  - https://europepmc.org/article/MED/43009930
AB  - Background  Cervical excisional treatment is associated with adverse obstetric outcomes. Although imiquimod has been explored as a conservative alternative in trials like TOPIC-3, its definitive role remains debated. We aimed to evaluate the long-term efficacy of a clinician-applied imiquimod strategy specifically in women aged under 35 years to verify its potential for fertility preservation.Methods  We conducted a retrospective, single-arm cohort study of nulliparous women aged under 35 years with Cervical Intraepithelial Neoplasia (CIN) 2 or 3 and no prior excisional therapy between October 2021 and March 2024. The primary outcomes were histological regression assessed immediately post-treatment (8 weeks) and during a prolonged follow-up period.Results  A total of 100 patients were included. The immediate regression rate following the 8-week imiquimod course was 96.0%, with an initial high risk Human Papillomavirus (hr-HPV) clearance rate of 57.1%. In the follow-up analysis, the sustained regression rate reached 91.0%, and the cumulative hr-HPV clearance rate rose to 70.5%. Notably, patients with CIN2 without HPV 16/18 achieved the highest regression rate (96.5%), successfully avoided or postponed surgical intervention.Conclusions  The clinician-applied imiquimod strategy offers a robust therapeutic impact, safely postponing surgical intervention for approximately one year in reproductive-aged women with CIN 2/3. This imiquimod strategy serves as an effective bridging therapy that preserves fertility without compromising clinical safety, providing a supportive clinical decision-making model for individualized non-surgical management.
SN  - 1472-6874
ER  -