Predicting Response In Cervical Intraepithelial Neoplasia to Topical Imiquimod Treatment
Recruiting now
Conditions studied: Cervical High Grade Squamous Intraepithelial Lesion, Cervical Intraepithelial Neoplasia Grade 2/3, CIN 2/3, Cervical Intraepithelial Neoplasia
In brief
Imiquimod is a good non-invasive treatment option for women with cervical high-grade squamous intraepithelial neoplasia (cHSIL), especially those with a possible (future) pregnancy wish. Complete response to imiquimod occurs in 55-73% of patients, however side-effects of imiquimod are common and can be extensive. Therefore, biomarkers which can predict response to imiquimod therapy are warranted, to increase therapy efficacy and to avoid side effects in patients who will not respond. This prospective, multi-center cohort study aims to validate the potential of immune related biomarkers to predict the clinical response of patients with primary cHSIL to imiquimod, aims to explore the value of these immune biomarkers in recurrent/residual cHSIL to predict treatment responses for imiquimod and aims to explore their potential in spontaneous regression of cHSIL (CIN2).
Key facts
- Study ID
- NCT05405270
- Run by
- Catharina Ziekenhuis Eindhoven
- People needed
- 410
- Starts
- 2022-06-01
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2023-09-11
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Primary cHSIL lesions (e.g. CIN3 or CIN 2), histologically confirmed by diagnostic biopsy Nota bene: In case of CIN 2, expectative management must be discussed according to the Dutch national guideline with the patient, if the patient prefers imiquimod therapy the patient can be treated with imiquimod and enrolled in the study, if the patient prefers expectative management they can be enrolled in the observational CIN 2 group.
- Recurrent or residual cHSIL lesions after initial LLETZ treatment (e.g. CIN2 or CIN3), histologically confirmed by diagnostic biopsy
- Age of 18 years or older
You may not qualify if…
- Concomitant diagnoses of VAIN (vaginal intraepithelial neoplasia e.g. vaginal HSIL)
- PAP (Papanicolaou) 4 cytology as indication for the baseline colposcopy at study entrance
- Adenocarcinoma in situ (AIS) diagnosis
- Previous imiquimod therapy for cHSIL
- Previous cervical malignancy
- Current malignant disease
- Immunodeficiency (including HIV/AIDS and immunosuppressive medication)
- Pregnancy
- Legal incapability
- Insufficient knowledge of the Dutch language
Where it is running
- Isala — Zwolle, Netherlands (enrolling)
- Albert Schweitzer Ziekenhuis — Dordrecht, Netherlands (enrolling)
- Catharina Ziekenhuis Eindhoven — Eindhoven, Netherlands (enrolling)
- Tergooi MC — Hilversum, Netherlands (enrolling)
- Medisch Centrum Leeuwarden — Leeuwarden, Netherlands (enrolling)
- Amphia — Breda, Netherlands (enrolling)
- Maastricht Universitair Medisch Centrum — Maastricht, Netherlands (enrolling)
- Radboudumc — Nijmegen, Netherlands (enrolling)
- Erasmus Medisch Centrum — Rotterdam, Netherlands (enrolling)
- Franciscus Gasthuis & Vlietland — Rotterdam, Netherlands (enrolling)
- HagaZiekenhuis — The Hague, Netherlands (enrolling)
- Diakonessenhuis — Utrecht, Netherlands (enrolling)
- Máxima MC — Veldhoven, Netherlands (enrolling)
- VieCuri Medisch Centrum — Venlo, Netherlands (enrolling)
- Leiden Universitair Medisch Centrum — Leiden, Netherlands
Full record on ClinicalTrials.gov
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