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Predicting Treatment Failure in HSIL Patients with Positive Margins After Conization Via Detection of PAX1 Methylation

Multicenter Study on PAX1 Methylation for Predicting Lesion Persistence/Recurrence in HSIL Patients with Positive Margins After Cervical Conization

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06713655
Enrollment
800
Registered
2024-12-03
Start date
2024-12-31
Completion date
2028-07-31
Last updated
2024-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Conization, High-grade Squamous Intraepithelial Lesions (HSIL)

Keywords

cervical intraepithelial neoplasia, conization, positive margins, cervical cancer, treatment failure, residual/recurrent disease

Brief summary

The goal of this multicenter, observational study is to evaluate whether methylation testing of paired box gene 1 (PAX1) can better predict and diagnose recurrence or persistent disease in patients with positive margins after cervical conization for high-grade squamous intraepithelial lesion (HSIL). The main question it aims to answer is: Can PAX1 gene methylation testing provide a more accurate and effective prediction and diagnosis of cervical disease recurrence/persistence in addition to existing methods? Participants will be managed according to the latest clinical guidelines, and during follow-up, a non-invasive test, PAX1 gene methylation testing, will be added.

Detailed description

This study is a multicenter, prospective observational study that qualitatively assesses the methylation status of the PAX1 gene in cervical exfoliated cells from patients with HSIL and positive margins after conization. The aim is to evaluate the ability of PAX1 gene methylation testing to predict treatment failure (lesion recurrence or persistence). The first follow-up occurs 6 months post-surgery, including high-risk human papillomavirus (hrHPV) testing and cytology, with referral for colposcopy, including biopsy and/or endocervical curettage (ECC), if necessary. Subsequent management and follow-up are based on examination results, following clinical guidelines, and arranged at intervals of 6-12 months depending on the findings. The follow-up includes routine clinical examinations widely applied in practice, and PAX1 testing will be completed at each follow-up visit. PAX1 testing, like hrHPV testing and cytology, will be performed using cervical exfoliated cells.

Interventions

None listed

Sponsors

Huzhou Maternity and Child Care Hospital
CollaboratorUNKNOWN
Jiaxing Maternity and Child Health Care Hospital
CollaboratorOTHER
Shaoxing Maternity and Child Health Care Hospital
CollaboratorOTHER
Ningbo No. 1 Hospital
CollaboratorOTHER
Jinhua Central Hospital
CollaboratorOTHER
Taizhou Hospital Zhejiang Province
CollaboratorUNKNOWN
Women's Hospital School Of Medicine Zhejiang University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
26 Years to 54 Years
Healthy volunteers
No

Inclusion criteria

* Age greater than 25 years and less than 55 years; * First-time cervical conization (cold knife conization or loop electrosurgical excision procedure); * Postoperative pathology showing HSIL (CIN2 or CIN3); * Positive margins for HSIL (CIN2 or CIN3) in conization specimen.

Exclusion criteria

* The presence of other malignant tumors or precancerous lesions; * Lack of willingness for follow-up; * Pregnant or breastfeeding women; * Unable or unwilling to complete follow-up examinations; * History of prior cervical disease treatment (surgical or physical therapy); * Presence of immune system disorders.

Design outcomes

Primary

MeasureTime frameDescription
Treatment failure rate within 24 months after surgery (cervical intraepithelial neoplasia grade 2+ (CIN2+) recurrence/residual rates)2 years post-surgerythe percentage of HSIL treatment failure (CIN2+ recurrence and residual) within 24 months after surgery
Sensitivity of the PAX1 methylation to detect treatment failure2 years post-surgery
specificity of the PAX1 methylation to detect treatment failure2 years post-surgery

Countries

China

Contacts

Primary ContactLv Weiguo, Ph.D
lbwg@zju.edu.cn86-13588819218

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026