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NCT Number: NCT06713655

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

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Treatment failure rate within 24 months after surgery (cervical intraepithelial neoplasia grade 2+ (CIN2+) recurrence/residual rates)

    Time frame: 2 years post-surgery

    the percentage of HSIL treatment failure (CIN2+ recurrence and residual) within 24 months after surgery

  2. Sensitivity of the PAX1 methylation to detect treatment failure

    Time frame: 2 years post-surgery

  3. specificity of the PAX1 methylation to detect treatment failure

    Time frame: 2 years post-surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Lv Weiguo, Ph.D

CONTACT

[email protected]

86-13588819218

Sponsors and collaborators

Lead sponsor

Women's Hospital School Of Medicine Zhejiang University

Other

Collaborators

  • Huzhou Maternity and Child Care Hospital
  • Jiaxing Maternity and Child Health Care Hospital
  • Jinhua Central Hospital
  • Ningbo No. 1 Hospital
  • Shaoxing Maternity and Child Health Care Hospital
  • Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Dec 3, 2024
Registry last updated
Dec 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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