Clinical Trial Evaluating Secondary HPV Vaccination After Treatment of High-grade Cervical Lesions

NCT ID: NCT06658405

Last Updated: 2025-09-26

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 85 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-01-13
• Study Completion Date: 2031-10-31

Brief Summary

This is a single-center, Phase II interventional study evaluating secondary HPV vaccination after treatment of high-grade cervical lesions. The study aims to estimate the rate of HPV clearance within two years following an initial positive HPV control test in women over 45 years of age who are chronic HPV carriers and have undergone treatment for high-grade intraepithelial cervical lesions, and who receive HPV vaccination.

The study includes two cohorts:

1. Eligible patients who consent to vaccination will participate in a prospective, single-center, single-arm, interventional clinical trial (Category 2).

2. Non-vaccinated patients will be included in a non-interventional observational study, with no changes to their standard care.

Detailed Description

The aim of this study is to estimate the proportion of HPV clearance within two years following an initial positive HPV control test in women over 45 years old who are chronic HPV carriers and have undergone treatment for high-grade intraepithelial cervical lesions. These women will receive HPV vaccination as part of the study.

Other objectives of the study include:

1. Describing the dynamics of viral clearance in chronic HPV carriers who receive HPV vaccination.

2. Evaluating the safety of HPV vaccination.

3. Estimating the incidence of recurrence of high-grade intraepithelial cervical lesions in chronic HPV carriers after surgical treatment of the initial lesion and HPV vaccination.

4. Estimating the incidence of invasive gynecological cancers (cervical, vaginal, or vulvar) in chronic HPV carriers after surgical treatment of the initial lesion and HPV vaccination.

5. Identifying factors associated with the refusal of HPV vaccination, such as smoking, parity, body mass index, employment status, education level, family history, and marital status.

6. Describing compliance with the proposed vaccination schedule in terms of:

1. Number of injections completed.

2. Adherence to the timing of injections.

7. Evaluating the effect of vaccination on:

1. HPV clearance within two years.

2. The dynamics of viral clearance.

3. The risk of recurrence of high-grade intraepithelial lesions.

4. The risk of developing invasive gynecological cancers (cervical, vaginal, or vulvar).

by comparing vaccinated patients included in the clinical trial with the cohort of non-vaccinated patients (those who refused HPV vaccination or for other reasons).

Conditions

Cervical Lesion

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Vaccinated patients

Human papillomavirus vaccine, nonvalent, Gardasil 9

Group Type: EXPERIMENTAL

Human Papillomavirus 9-valent Vaccine, Recombinant

Intervention Type: BIOLOGICAL

HPV vaccine administered in three doses: first dose on day 1, second dose 2 months later, and third dose 4 months after the second dose, within a one-year period.

Non-vaccinated patients

no changes to standard care

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Human Papillomavirus 9-valent Vaccine, Recombinant

HPV vaccine administered in three doses: first dose on day 1, second dose 2 months later, and third dose 4 months after the second dose, within a one-year period.

Intervention Type: BIOLOGICAL

Other Intervention Names

Gardasil 9

Eligibility Criteria

Inclusion Criteria

1. Common eligibility criteria for the study (for both cohorts) :

1. Female patient over 45 years old

2. Patient treated by conization for high-grade cervical epithelial lesion

3. Positive HPV test at the 6-month post-operative control (a delay of 6 to 12 months will be accepted), leading to an indication for a control colposcopy (+/- biopsy) according to standard surveillance practices.

4. N.B. : Patients with abnormalities at the initial control colposcopy and/or positive biopsy remain eligible for the study, whether vaccinated or not.

2. Additional eligibility criteria for the clinical trial (Vaccinated patients cohort)

1. No contraindication to HPV vaccination with Gardasil 9

2. Patient consented to HPV vaccination with Gardasil 9

3. Affiliated with a social security system

4. Informed and signed written consent provided

5. N.B. : Patients infected with HIV are eligible for the vaccine trial provided they are on antiretroviral therapy.

1. Patient eligible for the study (a) and not eligible for the clinical trial (b) due to:

• refusal of vaccination, or
• A contraindication to vaccination

2. No objection to the use of their personal data for research purposes

N.B. : A patient who initially refused vaccination may later request to be vaccinated as part of the trial after signing the consent form. The vaccine trial analysis will include all patients who started vaccination within 6 months after the initial HPV control test.

Exclusion Criteria

1. History of primary HPV vaccination

2. History of HPV-induced invasive cancer (cervical, vaginal, vulvar, anal, oropharyngeal cancer)

1. Patient refusing HPV vaccination

2. Patient with a contraindication to HPV vaccination with Gardasil 9

3. Patient deprived of liberty or under guardianship

• Minimum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Canceropôle Nord Ouest

OTHER

Sponsor Role: collaborator

Centre Oscar Lambret

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Nora ALLOY, MD

Role: STUDY_DIRECTOR

Centre Oscar Lambret

Locations

Centre Oscar Lambret

Lille, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Emilie HEYMAN-DECOUPIGNY

Role: CONTACT

promotion@o-lambret.fr

0320295918

Hugo JOSE

Role: CONTACT

promotion@o-lambret.fr

0320295918

Facility Contacts

Nora ALLOY, MD

Role: primary

n-alloy@o-lambret.fr

0320295959

Other Identifiers

2024-513081-19-00

Identifier Type: CTIS

Identifier Source: secondary_id

HPV2-2303

Identifier Type: -

Identifier Source: org_study_id