The Value of HPV Testing for Cervical Cancer Screening in Women Living With HIV (PAPILLO-VIH)

Sponsor
Centre Hospitalier de Saint-Denis (Other)
Overall Status
Recruiting
CT.gov ID
NCT05968183
Collaborator
(none)
200
1
15
13.3

Study Details

Study Description

Brief Summary

The main objective of this study is to evaluate the interest of a screening strategy based on the HPV test in patients living with HIV, compared to the cell smear alone in the same population.

The Secondary objective of this study is to verify if the use of HPV testing could allow for a longer follow-up of these patients in case of negativity, and thus allow for a standardization of clinicians' practices.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Since 2019, a new screening strategy has been implemented and is based on high-risk, HPV tests, which, when negative, allow for spaced monitoring in the general population after age 30 (every 5 years instead of every 3 years.)

    These tests therefore allow for earlier detection of patients at risk but also for longer follow-up when they are negative.

    To our knowledge, there is currently no evaluation of HPV testing as part of routine screening in patients living with HIV.

    The recommendations for this population are based on the use of the cervico-vaginal smear with cytological analysis. The smear should be taken every year and surveillance may be repeated every 3 years. If there are 3 consecutive smears without abnormalities and a controlled viral load with CD4 counts > 500 mm3. In practice, many patients do not meet these criteria and must, therefore, undergo annual screening; the increase in the number of smears also leads to an increase in the number of second-line examinations such as colposcopy.

    Since there is no recommendation for HPV testing in this population, the use of dual detection (cytology and HPV testing) is left to the discretion of the clinician.

    By mutual agreement with the clinicians of the maternity department of the Saint-Denis Hospital (CHSD), this double detection was introduced in 2021, using the same sample (single swab for both analyses: cytology and HPV test).

    Therefore, it seems interesting to verify the possibility of a screening strategy based on HPV testing in patients living with HIV, by correlating the results of HPV testing and cell smears in the population of patients living with HIV.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Value of HPV Testing for Cervical Cancer Screening in Women Living With HIV
    Actual Study Start Date :
    Jul 1, 2023
    Anticipated Primary Completion Date :
    Jul 1, 2024
    Anticipated Study Completion Date :
    Oct 1, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Demographic characteristics [Day 1]

    2. HIV history [Day 1]

    3. medical history [Day 1]

    4. comorbidities [Day 1]

    5. clinical examination data [Day 1]

    Secondary Outcome Measures

    1. Results of HPV Cytology [Day 1]

    2. Results of cell smear [Day 1]

    3. Results of additional examinations prescribed [Day 1]

      Results of any additional examinations prescribed

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years to 65 Years
    Sexes Eligible for Study:
    Female
    Inclusion Criteria:
    • Women living with HIV

    • Age 25-65 years

    • Managed in the CHSD maternity ward: consultation or hospitalization

    • Having signed a consent form

    Exclusion Criteria:
    • Age ≤ 24 years, or ≥ 66 years

    • Women who are not HIV positive

    • Patients under legal protection (guardianship, curatorship)

    • Patients deprived of liberty

    • Patients not affiliated to a social security system

    • Refusal to participate in the research

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centre Hospitalier de Saint-Denis Saint-Denis France

    Sponsors and Collaborators

    • Centre Hospitalier de Saint-Denis

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Centre Hospitalier de Saint-Denis
    ClinicalTrials.gov Identifier:
    NCT05968183
    Other Study ID Numbers:
    • CHSD_0026_MATER
    • 2022-A01844-39
    First Posted:
    Aug 1, 2023
    Last Update Posted:
    Aug 1, 2023
    Last Verified:
    Jul 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Centre Hospitalier de Saint-Denis
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 1, 2023