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RecruitingInterventional

The Effectiveness of Screening Women With Lower Genital Tract Neoplasia or Cancers for Anal Cancer Precursors

NCT ID: NCT05217940Sponsor: Icahn School of Medicine at Mount SinaiLast updated: 2025-08-22

Summary

The goal of this single arm trial is to prospectively evaluate screening methods for anal cancer precursors in HIV uninfected women with a history of lower genital tract neoplasias and cancers.

Detailed description

This single arm trial will enroll 300 HIV uninfected women with a history of genital neoplasia (ie., cervical intraepithelial neoplasia grade 2-3, vaginal intraepithelial neoplasia grade 2-3 or vulvar intraepithelial neoplasia grade 2-3) or early stage cervical or vulvar cancer to evaluate the test characteristics of anal cancer screening tests (cytology, HPV testing and high resolution anoscopy) and determine the prevalence and incidence of anal high-grade squamous intraepithelial lesions in this population. Participants will undergo evaluation at baseline and then at 12 and 24 months. The investigators will also measure the acceptability of anal cancer screening in this previously unstudied group. The trial is expected to run from 2021-2027.

Arms & interventions

  • Diagnostic TestDiagnostic tests for anal cancer screening

    The initial screening interventions will include the collection of (1) anal cytology; (2) self-collected HPV testing specimens (by subjects); (3) a clinician collected HPV specimen. A digital rectal exam will also be done on all patients.

Outcome measures

Primary

  • Sensitivity and specificity of anal cytology

    Test sensitivity and specificity

    Time frame: Baseline

Secondary

  • Concordance of self- and clinician-collected PCR testing

    Time frame: baseline

  • Prevalence of hrHPV types at baseline

    Time frame: Baseline

  • hrHPV with Cobas PCR testing (self-collected)

    Time frame: Baseline

  • hrHPV with Cobas PCR testing (self-collected)

    Time frame: 12 months

  • hrHPV with Cobas PCR testing (self-collected)

    Time frame: 24 months

  • hrHPV with Cobas PCR testing (clinician-collected)

    Time frame: Baseline

  • hrHPV with Cobas PCR testing (clinician-collected)

    Time frame: 12 months

  • hrHPV with Cobas PCR testing (clinician-collected)

    Time frame: 24 months

  • Prevalence of aHSIL at baseline

    Time frame: Baseline

  • Incidence of aHSIL at follow-up

    Time frame: 24 months

  • Screening Experience Survey

    Time frame: Baseline

  • Incidence of hrHPV, by type

    Time frame: 12 months

  • Incidence of hrHPV, by type

    Time frame: 24 months

  • Proportion of subjects with new hrHPV infection

    Time frame: 12 months

  • Proportion of subjects with new hrHPV infection

    Time frame: 24 months

Eligibility criteria

Sex: FemaleAge: 35 Years and olderHealthy volunteers: No
Inclusion Criteria: * Women with a history of pathologically proven high-grade genital HPV-associated neoplastic disease (cervical intraepithelial neoplasia 2+, vulvar intraepithelial neoplasia 2+, or vaginal intraepithelial neoplasia 2+, or history of non-metastatic cervical, vaginal or vulvar cancer) * Documented HIV seronegativity * Aged 35 years and older * Seen in the Mount Sinai Health System (MSHS) or the Harris Health System (HHS) in Houston * English or Spanish speaking Exclusion Criteria: • prior history or high resolution anoscopy

Study locations (3)

Icahn School of Medicine at Mount Sinai

New York, New York, 10029

Recruiting
Nadia M Zubair, MPH · Contact
Keith Sigel, MD PHD MPH · Principal Investigator

Medical University of South Carolina

Charleston, South Carolina, 29425

Recruiting
Ashish Deshmukh, PhD · Principal Investigator

University of Texas M D Anderson Cancer Center

Houston, Texas, 77030

Recruiting
Elizabeth Chiao · Contact
Elizabeth Chiao, MD · Principal Investigator