The Effectiveness of Screening Women With Lower Genital Tract Neoplasia or Cancers for Anal Cancer Precursors
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
Study locations (3)
Icahn School of Medicine at Mount Sinai
New York, New York, 10029
Medical University of South Carolina
Charleston, South Carolina, 29425
University of Texas M D Anderson Cancer Center
Houston, Texas, 77030