Screening for Anal Cancer in Women With High-grade Vulvar Dysplasia or Vulvar Cancer. (NCT03061435)
๐ฉบ Plain-English Summary (8th-Grade Level)
Almost half of all women will develop an HPV infection in their lifetime. While most infections are naturally asymptomatic or cleared by the immune system, some persist and can lead to the development of cervical, vulvar, or anal lesions and eventually cancer. Screening regimens for these lesions are currently only in place for the cervix through regular Pap tests. These Pap tests usually involve an examination of the vulva -however, no screening procedures exist for anal cancer for women. Several studies have suggested that women with existing gynecological lesions are more likely to develop anal lesions and anal cancer. Here the investigators propose a multi-center study which seeks to screen for and treat anal cancer in women over the age of 40 with vulvar lesions and a stable immune system. The investigators will achieve this through performing anal Pap smears on eligible women and conducting High Resolution Anoscopy (HRA) and appropriate treatment procedures on those with abnormal anal cells. With enough evidence, there may be an indication to establish regular anal cancer screening measures in this potentially underserved population. Hypothesis: The investigators hypothesize that at least 40% of women with vulvar cancer or VIN2/3 will have abnormal anal cytology. 35% of the population will be hrHPV DNA positive and 11% will additionally have AIN2/3. This prospective study may lay the groundwork for routine anal screening regimens in Ontario and help shift health policy to treat this population.
Who can join: Review the eligibility criteria below.
Location: Odette Cancer Centre โ Toronto, Ontario
Age range: 40 Years
๐งช Interventions in This Study
- Screening anal Pap smear - No high-resolution anoscopy (PROCEDURE)
- Screening anal Pap smear - High-resolution anoscopy (PROCEDURE)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Odette Cancer Centre โ Toronto, Ontario
๐ Contact the Study Coordinator
Phone: (416) 480-5000
Email: nithla.mohanathas@sunnybrook.ca
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Vulvar Cancer
- Study of Near-Infrared Imaging With Indocyanine Green for Detection of Sentinel Lymph Nodes in People With Vulvar Cancer โ Basking Ridge, New Jersey
- Cisplatin+Pembrolizumab+RT in Vulvar Cancer โ Boston, Massachusetts
- STRatIfication of Vulvar Squamous Cell Carcinoma by HPV and p53 Status to Guide Excision โ Vancouver, British Columbia
- Indocyanine Green for Detection of Sentinel Lymph Nodes In Comparison to ICG Plus Technetium in the Evaluation of Vulvar Squamous Cell Carcinoma โ Hamilton, Ontario
- Groningen International Study on Sentinel Nodes in Vulvar Cancer-III โ Orange, California
Explore by condition: All Vulvar Cancer clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.