Anal Dysplasia Study of Men Who Have Sex With Men Living With HIV
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|ClinicalTrials.gov Identifier: NCT01663558|
Recruitment Status : Withdrawn (funding not available)
First Posted : August 13, 2012
Last Update Posted : August 22, 2016
Men who have sex with men (MSM) are at increased risk for HPV-related anal neoplasia and anal squamous cell carcinoma; concomitant HIV infection roughly doubles that risk.
- To compare the efficacy of ablative therapy to topical imiquimod therapy in the management of anal dysplasia in HIV-infected men.
- To describe relationship between cytologic grade of anal dysplasia (as reported on screening anal Pap test) and pathologic grade reported on anal mucosa histopathologic examination.
- To describe demographic, sexual practices, HPV-specific, and HIV-specific correlates of anal dysplasia.
- To describe adverse effects associated with ablative therapy and topical imiquimod therapy.
Prospective, randomized controlled clinical trial. This will be a pilot study. All subjects will undergo baseline anal Pap, HRA with biopsies as indicated, and anal HPV testing. If AIN 2 or 3 is discovered on histopathologic examination, subject will be offered observation only or treatment. If he chooses treatment, he will be randomized to: 1) imiquimod anal suppositories three times weekly for 3 months, or 2) appropriate ablative therapy as determined by colorectal surgeon. During imiquimod treatment (not applicable to ablative group as their treatment will be completed in one visit) subjects will be followed for 2 weeks, 4 weeks, 8 weeks, and 12 weeks with anal Pap, HRA with biopsies as indicated, and anal HPV testing. After therapy completed in each treatment group, subjects will be followed for 1 month, 3 months, 6 months, 9 months, and 12 months post-therapy with anal Pap, HRA with biopsies as indicated, and anal HPV testing. Observation only subjects will be evaluated every 3 months with anal Pap, HRA with biopsies as indicated, and anal HPV testing for 12 months. We have chosen a goal of 30 subjects in each treatment group and 10 subjects in the observation only group based on the likelihood of enrolling a study of this type in a reasonable amount of time.
Main Outcome Measures:
- Anal Pap cytologic grade, including regression and recurrence during course of study
- HPV type in anal canal, including regression and recurrence during course of study
- Anal histology, including regression and recurrence during course of study
- Adverse effects experienced during treatment, recorded in symptom log
|Condition or disease||Intervention/treatment||Phase|
|Anal Dysplasia Human Papilloma Virus HIV||Drug: imiquimod Procedure: ablative||Phase 4|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Anal Dysplasia Study of Men Who Have Sex With Men Living With HIV|
|Study Start Date :||May 2015|
|Estimated Primary Completion Date :||December 2015|
|Estimated Study Completion Date :||May 2016|
Active Comparator: imiquimod
i. Each subject will use an imiquimod anal suppository three times weekly (overnight on Monday, Wednesday, Friday) for 12 weeks.
ii. Each subject will be asked to abstain from receptive anal sex during therapy period (12 weeks).
iii. If local imiquimod adverse effects are severe, a 7-day period off of treatment will be permitted.
iv. During 12 week therapy period, each subject will be evaluated 2, 4, 8, and 12 weeks after starting therapy. At each visit, subject will complete a therapy questionnaire and undergo anal Pap, HRA with biopsies as indicated, and anal HPV testing.
v. After therapy completed (12 weeks), subject will enter 12 month observation period.
Other Name: Aldara
Active Comparator: ablative
i. Subject will be referred to colorectal surgeon, will complete a therapy questionnaire, and will be treated in accordance with treatment algorithm which is already in use.
ii. Subject will be asked to abstain from receptive anal sex for 12 weeks after ablative therapy.
iii. After therapy, subject will enter 12 month observation period.
No Intervention: Observation
i. Given lack of accepted guidelines and outcome data on dysplasia management, the study PI will thoroughly discuss risks and benefits of observation/monitoring and treatment of dysplasia.
ii. If treatment is chosen, subject will be randomized to 1) ablative group, or 2) imiquimod group and begin therapy. Observation subjects will continue observation visits (observation questionnaire, anal Pap, HRA with biopsies as indicated, and anal HPV testing) every 3 months for 12 months (4 additional study visits).
- cytologic grade [ Time Frame: 3 months ]Anal Pap cytologic grade, including regression and recurrence during course of study
- HPV [ Time Frame: 3 months ]HPV type in anal canal, including regression and recurrence during course of study
- histologic grade [ Time Frame: 3 months ]Anal histology, including regression and recurrence during course of study
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01663558
|United States, California|
|San Diego, California, United States, 92134|
|Principal Investigator:||John D Malone, MD||United States Naval Medical Center, San Diego|