Tolerability, Safety, & Efficacy of Argon Plasma Coagulation to Treat Anal Intraepithelial Neoplasia in HIV-Positive Men
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|ClinicalTrials.gov Identifier: NCT00428285|
Recruitment Status : Completed
First Posted : January 29, 2007
Last Update Posted : August 1, 2016
|Condition or disease||Intervention/treatment||Phase|
|Anus Neoplasms HIV Infections||Procedure: Argon Plasma Coagulation||Phase 2|
HIV infected men having sex with men (MSM) are at increased risk of developing anal cancer compared to the general population and the incidence continues to increase despite better control of HIV infection with HAART (Highly Active Anti-Retroviral Therapy). The causative agent is known to be Human Papilloma Virus infection which can lead to dysplastic changes in the anus, detectable by High Resolution Anoscopy with biopsies. The analysis of the abnormal tissue can then be graded as Anal Intraepithelial Neoplasia 1 to 3, with AIN 2 or 3 considered as high grade dysplasia. These lesions are cancer precursors, but the proportion of lesions progressing to invasive anal cancer and the time to event are unknown. There is currently no recognized treatment to offer as standard of care although it is of general belief that treating these lesions, as it is done for women with CIN 2 and 3 (Cervical Intraepithelial Neoplasia) could help decrease the number of progressions to invasive anal cancer in MSM infected with HIV.
By experience at our center and results of this technique for other gastrointestinal pathologies, we believe Argon Plasma Coagulation (APC) could be a safe, well tolerated and efficient treatment of high-grade dysplasia (AIN 2/3) in HIV infected MSM.
This study will assess the APC treatment in 20 patients, all HIV infected MSM, with established AIN 2/3 (as confirmed with their last two anal biopsies, at least 4 months apart). Patients will then be followed with regular High Resolution Anoscopies for two years. The primary objective is to assess if APC is a safe and well tolerated treatment method for AIN 2/3 in HIV-positive MSM. As secondary objectives, the efficacy of APC treatment on AIN 2/3 lesions in HIV-positive MSM, the number of treatments with APC necessary to obtain regression or resolution of AIN 2/3 over two years and the efficacy of APC treatment to decrease anal HPV in this population will also be addressed.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||20 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase II, Prospective, Open-label, Pilot Study of the Tolerability, Safety, and Efficacy of Argon Plasma Coagulation for the Treatment of Anal Intraepithelial Neoplasia Grade 2 or 3 in HIV-positive Men Having Sex With Men|
|Study Start Date :||February 2007|
|Actual Primary Completion Date :||February 2010|
|Actual Study Completion Date :||July 2016|
|Experimental: Single Arm||
Procedure: Argon Plasma Coagulation
Argon Plasma Coagulation (APC) is a non-contact electrosurgical technique delivering a high-frequency electrical current through ionized argon gas i.e. the argon plasma. This current produces a zone of coagulation, desiccation, and devitalisation 2-3 mm deep. Patients will be offered up to 3 treatments if recurrence occur after the first two.
- High grade dysplasia (AIN 2/3) [ Time Frame: at 1 and 2 years ]
- Anal human papilloma virus (HPV) [ Time Frame: at 1 and 2 years ]
- Tolerability and safety of the treatment [ Time Frame: 2 years ]
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): NCT00428285
|Notre-Dame Hospital (Centre Hospitalier de l'Université de Montréal)|
|Montreal, Quebec, Canada, H2L 4M1|
|Royal Victoria Hospital (McGill University Health Center)|
|Montreal, Quebec, Canada, H2X 2P4|
|Principal Investigator:||Alexandra de Pokomandy, MD||Centre hospitalier de l'Université de Montréal (CHUM)|
|Principal Investigator:||George Ghattas, MD||McGill University Health Center and Centre Hospitalier de l'Université de Montréal (CHUM)|