Tolerability, Safety, & Efficacy of Argon Plasma Coagulation to Treat Anal Intraepithelial Neoplasia in HIV-Positive Men
Primary Purpose
Anus Neoplasms, HIV Infections
Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Argon Plasma Coagulation
Sponsored by
About this trial
This is an interventional treatment trial for Anus Neoplasms focused on measuring Human Papilloma Virus, HIV infected MSM, Treatment Experienced, Treatment Naive, Anal Intraepithelial Neoplasia
Eligibility Criteria
Inclusion Criteria:
- Age 18-65 years
- The last two High Resolution Anoscopies (HRA) of the patient, occurring at least 4 months apart, revealed histologic diagnoses of AIN 2 or 3
- HIV infected for at least 6 months
- Patient must be a man having sex with other men (currently or anteriorly).
- Able to provide a signed and dated Research Ethics Board (REB)-approved informed consent form (ICF) for the study
Exclusion Criteria:
- History of invasive anal cancer
- International normalized ratio (INR) > 1.5
- Platelet count < 50,000
- Previously (or currently) received chemotherapy or radiotherapy for AIN or anal cancer
- Currently receiving interferon or cidofovir treatment
- Diagnosed with circumferential (diffuse) high-grade AIN, or involving > 75% of the anal canal.
Sites / Locations
- Notre-Dame Hospital (Centre Hospitalier de l'Université de Montréal)
- Royal Victoria Hospital (McGill University Health Center)
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Single Arm
Arm Description
Outcomes
Primary Outcome Measures
High grade dysplasia (AIN 2/3)
Secondary Outcome Measures
Anal human papilloma virus (HPV)
Tolerability and safety of the treatment
Full Information
NCT ID
NCT00428285
First Posted
January 25, 2007
Last Updated
April 29, 2019
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
McGill University Health Centre/Research Institute of the McGill University Health Centre, CIHR Canadian HIV Trials Network
1. Study Identification
Unique Protocol Identification Number
NCT00428285
Brief Title
Tolerability, Safety, & Efficacy of Argon Plasma Coagulation to Treat Anal Intraepithelial Neoplasia in HIV-Positive Men
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 Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
July 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
McGill University Health Centre/Research Institute of the McGill University Health Centre, CIHR Canadian HIV Trials Network
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to assess if argon plasma coagulation (APC) is a safe and well tolerated treatment method for anal intraepithelial neoplasia (AIN) grade 2/3 in HIV-positive men having sex with men (MSM).
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anus Neoplasms, HIV Infections
Keywords
Human Papilloma Virus, HIV infected MSM, Treatment Experienced, Treatment Naive, Anal Intraepithelial Neoplasia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single Arm
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Argon Plasma Coagulation
Intervention Description
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.
Primary Outcome Measure Information:
Title
High grade dysplasia (AIN 2/3)
Time Frame
at 1 and 2 years
Secondary Outcome Measure Information:
Title
Anal human papilloma virus (HPV)
Time Frame
at 1 and 2 years
Title
Tolerability and safety of the treatment
Time Frame
2 years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18-65 years
The last two High Resolution Anoscopies (HRA) of the patient, occurring at least 4 months apart, revealed histologic diagnoses of AIN 2 or 3
HIV infected for at least 6 months
Patient must be a man having sex with other men (currently or anteriorly).
Able to provide a signed and dated Research Ethics Board (REB)-approved informed consent form (ICF) for the study
Exclusion Criteria:
History of invasive anal cancer
International normalized ratio (INR) > 1.5
Platelet count < 50,000
Previously (or currently) received chemotherapy or radiotherapy for AIN or anal cancer
Currently receiving interferon or cidofovir treatment
Diagnosed with circumferential (diffuse) high-grade AIN, or involving > 75% of the anal canal.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandra de Pokomandy, MD
Organizational Affiliation
Centre hospitalier de l'Université de Montréal (CHUM)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
George Ghattas, MD
Organizational Affiliation
McGill University Health Center and Centre Hospitalier de l'Université de Montréal (CHUM)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Notre-Dame Hospital (Centre Hospitalier de l'Université de Montréal)
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H2L 4M1
Country
Canada
Facility Name
Royal Victoria Hospital (McGill University Health Center)
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H2X 2P4
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
28833949
Citation
de Pokomandy A, Rouleau D, Lalonde R, Beauvais C, de Castro C, Coutlee F; Human Immunodeficiency and Papilloma Virus Research Group (HIPVIRG) Study Group. Argon plasma coagulation treatment of anal high-grade squamous intraepithelial lesions in men who have sex with men living with HIV: results of a 2-year prospective pilot study. HIV Med. 2018 Feb;19(2):81-89. doi: 10.1111/hiv.12544. Epub 2017 Aug 23.
Results Reference
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Tolerability, Safety, & Efficacy of Argon Plasma Coagulation to Treat Anal Intraepithelial Neoplasia in HIV-Positive Men
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