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Human Papillomavirus Infection and Related Anal Lesions in HIV-positive Men Who Have Sex With Men (APACHES)

Primary Purpose

Hiv Infection

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Standard proctologic examination
High resolution anoscopy
Biopsy(ies) during High Resolution Anoscopy
High Resolution Anoscopy biannually
Sponsored by
ANRS, Emerging Infectious Diseases
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Hiv Infection

Eligibility Criteria

35 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Men who have sex with men
  • At least 35 years old
  • HIV-positive (documented search of HIV infection, with HIV status determined according to HAS algorithm)
  • Signed informed consent
  • Affiliated to or beneficiary of French social security
  • All severity criteria and evolution of HIV disease are accepted (including AIDS stage and co-infections)

Exclusion Criteria:

  • Contraindication to biopsy
  • History of anal cancer or pelvic radiotherapy
  • AIN2/3 treated during previous year
  • Current anticancer chemotherapy or within 24 months before inclusion
  • Difficulty in evaluation (anus reshaped and/or scarred)
  • Individual placed under judicial protection
  • Foreseen absence which may hamper participation; insufficient motivation; associated pathology with priority for care

Sites / Locations

  • Diaconesses

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Subjects

Arm Description

Standard proctologic examination with digital rectal examination and 2 anal swabs at initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits High resolution anoscopy at initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits Biopsy(ies) during High Resolution Anoscopy only if lesion suggestive of AIN detected during High Resolution Anoscopy High Resolution Anoscopy biannually only if high-grade lesion (ASC-H, HSIL ou AIN2/3)

Outcomes

Primary Outcome Measures

Evaluation of high-grade anal lesions by high resolution anoscopy
Evaluation of anal HPV infection by DNA, RNA and protein detection
Quantification of spontaneous regression of high-grade anal lesions

Secondary Outcome Measures

Evaluation of anal HPV infection by DNA, RNA and protein detection
Evaluation of anal HPV infection by DNA, RNA and protein detection
Evaluation of anal HPV infection by DNA, RNA and protein detection
Evaluation of anal HPV infection by DNA, RNA and protein detection

Full Information

First Posted
October 15, 2014
Last Updated
December 4, 2020
Sponsor
ANRS, Emerging Infectious Diseases
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1. Study Identification

Unique Protocol Identification Number
NCT02287961
Brief Title
Human Papillomavirus Infection and Related Anal Lesions in HIV-positive Men Who Have Sex With Men
Acronym
APACHES
Official Title
Natural History of Anal Human Papillomavirus Infection and Associated Disease in HIV-infected Men Who Have Sex With Men: Towards an Evidence Base for the Prevention of Anal Cancer.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 2014 (Actual)
Primary Completion Date
June 2021 (Anticipated)
Study Completion Date
June 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ANRS, Emerging Infectious Diseases

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Multicentric epidemiological non-comparative study in France characterising evolution of anal Human papillomavirus (HPV) infection and related lesions and evaluating markers associated with the observed evolution. Estimated enrolment: 500 Principal Outcomes Detection of high-grade cytological and histological anal lesions by high resolution anoscopy Spontaneous regression of high-grade anal lesions Detection of anal HPV infection Intervention (procedure): Patient medical interview (initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits) Standard proctologic examination with digital rectal examination and 2 anal swabs (initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits) High resolution anoscopy (initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits) Only if lesion suggestive of Anal Intraepithelial Neoplasia (AIN) detected during High Resolution Anoscopy (HRA): - anal biopsy(ies) during HRA Only if high-grade lesion: - HRA biannually
Detailed Description
Intervention (procedure): Patient medical interview (initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits) Standard proctologic examination with digital rectal examination and 2 anal swabs (initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits) High resolution anoscopy (initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits) Only if lesion suggestive of Anal Intraepithelial Neoplasia (AIN) detected during High Resolution Anoscopy (HRA): - anal biopsy(ies) during HRA Only if high-grade lesion (Atypical squamous cells-cannot exclude high-grade squamous intraepithelial lesion (ASC-H), High grade Superficial Intra-epithelial Lesion (HSIL) or AIN2/3): - HRA biannually

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hiv Infection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Subjects
Arm Type
Other
Arm Description
Standard proctologic examination with digital rectal examination and 2 anal swabs at initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits High resolution anoscopy at initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits Biopsy(ies) during High Resolution Anoscopy only if lesion suggestive of AIN detected during High Resolution Anoscopy High Resolution Anoscopy biannually only if high-grade lesion (ASC-H, HSIL ou AIN2/3)
Intervention Type
Procedure
Intervention Name(s)
Standard proctologic examination
Intervention Description
(with digital rectal examination and 2 anal swabs) at initial inclusion visit, M12 and M24 follow-up visits and if applicable M6 and M18 control visits
Intervention Type
Procedure
Intervention Name(s)
High resolution anoscopy
Intervention Description
at initial inclusion visit, Month 12 and Month 24 follow-up visits and if applicable Month 6 and Month 18 control visits
Intervention Type
Procedure
Intervention Name(s)
Biopsy(ies) during High Resolution Anoscopy
Intervention Description
only if lesion suggestive of AIN detected during High Resolution Anoscopy
Intervention Type
Procedure
Intervention Name(s)
High Resolution Anoscopy biannually
Intervention Description
Only if high-grade lesion (ASC-H, HSIL ou AIN2/3)
Primary Outcome Measure Information:
Title
Evaluation of high-grade anal lesions by high resolution anoscopy
Time Frame
Initial inclusion visit
Title
Evaluation of anal HPV infection by DNA, RNA and protein detection
Time Frame
Initial inclusion visit
Title
Quantification of spontaneous regression of high-grade anal lesions
Time Frame
Month 24
Secondary Outcome Measure Information:
Title
Evaluation of anal HPV infection by DNA, RNA and protein detection
Time Frame
Month 6
Title
Evaluation of anal HPV infection by DNA, RNA and protein detection
Time Frame
Month 12
Title
Evaluation of anal HPV infection by DNA, RNA and protein detection
Time Frame
Month 18
Title
Evaluation of anal HPV infection by DNA, RNA and protein detection
Time Frame
Month 24

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men who have sex with men At least 35 years old HIV-positive (documented search of HIV infection, with HIV status determined according to HAS algorithm) Signed informed consent Affiliated to or beneficiary of French social security All severity criteria and evolution of HIV disease are accepted (including AIDS stage and co-infections) Exclusion Criteria: Contraindication to biopsy History of anal cancer or pelvic radiotherapy AIN2/3 treated during previous year Current anticancer chemotherapy or within 24 months before inclusion Difficulty in evaluation (anus reshaped and/or scarred) Individual placed under judicial protection Foreseen absence which may hamper participation; insufficient motivation; associated pathology with priority for care
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isabelle Etienney
Organizational Affiliation
Hôpital Diaconesses Paris
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gary Clifford
Organizational Affiliation
International Agency for Research on Cancer
Official's Role
Study Director
Facility Information:
Facility Name
Diaconesses
City
Paris
Country
France

12. IPD Sharing Statement

Links:
URL
http://anrs.fr
Description
Agence nationale de recherches sur le sida et les hépatites virales (ANRS)

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Human Papillomavirus Infection and Related Anal Lesions in HIV-positive Men Who Have Sex With Men

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