The rate of anal carcinoma among HIV positive men is 70/100,000 person years. This is higher than the rate of cervical carcinoma prior to the onset of routine cytology screening. Anal squamous intra-epithelial lesions (ASIL) are pre-malignant lesions that can be found by screening cytology analogous to cervical dysplasia. It is felt that persistent infection with oncogenic subtypes of human papillomavirus (HPV) is the most important cofactor for development of anal carcinoma. Prior to the routine use of highly active anti-retroviral therapy, screening for anal dysplasia was studied in large cohorts of predominantly white HIV+ and HIV- men who have sex with men. High rates of ASIL and anal infection with HPV were found. It is not clear how this applies to other groups of HIV+ men including minorities, heterosexual men, and intravenous drug users, and how the rate of HPV and anal dysplasia may have changed after widespread use of HAART. This study will enroll 350 HIV+ men and 200 HIV- men who are 40% Hispanic and 40% African-American. Forty percent of the HIV+ men will report intravenous drug use or sex with women as their risk behavior for HIV. A standardized questionnaire will be administered to determine past sexual behaviors. Each participant will undergo anal cytology and anal HPV testing. Those individuals with oncogenic HPV at the first test will be followed with anal cytology and HPV testing every six months for a total of two years or five exams. Each participant with abnormal cytology will undergo high-resolution anoscopy with biopsy. Factors associated with prevalent ASIL and HPV infection including immunologic and sexual parameters will be compared using logistic regression. Persistence of HPV will be defined as the time to the first negative test for HPV and will be analyzed using Cox proportional hazards model. Factors associated with persistence will be included in a multiple Cox model. The influence of HAART will be assessed in both the prevalence and prospective components by including a term in the multiple models for length of time on anti-retroviral therapy with suppression of HIV. This study will help provide important new information on which groups of HIV+ men may benefit from screening and how HAART may modify this risk.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Mentored Patient-Oriented Research Career Development Award (K23)
Project #
1K23AI055038-01
Application #
6613543
Study Section
Acquired Immunodeficiency Syndrome Research Review Committee (AIDS)
Program Officer
Ruiz, Monica S
Project Start
2002-09-01
Project End
2007-05-31
Budget Start
2002-09-01
Budget End
2003-05-31
Support Year
1
Fiscal Year
2002
Total Cost
$130,680
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Ellsworth, G B; Lensing, S Y; Ogilvie, C B et al. (2018) A delayed dose of quadrivalent human papillomavirus vaccine demonstrates immune memory in HIV-1-infected men. Papillomavirus Res 6:11-14
Megill, Christina; Wilkin, Timothy (2017) Topical therapies for the treatment of anal high-grade squamous intraepithelial lesions. Semin Colon Rectal Surg 28:86-90
Wilkin, Timothy; Lee, Jeannette Y; Lensing, Shelly Y et al. (2013) High-grade anal intraepithelial neoplasia among HIV-1-infected men screening for a multicenter clinical trial of a human papillomavirus vaccine. HIV Clin Trials 14:75-9
Wilkin, Timothy J; Goetz, Mathew Bidwell; Leduc, Robert et al. (2011) Reanalysis of coreceptor tropism in HIV-1-infected adults using a phenotypic assay with enhanced sensitivity. Clin Infect Dis 52:925-8
Wilkin, Timothy J; Su, Zhaohui; Krambrink, Amy et al. (2010) Three-year safety and efficacy of vicriviroc, a CCR5 antagonist, in HIV-1-infected treatment-experienced patients. J Acquir Immune Defic Syndr 54:470-6
Wilkin, Timothy; Lee, Jeannette Y; Lensing, Shelly Y et al. (2010) Safety and immunogenicity of the quadrivalent human papillomavirus vaccine in HIV-1-infected men. J Infect Dis 202:1246-53
Tsibris, Athe M N; Paredes, Roger; Chadburn, Amy et al. (2009) Lymphoma diagnosis and plasma Epstein-Barr virus load during vicriviroc therapy: results of the AIDS Clinical Trials Group A5211. Clin Infect Dis 48:642-9
Su, Zhaohui; Gulick, Roy M; Krambrink, Amy et al. (2009) Response to vicriviroc in treatment-experienced subjects, as determined by an enhanced-sensitivity coreceptor tropism assay: reanalysis of AIDS clinical trials group A5211. J Infect Dis 200:1724-8
Wilkin, Timothy J; McKinnon, John E; DiRienzo, A Gregory et al. (2009) Regimen simplification to atazanavir-ritonavir alone as maintenance antiretroviral therapy: final 48-week clinical and virologic outcomes. J Infect Dis 199:866-71
Wilkin, Timothy J; Su, Zhaohui; Kuritzkes, Daniel R et al. (2007) HIV type 1 chemokine coreceptor use among antiretroviral-experienced patients screened for a clinical trial of a CCR5 inhibitor: AIDS Clinical Trial Group A5211. Clin Infect Dis 44:591-5

Showing the most recent 10 out of 12 publications