Modeling Study to Predict Progression of Anal Cancer Pre-cursor Lesions in HIV

This study is currently recruiting participants. (see Contacts and Locations)
Verified October 2012 by National Institute of Allergy and Infectious Diseases (NIAID)
Sponsor:
Collaborators:
University of Cincinnati
Cincinnati VA Medical Center
Information provided by (Responsible Party):
Jaime Robertson, University of Cincinnati
ClinicalTrials.gov Identifier:
NCT01709448
First received: October 16, 2012
Last updated: NA
Last verified: October 2012
History: No changes posted

October 16, 2012
October 16, 2012
January 2009
March 2014   (final data collection date for primary outcome measure)
histological diagnosis of high-grade squamous intra-epithelial lesion confirmed by anal biopsy [ Time Frame: 12 months, 24 months, 36 months ] [ Designated as safety issue: No ]
Same as current
No Changes Posted
Regression of lesions defined by normal appearance on anoscopy and normal histology on anal biopsy following previous diagnosis of squamous intraepithelial lesion. [ Time Frame: 12 months, 24 months, 36 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Modeling Study to Predict Progression of Anal Cancer Pre-cursor Lesions in HIV
Predictive Modeling of Anal Dysplasia Progression in HIV

The purpose of this study is to determine whether a model can be created to predict the progression of early anal cancer precursor lesions in HIV using potential predictors such as: HIV treatment history, smoking history, sexual history, human papillomavirus viral load, human papillomavirus protein expression, and cell markers associated with progression of HPV-related lesions.

Persons living with HIV-infection are at greatly increased risk for anal carcinoma and anal intraepithelial neoplasia (AIN). Despite the overall improvement in HIV outcomes, the incidence of anal carcinoma has not decreased with the advent of highly active antiretroviral ther-apy. Further, there is substantial morbidity and mortality associated with anal carcinoma in HIV-infected individuals. For these reasons, it is critically important to develop effective screening and treatment strategies in this population. Anal carcinoma is similar to cervical carcinoma in that they are both associated with infection with human papillomavirus (HPV) and share similar cytologic features of dysplasia. Anal cytology screening is ultimately expected to reduce the incidence of anal carcinoma similar to that seen with cervical cancer after the introduction of cervical Pap screening. Given the high frequency of abnormal cytology in patients with HIV and the need to confirm results by high-resolution anoscopy, however, the implementation of screening programs requires a substantial commitment of clinical resources. The workload and costs involved in following up on abnormal cytology reduce the cost-effectiveness of screening and pose a significant barrier to its widespread integration into routine HIV care. A model for predicting which patients are at greatest risk for progressive of anal dysplasia is needed in order to decrease the need for excessive confirmatory procedures in this population. Without such a model, anal carcinoma screening may remain cost prohibitive for many HIV clinics.

The objective of this study is to develop a predictive model to identify patients who are at greatest risk for progression of anal intraepithelial neoplastic changes. The central hypotheses are: 1) that progression of early HPV-related anal dysplasia is associated with environmental, virological, and host molecular factors and 2) that it is possible to develop a predictive statistical model with a high sensitivity and specificity for predicting disease progression. These hypotheses have been formulated on the basis of strong evidence from studies of HPV-related cervical dysplasia that smoking, HPV E2 expression, HPV E6/E7 protein expression, high-risk HPV type, HPV viral load, p16 expression, p53 expression and Ki67 expression are associated with progressive cervical dysplasia. The rationale for the proposed research is that development of a predictive model will allow clinicians to design more cost-effective screening and follow-up strategies which focus resources on intensively testing only those patients with a significant risk for progression. Further, the models developed will allow clinicians to identify a population of patients who may benefit from early treatment interventions. Finally, information learned from this research may provide information applicable to other HPV-related cancers.

Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
Description:

Anal cytology Anal biopsies

Non-Probability Sample

HIV primary care clinic

  • Neoplasms, Squamous Cell
  • Papillomavirus Infections
Not Provided
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
165
March 2014
March 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • HIV-infected
  • Age > 18 years old
  • Abnormal anal screening cytology

Exclusion Criteria:

  • Inability to sign informed consent
  • Life-threatening illness or other contraindication for high-resolution anoscopy
  • anal intraepithelial neoplasia not confirmed by anal biopsy
  • history of anal carcinoma
  • history of HPV vaccination
Both
18 Years and older
No
Contact: Jaime C Robertson, MD (513) 584-5827 roberj5@ucmail.uc.edu
Contact: Eva Moore, RN (513) 584-4819 mooreev@ucmail.uc.edu
United States
 
NCT01709448
1K23AI080202-01, 1K23AI080202-01
No
Jaime Robertson, University of Cincinnati
National Institute of Allergy and Infectious Diseases (NIAID)
  • University of Cincinnati
  • Cincinnati VA Medical Center
Principal Investigator: Jaime C Robertson, MD University of Cincinnati
National Institute of Allergy and Infectious Diseases (NIAID)
October 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP