Infrared Coagulator Ablation or Observation in Preventing Anal Cancer in HIV-Positive Patients With Anal Neoplasia

You may be eligible if

• DISEASE CHARACTERISTICS:
• Diagnosis of high-grade anal intraepithelial neoplasia (AIN) meeting the following:
• * AIN2 and/or AIN3 confirmed by biopsy ≥ 2 weeks to ≤ 60 days before enrollment
• * 1-3 lesions with each lesion ≤ 15 mm in diameter
• * At least one high-grade AIN lesion is still visible at study entry
• HIV-infection documented by federally approved, licensed HIV-test in conjunction with screening test (e.g., ELISA, western blot, or other test)
• * HIV-infection, based on prior ELISA and western blot assays, recorded and documented by another physician, allowed provided patient undergoes an approved antibody test to confirm diagnosis
• * Patients on concurrent anti-retroviral therapy with a history of HIV-positivity based on an approved antibody test allowed
• * Detectable plasma HIV-1 RNA also allowed
• No perianal AIN, perianal condyloma, or lower vulvar intraepithelial neoplasia or condyloma requiring treatment
• PATIENT CHARACTERISTICS:
• Karnofsky performance status 70-100%
• Life expectancy ≥ 2 years
• CD4 count ≥ 200/mm³
• ANC \> 750/mm³
• Platelet count ≥ 75,000/mm³
• Hemoglobin ≥ 9.0 g/dL
• INR and aPTT normal
• Negative pregnancy test
• Fertile patients must use effective contraception
• Female patients must have undergone cervical pap smear (if having a cervix) and gynecologic evaluation within the past 12 months
• Must be capable of complying with the requirements of this protocol
• Concurrent HPV-related disease allowed
• No history of anal cancer
• No acute infection or other serious medical illness requiring treatment within the past 14 days
• * Fungal infection of the skin or a sexually transmitted disease requiring treatment allowed
• No concurrent malignancy requiring systemic therapy
• * Kaposi sarcoma limited to the skin allowed
• PRIOR CONCURRENT THERAPY:
• No prior infrared coagulator (IRC) ablation for high-grade anal intraepithelial neoplasia (HGAIN)
• * Prior HGAIN treated by any means other than IRC within the past 2 months allowed
• At least 5 days since prior coumadin or clopidogrel and ≥ 7 days after study therapy before receiving coumadin or clopidogrel again
• No concurrent anticoagulant therapy other than aspirin or NSAIDs
• More than 3 months since prior and concurrent systemic corticosteroids, cytokines, or immunomodulatory therapy (e.g., interferons) or local imiquimod
• No concurrent systemic therapy