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Summary

at San Francisco, California and other locations
study started
estimated completion:

Description

Summary

This phase II trial studies surgery in treating patients with anal canal or perianal cancer that is small and has not spread deeply into the tissues and human immunodeficiency virus (HIV) infection. Local surgery may be a safer treatment with fewer side effects than bigger surgery or radiation and chemotherapy.

Official Title

A Multicenter Observational and Feasibility Study of Excision of Superficially Invasive Squamous Cell Carcinoma (SISCCA) of the Anal Canal and Perianus in HIV-Infected Persons

Details

PRIMARY OBJECTIVES:

  1. To define the proportion of participants who develop treatment failure at 2 years, defined as the occurrence of distant or any nodal metastases or recurrence of cancer requiring chemotherapy (CMT), defined as a cancer that no longer meets the definition of superficially invasive squamous cell carcinoma (SISCCA) or a cancer that cannot be excised with a clear margin or preservation of sphincter function, or those who develop SISCCA recurrence but elect to undergo CMT rather than repeat excision in patients originally treated with excision of anal canal and perianal SISCCA.

II. To define the 1-year proportion of participants who develop incident anal squamous cancers at sites other than the location of the index SISCCA in patients treated with excision of anal canal and perianal SISCCA.

SECONDARY OBJECTIVES:

  1. To define the proportion of participants who develop treatment failure at 3 years, defined as occurrence of distant or any nodal metastases or recurrence of cancer requiring CMT, defined as a cancer that no longer meets the definition of SISCCA or a cancer that cannot be excised with a clear margin or preservation of sphincter function or those who develop SISCCA recurrence but elect to undergo CMT rather than repeat excision in patients treated with excision of anal canal and perianal SISCCA.

II. To determine morbidities associated with local excision of SISCCA, including non-healing ulcer, fissure, persistent pain and bleeding, stricture, incontinence, and colostomy 6 months after excision of SISCCA.

EXPLORATORY OBJECTIVES:

  1. To determine the human papillomavirus (HPV) type in cancer and compare to that of overlying high-grade squamous intraepithelial lesions (HSIL) and HSIL biopsies collected concurrently that did not progress to cancer.

II. To determine and compare the HPV integration site in the anal cancer as well as in HSIL overlying or contiguous with the cancer and HSIL biopsies collected concurrently that did not progress to cancer.

III. Perform gene expression array analysis comparing expression in anal cancer with HSIL overlying or contiguous with the cancer.

IV. Perform gene expression array analysis comparing expression in HSIL biopsies that progressed to cancer with non-progressing HSIL biopsies at other locations.

  1. Characterize genetic changes in anal cancers compared with HSIL overlying or contiguous with the cancer.

VI. Characterize genetic changes in HSIL biopsies that progressed to cancer compared with non-progressing HSIL biopsies at other locations.

VII. Perform gene expression array analysis and characterize genetic changes of SISCCAs that were cured with wide local excision for comparison with SISCCAs that progressed after wide local excision.

OUTLINE:

Patients undergo surgery to remove anal or perianal cancer. Any HSIL remaining is treated with the goal for complete eradication in accordance with clinician and participant preference.

After completion of study treatment, patients are followed up every 3 months for 36 months.

Keywords

Anal Squamous Cell Carcinoma HIV Infection Stage 0 Anal Canal Cancer Stage I Anal Canal Cancer Carcinoma Infection Carcinoma, Squamous Cell HIV Infections Acquired Immunodeficiency Syndrome Anus Neoplasms

Eligibility

You can join if…

  • A single, biopsy-proven SISCCA as defined by the LAST criteria (=< 3mm depth of invasion, horizontal spread of =< 7 mm, and completely excised with at least 1 mm margin clear of cancer irrespective of the amount of HSIL) documented within 8 weeks of enrollment
  • No evidence of any lymph node spread or distant metastases as determined by positron emission tomography (PET) computed tomography (CT) imaging within 8 weeks of enrollment; alternatively for those without PET CT capability, a magnetic resonance imaging (MRI) or CT of the abdomen and pelvis and a chest x-ray confirming no evidence of metastatic disease is acceptable
  • Clinician believes that eradication of concomitant HSIL is reasonable and feasible based on the extent of disease and overall medical condition of the subject
  • HIV-1 infection, as documented by any federally approved, licensed HIV test performed in conjunction with screening (or enzyme-linked immunosorbent assay [ELISA], test kit,and confirmed by Western blot or other approved test); alternatively, this documentation may include a record demonstrating that another physician has documented the participant's HIV status based on either: 1) approved diagnostic tests or 2)relevant medical history and/or current management of HIV infection
  • Prior to Segment A enrollment, patients on combination anti-retroviral therapy (cART)will be required to have a minimum cluster of differentiation (CD)4 count of >= 200 and patients not on cART will be required to have a minimum CD4 count of >=350 to be eligible for the study; patients not currently on cART who have a CD4 count > 200 and who agree to start cART immediately will be eligible for participation; laboratory data should be obtained within 12 weeks prior to enrollment
  • Participants must have Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  • Participants must have a life expectancy of 2 years or more
  • Participants must not have any other concurrent malignancy
  • Leukocytes: >= 3,000/mm3

  • Absolute neutrophil count: >= 1,500/mm3

  • Platelets: >= 100,000/mm3

  • Women of childbearing potential must have a negative urine pregnancy test within 72 hours prior to enrollment; female participants are advised to not become pregnant during study participation; all women of childbearing potential must agree to use a reliable birth control method (oral contraceptive pills, intrauterine device,Nexplanon, DepoProvera, or permanent sterilization, etc., or another acceptable method as determined by the investigator) during the entire period of the trial (3 years),and must not intend to become pregnant during study participation and for 3 months after treatment is discontinued
  • Men should not father a child while in this study; men who could father a child must agree to use at least one form of birth control during the study and for 3 months after stopping all study treatment
  • Participants must be able to understand and willing to sign a written informed consent document
  • Participants must, in the opinion of the Investigator, be capable of complying with the requirements of this protocol

You CAN'T join if...

  • Anal cancer that cannot be completely excised with a >=1 mm clear margin from surrounding tissue or where excision to obtain a clear margin would compromise sphincter function or anal canal diameter
  • Concurrent anal canal or perianal HSIL or condyloma that in the judgment of the clinician cannot be cleared or can only be cleared with undue morbidity to the patient
  • Prior pelvic radiation therapy that would preclude radiation therapy if anal cancer develops
  • Ongoing use of anticoagulant therapy other than aspirin or non-steroidal anti-inflammatory drugs (NSAIDS) that cannot be stopped for surgical procedures
  • Acute treatment for an infection (excluding fungal infection of the skin and sexually transmitted infections) or other serious medical illness within 2 weeks before enrollment
  • Current systemic chemotherapy or radiation therapy that potentially causes bone marrow suppression that would preclude safe treatment of HSIL; Note: Kaposi's sarcoma limited to the skin is not exclusionary unless requiring systemic chemotherapy
  • Prior HPV vaccination
  • Patients who are receiving any other investigational agents within 4 weeks prior to enrollment; investigational antiretroviral agents for HIV are acceptable
  • Participant plans to relocate away from the study site during study participation

Locations

  • University of California, San Francisco accepting new patients
    San Francisco, California, 94115, United States
  • Laser Surgery Care accepting new patients
    New York, New York, 10011, United States
  • Boston Medical Center accepting new patients
    Boston, Massachusetts, 02118, United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
AIDS Malignancy Consortium
ID
NCT02437851
Phase
Phase 2
Lead Scientist
J Berry
Study Type
Interventional
Last Updated
July 20, 2017
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