SGN-00101 in Preventing Anal Cancer in Patients With HIV Who Have Anal Neoplasia

NCT ID: NCT00052897

Last Updated: 2013-02-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-12-31

Brief Summary

Phase I/II trial to study the effectiveness of SGN-00101 in preventing anal cancer in HIV-positive patients who have high-grade anal neoplasia. Chemoprevention therapy is the use of certain drugs to try to prevent the development of cancer. SGN-00101 may be effective in preventing anal cancer.

Detailed Description

OBJECTIVES:

I. Determine the safety and maximum tolerated dose of SGN-00101 in HIV-positive patients with high-grade anal squamous intraepithelial lesions.

II. Determine clinical response and histologic/cytologic regression in patients treated with this drug.

III. Determine immune response in patients treated with this drug. IV. Determine the effect of this drug on HIV viral load and CD4 level in these patients.

OUTLINE: This is a dose-escalation study.

Patients receive SGN-00101 subcutaneously once on weeks 0, 4, and 8. Treatment continues in the absence of disease progression or unacceptable toxicity.

Cohorts of 5-6 patients receive escalating doses of SGN-00101 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose at which no more than 1 of 6 patients experience dose-limiting toxicity.

Patients are followed at 1, 4, and 10 months.

Conditions

Anal Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive SGN-00101 subcutaneously once on weeks 0, 4, and 8. Treatment continues in the absence of disease progression or unacceptable toxicity.

Cohorts of 5-6 patients receive escalating doses of SGN-00101 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose at which no more than 1 of 6 patients experience dose-limiting toxicity.

Group Type: EXPERIMENTAL

HspE7

Intervention Type: BIOLOGICAL

Interventions

HspE7

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed high-grade anal squamous intraepithelial lesions (HSIL) with residual HSIL of the anal canal or margin by high-resolution anoscopy

• Declined routine surgery or not a candidate for surgical excision of HSIL
• Documented evidence of HIV infection by one of the following methods:

• Serologic (ELISA or western blot)
• Culture
• Quantitative polymerase chain reaction or bDNA assays
• HIV RNA no greater than 500 copies/mL
• CD4 at least 200 x 10^6/L
• Must have received stable highly active antiviral therapy (HAART) for at least 4 weeks before study

• HAART defined as 3 or more agents, including a protease inhibitor or nonnucleoside reverse transcriptase inhibitor that is approved or available through expanded access combination antiviral therapy
• No prior history of invasive anal or cervical cancer
• No concurrent untreated cervical HSIL

PATIENT CHARACTERISTICS:

Age

• 18 and over

Life expectancy

• At least 12 months

Hematopoietic

• Hemoglobin at least 10 g/dL
• Platelet count at least 75,000/mm^3
• Absolute neutrophil count at least 1,000/mm^3

Hepatic

• AST and ALT no greater than 3 times upper limit of normal (ULN)

Renal

• Creatinine no greater than 1.5 times ULN

Immunologic

• No prior severe allergic reactions (i.e., anaphylactic response) to drugs or any other allergen
• No history of collagen-vascular or autoimmune disorder requiring treatment within the past 5 years
• No other concurrent illness that compromises the immune system
• No active serious opportunistic infection

Other

• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use 2 forms of effective contraception during and for 3 months after study
• No concurrent participation in a conception process (e.g., active attempt to become pregnant or impregnate, sperm donation, or in vitro fertilization)
• No other concurrent medical or psychiatric illness that would preclude study

PRIOR CONCURRENT THERAPY:

Biologic therapy

• No concurrent immunostimulants (including interferon or interleukin-12)

Chemotherapy

• More than 1 year since prior chemotherapy for cancer

Endocrine therapy

• No concurrent steroids that compromise immune function

• Concurrent topical corticosteroids allowed if dose determined not to suppress immune function

Radiotherapy

• More than 1 year since prior radiotherapy for cancer

Other

• More than 30 days since other prior investigational agents
• No concurrent medications that suppress immune function

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Joel Palefsky, MD

Role: STUDY_CHAIR

University of California, San Francisco

Locations

UCSF Comprehensive Cancer Center

San Francisco, California, United States

Countries

United States

Other Identifiers

AMC-035

Identifier Type: -

Identifier Source: secondary_id

CDR0000258786

Identifier Type: REGISTRY

Identifier Source: secondary_id

NCI-2012-02507

Identifier Type: -

Identifier Source: org_study_id