SGN-00101 Vaccine in Treating Human Papillomavirus in Patients Who Have Abnormal Cervical Cells

Cervical Cancer Clinical Trial

Official title:

An Exploratory Study to Evaluate the Effect of HPV 16 Vaccine on the Reduction of Viral Load in HPV 16 Positive Women With Persistent Viral Infection, But Low Grade Disease (ASCUS/LSIL)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00091130
• Other study ID #: NCI-2012-02623
• Secondary ID: UCI#02-55N01CN25
• Status: Completed
• Phase: Phase 2
• First received: September 7, 2004
• Last updated: May 31, 2013
• Start date: September 2004

Study information

• Verified date: March 2013
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This randomized phase II trial is studying how well SGN-00101 vaccine works compared to a placebo in treating human papillomavirus and preventing cervical cancer in patients with abnormal cervical cells. Vaccines, such as SGN-00101, may make the body build an immune response to kill human papillomavirus and abnormal cervical cells and may be effective in preventing cervical cancer

Description:

PRIMARY OBJECTIVES:

I. Compare the effectiveness of SGN-00101 vaccine vs placebo in reducing the human papillomavirus (HPV)-16 viral load in patients with atypical squamous cells of undetermined significance (ASCUS) or low-grade squamous intraepithelial lesions (LSIL) of the cervix with persistent HPV-16 infection who are at increased risk for developing a high-grade squamous intraepithelial lesion or invasive cervical cancer.

II. Compare the natural history of HPV-16 viral load in patients treated with these regimens.

III. Compare the effect of HPV-16 variants on viral load response in patients treated with these regimens.

IV. Compare the relative effectiveness of these regimens on the regression of cervical cellular atypias (based on Pap test results), in terms of the regression of cytologic findings of LSIL and ASCUS to normal findings and resolution or regression of colposcopically defined cervicovaginal lesions, in these patients.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive SGN-00101 vaccine subcutaneously (SC) on day 1 of weeks 1, 4, and 8 for a maximum of 3 injections in the absence of unacceptable toxicity or the development of an invasive malignancy or serious illness.

ARM II: Patients receive placebo vaccine SC on day 1 of weeks 1, 4, and 8 for a maximum of 3 injections in the absence of unacceptable toxicity or the development of an invasive malignancy or serious illness.

Patients are followed at 12, 24, and 52 weeks after the last vaccination.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 139
• Est. primary completion date: June 2007
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Meets criteria for 1 of the following groups:

• Prospective group, meeting the following criteria:

• Evidence of atypical squamous cells of undetermined significance (ASCUS) or low-grade squamous intraepithelial lesions (LSIL) by Pap test

• Human papillomavirus (HPV)-16-positive by polymerase chain reaction (PCR) and PGMY09/PGMY11 oligonucleotide primers viral load assay

• Medical records-based group, meeting the following criteria:

• Medical-record evidence of ASCUS or LSIL by Pap test within the past 6-12 months

• Meets 1 of the following criteria:

• Liquid-cytology findings of ASCUS or LSIL

• Colposcopic evidence of a LSIL by the Reid Index score of 1-5

• Historically persistent HPV-16-infection by PCR and HPV reverse transcription (RT)-PCR

• No evidence of high-grade squamous intraepithelial lesions (HSIL) by colposcopy (Reid Index = 6)

• Reports no sex partner change since last index Pap screening test

• Specimen-based group, meeting the following criteria:

• Medical-record evidence of ASCUS or LSIL by Pap test within the past 6-12 months

• Liquid-based cytology specimen available

• Meets 1 of the following criteria:

• Liquid-cytology findings of ASCUS or LSIL

• Colposcopic evidence of a LSIL by the Reid Index score of 1-5

• Historically persistent HPV-16-infection by PCR and, where measurable, HPV RT-PCR showing no greater than 3-fold reduction over the index liquid-cytology specimen

• No evidence of HSIL by colposcopy (Reid Index = 6)

• Menstrual period occurred at least once within the past 52 weeks

• No HSIL by Pap test within the past year

• Performance status - ECOG 0

• No severe or unstable coagulation

• Hepatitis B surface antigen negative

• Hepatitis C antibody negative

• No angina

• No heart failure

• No other cardiac condition

• No respiratory condition

• No asthma

• No immunological disorders (e.g., lupus, diabetes, multiple sclerosis, or myasthenia gravis)

• Not immunocompromised, suggestive of severe immune deficiency

• HIV negative

• No AIDS

• No active infection, defined as fever > 100° F

• No syphilis

• No severe allergic reactions (anaphylactic response) to drugs or any other allergen

• No history of allergy to any vaccine constituents, including cell- or tissue-system elements used to prepare the vaccine (e.g., bread products, yeast, or recombinant DNA technology using yeast systems)

• Must agree to use effective form of contraception throughout vaccination period

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during vaccination period and for 5 months after study treatment

• No sexual intercourse within 48 hours of virus specimen collection during study visits

• No objects (e.g., tampons, douche, suppositories, fingers, or toes) within the vagina or rectum within 48 hours of virus specimen collection during study visits

• No prior malignancy except nonmelanoma skin cancer

• No medical or psychiatric illness than would preclude study participation or compliance

• No other disorders requiring medical intervention that would preclude study participation

• No prior HPV vaccine

• More than 30 days since prior investigational vaccine

• More than 30 days since prior systemic steroid therapy

• No prior splenectomy

• More than 30 days since prior investigational drug

• More than 72 hours since prior antibiotic therapy for active infection

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Atypical Squamous Cells of Undetermined Significance
• Cervical Cancer
• High-grade Squamous Intraepithelial Lesion
• Low-grade Squamous Intraepithelial Lesion
• Uterine Cervical Neoplasms

Intervention

Biological:
• HspE7
Given SC

Other:
• placebo
Given SC
• laboratory biomarker analysis
Correlative studies

Locations

Country	Name	City	State
United States	University of California Medical Center At Irvine-Orange Campus	Orange	California

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	HPV-16 viral load	Following the univariate modeling, multivariate logistic regression models will be constructed by adding the demographic factors, baseline viral load, and type of cellular atypia to the model. The univariate logistic regression model for infection resolution is equivalent to a chi-square test.	6 months	No
Primary	Natural history of HPV 16 viral load	A repeated measures version of the zero-inflated log-normal model will be constructed.	Baseline	No
Primary	Natural history of HPV 16 viral load	A repeated measures version of the zero-inflated log-normal model will be constructed.	3 months	No
Primary	Natural history of HPV 16 viral load	A repeated measures version of the zero-inflated log-normal model will be constructed.	6 months	No
Primary	Regression or non-regression of the cellular atypia	The analysis for this will employ logistic regression models. A multivariate logistic regression model will be constructed. . A two group continuity corrected chi squared test with a 0.050 two-sided significance level will be used.	Up to 52 weeks	No
Secondary	HPV-16 viral load	Following the univariate modeling, multivariate logistic regression models will be constructed by adding the demographic factors, baseline viral load, and type of cellular atypia to the model. The univariate logistic regression model for infection resolution is equivalent to a chi-square test.	3 months	No
Secondary	Time to infection resolution	Kaplan Meier curves will be constructed.	Up to 52 weeks	No
Secondary	Time to disease resolution	Kaplan Meier curves will be constructed.	Up to 52 weeks	No