Green Tea Extract in Preventing Cervical Cancer in Patients With Human Papillomavirus and Low-Grade Cervical Intraepithelial Neoplasia

• Status: Completed
• Trial end date: 2011-02-01
• Target enrollment: 0
• Participant gender: Female

Summary

This randomized phase II trial is studying green tea extract to see how well it works compared to a placebo in preventing cervical cancer in patients with human papillomavirus and low-grade cervical intraepithelial neoplasia. Chemoprevention is the use of certain substances to keep cancer from forming, growing, or coming back. The use of green tea extract may stop cervical cancer from forming in patients with human papillomavirus and low-grade cervical intraepithelial neoplasia. It is not yet known whether green tea extract is more effective than a placebo in preventing cervical cancer in patients with human papillomavirus and low-grade cervical intraepithelial neoplasia.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Cancer Institute (NCI)
• Treatments: Epigallocatechin gallate

Criteria

Inclusion Criteria:

• Histologically confirmed cervical intraepithelial neoplasia 1 (CIN 1) AND oncogenic human papillomavirus (HPV) positivity

• At increased risk for developing cervical cancer due to >= 1 of the following criteria (documented 6-12 months ago)*:

• Positive oncogenic HPV on DNA hybrid capture

• Low-grade squamous intraepithelial lesion cytology

• Histopathologically documented CIN 1 on cervical biopsy [Note: *Patients must now have current CIN 1 by histology or colposcopy AND HPV positivity]

• Cervical dysplasia by colposcopy OR positive biopsy

• No invasive cervical cancer or high-grade intraepithelial neoplasia on cervical biopsy or endocervical curettage

• ECOG performance status < 2

• Total bilirubin < 2 times upper limit of normal (ULN)

• AST < 2 times ULN

• ALT normal

• Creatinine < 2.0 mg/dL

• Able and willing to return to clinic for study visits once every 4 weeks for the duration of the study

• No history of allergic reaction to tea or related dietary products

• No HIV positive patients (or AIDS/HIV-associated complex)

• No uncontrolled intercurrent illness including, but not limited to, any of the following:

• Ongoing or active infection other than HPV

• Symptomatic congestive heart failure

• Unstable angina pectoris

• Cardiac arrhythmia

• Psychiatric illness/social situation that would limit compliance with study requirements

• No history of any cancer except nonmelanoma skin cancer

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No regular intake of 6 or more servings of tea per week within 1 month prior to study entry

• No treatment for genital condyloma within 30 days prior to study entry

• No prior pelvic irradiation

• No concurrent tea (green, black, or oolong) or tea-derived products

• No other concurrent investigational agents