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A Study of the Effect of Polyphenon E (Green Tea Extract) on Breast Cancer Progression

Primary Purpose

Breast Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Polyphenon E
Sponsored by
Louisiana State University Health Sciences Center Shreveport
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Breast Cancer focused on measuring breast cancer, EGCG, Polyphenon E, c-Met, VEGF, HGF

Eligibility Criteria

21 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Definitive biopsy demonstrating primary breast cancer
  • Residual breast cancer requiring additional surgical resection
  • Stage I, II or III disease
  • Patient has ability to give signed informed consent
  • Normal hepatic and renal function (creatinine<1.5, transaminases <1.5 times upper limit of normal).
  • ECOG Performance status of 0 or 1.
  • Age ≥ 21 years and less than 75

Exclusion Criteria:

  • Prior hormonal or surgical therapy for breast cancer
  • Abnormal liver function test
  • Liver or kidney problems that would interfere with metabolism of study drug
  • Any condition that would hamper informed consent or ability to comply with study protocol
  • Participation in another research study in the last three months
  • Known malignancy at any site other than breast
  • Recent consumption of green tea (5 or more cups per day, within one week prior to biopsy)
  • Allergy or intolerance to any component of green tea
  • Inability or refusal to comply with definitive surgical therapy

Sites / Locations

  • LSU Health Sciences Center
  • Columbia Presbyterian Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Polyphenon E

Arm Description

This is a single arm study comparing changes within patients before and after receiving the experimental drug Polyphenon E for the duration of the study, between recruitment and surgery for breast cancer.

Outcomes

Primary Outcome Measures

Change in Serum VEGF in Breast Cancer
Change in serum VEGF from baseline to post treatment with polyphenon E.
Change in Serum HGF and Breast Cancer
Change in serum HGF from baseline to post Polyphenol E treatment.

Secondary Outcome Measures

Full Information

First Posted
May 9, 2008
Last Updated
August 23, 2017
Sponsor
Louisiana State University Health Sciences Center Shreveport
Collaborators
Columbia University
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1. Study Identification

Unique Protocol Identification Number
NCT00676793
Brief Title
A Study of the Effect of Polyphenon E (Green Tea Extract) on Breast Cancer Progression
Official Title
Phase II Clinical Trial to Determine if Polyphenon E Inhibits c-Met Signaling and Activation of Pathways Contributing to Breast Cancer Progression
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
May 2004 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Louisiana State University Health Sciences Center Shreveport
Collaborators
Columbia University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To see if an extract of green tea can affect certain markers of breast cancer and breast cancer progression in women with a recent biopsy positive for cancer and who are scheduled for surgery.
Detailed Description
To evaluate the short-term effects of a daily dose of Polyphenon E administered during the interval between breast biopsy and surgery in women with recently diagnosed breast cancer. Endpoints will be changes in serum and tissue biomarkers related to progression of cancer. The effect of Polyphenon E on tumor cell c-Met expression and phosphorylation is the primary objective. Secondary objectives include the effects on the other tissue and serum biomarkers. Evaluation of the safety and tolerability of Polyphenon E in this subject population is another objective. 1.1 Determine the effects of Polyphenon E on tumor cell c-Met expression and phosphorylation levels in patients with breast cancer 1.2 Determine the effects of Polyphenon E on PI-3K activation in patients with breast cancer 1.3 Determine the effects of Polyphenon E on MAPK activation in patients with breast cancer 1.4 Determine the effects of Polyphenon E on expression levels of other proteins involved in motility and invasion such as Rho GTPases and extracellular proteinases in patients with breast cancer 1.5 Determine the effects of Polyphenon E on markers of angiogenesis in patients with breast cancer 1.6 Determine the effects of Polyphenon E on other serum markers: C-reactive protein (CRP), Insulin-Like Growth factor I (IGF-I), Insulin-like Growth Factor Binding Protein 3 (IGFBP-3) and Hepatocyte Growth Factor HGF 1.7 Evaluate the safety and tolerability of Polyphenon E in this subject population

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
breast cancer, EGCG, Polyphenon E, c-Met, VEGF, HGF

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Polyphenon E
Arm Type
Experimental
Arm Description
This is a single arm study comparing changes within patients before and after receiving the experimental drug Polyphenon E for the duration of the study, between recruitment and surgery for breast cancer.
Intervention Type
Drug
Intervention Name(s)
Polyphenon E
Intervention Description
Four 200mg capsules daily taken with a meal, for the duration of the study.
Primary Outcome Measure Information:
Title
Change in Serum VEGF in Breast Cancer
Description
Change in serum VEGF from baseline to post treatment with polyphenon E.
Time Frame
Baseline and 4 to 6 weeks
Title
Change in Serum HGF and Breast Cancer
Description
Change in serum HGF from baseline to post Polyphenol E treatment.
Time Frame
Baseline and 4 to 6 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Definitive biopsy demonstrating primary breast cancer Residual breast cancer requiring additional surgical resection Stage I, II or III disease Patient has ability to give signed informed consent Normal hepatic and renal function (creatinine<1.5, transaminases <1.5 times upper limit of normal). ECOG Performance status of 0 or 1. Age ≥ 21 years and less than 75 Exclusion Criteria: Prior hormonal or surgical therapy for breast cancer Abnormal liver function test Liver or kidney problems that would interfere with metabolism of study drug Any condition that would hamper informed consent or ability to comply with study protocol Participation in another research study in the last three months Known malignancy at any site other than breast Recent consumption of green tea (5 or more cups per day, within one week prior to biopsy) Allergy or intolerance to any component of green tea Inability or refusal to comply with definitive surgical therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary Burton, M.D.
Organizational Affiliation
LSU Health Sciences Center Shreveport
Official's Role
Principal Investigator
Facility Information:
Facility Name
LSU Health Sciences Center
City
Shreveport
State/Province
Louisiana
ZIP/Postal Code
71103
Country
United States
Facility Name
Columbia Presbyterian Hospital
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Citations:
Citation
Proffered Oral Presentations - Intervention Studies Abstract PR-05: Effects of presurgical administration of tea polyphenols in women with operable breast cancer Julie L. Campbell1, James Cardelli2, Jerry McLarty2, Dawn Hershman1, Bret Taback1, Susan Refice1, Stephanie Wang2, Rebecca Bigelow2 and Katherine Crew1 1Columbia University Medical Center, New York, NY 2Louisiana State University Health Sciences Center, Shreveport, LA Cancer Prevention Research: December 2010; Volume 3, Issue 12, Supplement 2. doi: 10.1158/1940-6207.PREV-10-PR-05
Results Reference
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A Study of the Effect of Polyphenon E (Green Tea Extract) on Breast Cancer Progression

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