Green Tea Extract in Preventing Cancer in Former and Current Heavy Smokers With Abnormal Sputum

British Columbia Cancer Agency

Status and phase: Completed; Phase 2

Conditions: Tobacco Use Disorder; Lung Cancer

Treatments: Other: placebo; Drug: defined green tea catechin extract

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00573885

BCCA-R03-1083

BCCA-H03-61083

P01CA096964 (U.S. NIH Grant/Contract)

CDR0000578191

Details and patient eligibility

About

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming. Green tea extract may keep cancer from forming.

PURPOSE: This randomized phase II trial is studying green tea extract in preventing cancer in former and current heavy smokers with abnormal sputum.

Full description

OBJECTIVES:

• Evaluate the efficacy and safety of defined green tea catechin extract (polyphenon E) in former smokers with abnormal sputum score using stringent, newly developed response criteria of combined nuclear morphometry and malignancy-associated changes as the primary surrogate endpoint.
• Evaluate if polyphenon E can modulate other surrogate endpoint biomarkers of aberrant methylation, cell cycle regulation, apoptosis, oncogene/tumor suppressor gene expression, as well as phase I and II enzyme regulation.
• Establish a library of in-vivo confocal micro-endoscopy and optical coherent tomography images of the bronchial epithelium with corresponding histopathology, nuclear morphometry, and other biomarker information to assess the potential of confocal micro-endoscopy as a non-biopsy method to assess the effect of chemoprevention agents.

OUTLINE: This is an open label, part 1 study followed by a randomized, double-blind, part 2 study.

• Part 1 (completed March 22, 2006): Patients receive oral defined green tea catechin extract twice daily in months 1 and 2 and inhaled budesonide twice daily in month 2.

Patients undergo autofluorescence bronchoscopy with biopsies, oral and bronchial brushing, and bronchoalveolar lavage at the end of months 1 and 2.

• Part 2: Patients are stratified by gender and randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral defined green tea catechin extract twice daily for 6 months.
  • Arm II: Patients receive oral placebo twice daily for 6 months. Patients who have progressive or stable disease at 6 months may receive open-label defined green tea catechin extract.

Patients undergo autofluorescence bronchoscopy with biopsies, oral and bronchial brushing, and bronchoalveolar lavage at the end of months 6 and 12.

Blood samples are collected periodically for biomarker studies. After completion of study therapy, patients are followed periodically for 6 months.

Enrollment: 53 patients

Sex: All

Ages: 45 to 74 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Current smokers who have smoked at least 30 pack-years (e.g., 1 pack per day for 30 years or more) (part 1; completed March 22, 2006)

• Former smokers who have smoked at least 30 pack-years (part 2)

  • A former smoker is defined as one who has stopped smoking for one or more years

• Abnormal sputum score ≥ 0.25 by computer-assisted image analysis

• Exhaled carbon monoxide level < 5 ppm (part 2 )

• Willing to take defined green tea catechin extract/placebo twice a day regularly

• No evidence of overt lung cancer

  • No carcinoma in situ or invasive cancer on bronchoscopy or abnormal spiral chest CT suspicious of lung cancer

PATIENT CHARACTERISTICS:

Inclusion criteria:

• ECOG performance status 0-1
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• Creatinine normal
• Bilirubin normal
• AST and ALT normal
• Alkaline phosphatase normal

Exclusion criteria:

• Chronic active hepatitis/liver cirrhosis
• Severe heart disease (e.g., unstable angina, chronic congestive heart failure, use of antiarrhythmic agents)
• Ongoing gastric ulcer
• Acute bronchitis or pneumonia within one month
• Known reaction to lidocaine, albuterol sulfate, midazolam hydrochloride, and/or alfentanil hydrochloride
• Known allergy to green tea and/or corn starch, gelatin, or other nonmedicinal ingredients
• Any medical condition, such as acute or chronic respiratory failure or bleeding disorder that, in the opinion of the investigator, could jeopardize the patient's safety during participation in the study
• Unwilling to have a bronchoscopy
• Unwilling to have a spiral chest CT

PRIOR CONCURRENT THERAPY:

• No more than 5 cups of tea a week
• No concurrent anticoagulant treatment such as warfarin or heparin
• No use of other natural health products containing green tea compounds

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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53 participants in 2 patient groups, including a placebo group

Arm I

Experimental group

Description:

Patients receive oral defined green tea catechin extract twice daily for 6 months.

Treatment:

Drug: defined green tea catechin extract

Arm II

Placebo Comparator group

Description:

Patients receive oral placebo twice daily for 6 months.

Treatment:

Other: placebo