ACAPHA in Preventing Lung Cancer in Former Smokers With Bronchial Intraepithelial Neoplasia
Primary Purpose
Lung Cancer, Precancerous Condition
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
multi-herbal agent ACAPHA
Sugar Pill
Sponsored by
About this trial
This is an interventional prevention trial for Lung Cancer focused on measuring non-small cell lung cancer, small cell lung cancer, squamous lung dysplasia
Eligibility Criteria
DISEASE CHARACTERISTICS:
- One or more areas of bronchial intraepithelial neoplasia (IEN) (metaplasia/dysplasia) with a nuclear morphometry index > 1.36 and a surface diameter > 1.2 mm on autofluorescence bronchoscopy
- Atypical sputum cells as determined by computer-assisted image analysis
- Former smoker (i.e., stopped smoking at least 1 year ago) who has smoked at least 30 pack-years (i.e., 1 pack/day for 30 years or more)
- Exhaled carbon monoxide level < 5 ppm
- No invasive cancer on bronchoscopy or abnormal spiral chest CT scan suspicious of lung cancer
PATIENT CHARACTERISTICS:
- ECOG performance status 0 or 1
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- Normal renal function tests (BUN, creatinine, urinalysis)
- Normal liver function tests (AST, ALT, bilirubin, alkaline phosphatase)
- No chronic active hepatitis or liver cirrhosis
- No acute bronchitis or pneumonia within the past month
- No known reaction to xylocaine
No medical condition that, in the opinion of the investigator, could jeopardize the patient's safety during participation in the study, including any of the following:
- Acute or chronic respiratory failure
- Unstable angina
- Uncontrolled congestive heart failure
- Bleeding disorder
PRIOR CONCURRENT THERAPY:
- Not specified
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
ACAPHA
Sugar Pill
Arm Description
Outcomes
Primary Outcome Measures
Efficacy and safety of multi-herbal agent ACAPHA as measured by combined histopathology and nuclear morphometry of intraepithelial neoplasia lesions
Secondary Outcome Measures
Changes in the severity of dysplasia by bronchial biopsy
Changes in the morphometric index of sputum cells, bronchial biopsies, and epithelial cells in the bronchoalveolar lavage fluid (BAL)
MIB-1, bcl-2, and TUNEL immunostaining in the bronchial biopsies
Methylation biomarkers in the sputa, oral brush, and BAL cells
Gene expression analysis of RNA from bronchial brush cells
Volumetric measurement of CT scan-detected lung nodules before and after treatment
Full Information
NCT ID
NCT00522197
First Posted
August 28, 2007
Last Updated
March 7, 2012
Sponsor
British Columbia Cancer Agency
Collaborators
National Cancer Institute (NCI)
1. Study Identification
Unique Protocol Identification Number
NCT00522197
Brief Title
ACAPHA in Preventing Lung Cancer in Former Smokers With Bronchial Intraepithelial Neoplasia
Official Title
A Phase II Trial of ACAPHA in Former Smokers With Intraepithelial Neoplasia
Study Type
Interventional
2. Study Status
Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
November 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
British Columbia Cancer Agency
Collaborators
National Cancer Institute (NCI)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming. The use of ACAPHA, a combination of six herbs, may prevent lung cancer from forming in former smokers with bronchial intraepithelial neoplasia.
PURPOSE: This randomized phase II trial is studying the side effects and how well ACAPHA works in preventing lung cancer in former smokers with bronchial intraepithelial neoplasia.
Detailed Description
OBJECTIVES:
Determine the efficacy and safety of multi-herbal agent ACAPHA in former smokers with bronchial intraepithelial neoplasia.
Evaluate whether ACAPHA can modulate other surrogate endpoint biomarkers of aberrant methylation, cell cycle regulation, apoptosis, as well as phase I and II enzyme regulation.
Establish a library of in vivo confocal microendoscopy images with corresponding histopathology, nuclear morphometry, and other biomarker information to assess the potential of confocal microendoscopy as a nonbiopsy method in assessing the effect of chemoprevention agents.
OUTLINE: Patients are stratified according to gender. Patients are randomized to 1 of 2 arms.
Arm I: Patients receive oral multi-herbal agent ACAPHA twice daily for 6 months. Patients achieving a partial response receive an additional 6 months of ACAPHA.
Arm II: Patients receive oral placebo twice daily for 6 months. Patients achieving a partial response receive an additional 6 months of placebo. Patients with progressive disease receive ACAPHA twice daily for 6 months.
Patients undergo sputum cytology, oral and bronchial brushings, bronchoalveolar lavage, and bronchial tissue biopsies at baseline and at 6 and 12 months. Samples are analyzed for histopathological and morphometric cell changes; MIB-1 bcl-2, and TUNEL immunostaining; methylation biomarkers; and gene expression analysis of RNA.
After completion of study therapy, patients are followed at 1 and 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Precancerous Condition
Keywords
non-small cell lung cancer, small cell lung cancer, squamous lung dysplasia
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ACAPHA
Arm Type
Active Comparator
Arm Title
Sugar Pill
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
multi-herbal agent ACAPHA
Intervention Type
Dietary Supplement
Intervention Name(s)
Sugar Pill
Primary Outcome Measure Information:
Title
Efficacy and safety of multi-herbal agent ACAPHA as measured by combined histopathology and nuclear morphometry of intraepithelial neoplasia lesions
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Changes in the severity of dysplasia by bronchial biopsy
Time Frame
6 months
Title
Changes in the morphometric index of sputum cells, bronchial biopsies, and epithelial cells in the bronchoalveolar lavage fluid (BAL)
Time Frame
12 months
Title
MIB-1, bcl-2, and TUNEL immunostaining in the bronchial biopsies
Time Frame
12 months
Title
Methylation biomarkers in the sputa, oral brush, and BAL cells
Time Frame
12 months
Title
Gene expression analysis of RNA from bronchial brush cells
Time Frame
12 months
Title
Volumetric measurement of CT scan-detected lung nodules before and after treatment
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS:
One or more areas of bronchial intraepithelial neoplasia (IEN) (metaplasia/dysplasia) with a nuclear morphometry index > 1.36 and a surface diameter > 1.2 mm on autofluorescence bronchoscopy
Atypical sputum cells as determined by computer-assisted image analysis
Former smoker (i.e., stopped smoking at least 1 year ago) who has smoked at least 30 pack-years (i.e., 1 pack/day for 30 years or more)
Exhaled carbon monoxide level < 5 ppm
No invasive cancer on bronchoscopy or abnormal spiral chest CT scan suspicious of lung cancer
PATIENT CHARACTERISTICS:
ECOG performance status 0 or 1
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception
Normal renal function tests (BUN, creatinine, urinalysis)
Normal liver function tests (AST, ALT, bilirubin, alkaline phosphatase)
No chronic active hepatitis or liver cirrhosis
No acute bronchitis or pneumonia within the past month
No known reaction to xylocaine
No medical condition that, in the opinion of the investigator, could jeopardize the patient's safety during participation in the study, including any of the following:
Acute or chronic respiratory failure
Unstable angina
Uncontrolled congestive heart failure
Bleeding disorder
PRIOR CONCURRENT THERAPY:
Not specified
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen Lam, MD
Organizational Affiliation
British Columbia Cancer Agency
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
ACAPHA in Preventing Lung Cancer in Former Smokers With Bronchial Intraepithelial Neoplasia
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