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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
British Columbia Cancer Agency
About
Eligibility
Locations
Arms
Outcomes
Full info

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

45 Years - 74 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    August 28, 2007
    Last Updated
    March 7, 2012
    Sponsor
    British Columbia Cancer Agency
    Collaborators
    National Cancer Institute (NCI)
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    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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