Zileuton in Preventing Lung Cancer in Patients With Bronchial Dysplasia

Lung Cancer Clinical Trial

Official title:

Phase II Trial Of Zileuton In Persons With Bronchial Dysplasia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00056004
• Other study ID #: CDR0000271915
• Secondary ID: P30CA022453WSU-D
• Status: Completed
• Phase: Phase 2
• First received: March 6, 2003
• Last updated: April 25, 2013
• Start date: June 2003
• Est. completion date: March 2009

Study information

• Verified date: April 2013
• Source: Barbara Ann Karmanos Cancer Institute
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. The use of zileuton may be an effective way to prevent lung cancer in patients who have bronchial dysplasia.

PURPOSE: Randomized phase II trial to study the effectiveness of zileuton in preventing lung cancer in patients who have bronchial dysplasia.

Description:

OBJECTIVES:

• Determine the efficacy of zileuton, in terms of number of sites and grade of dysplastic lesions in the bronchial epithelium, in patients with documented bronchial dysplasia.

• Correlate the regression of bronchial dysplasia (number and grade) and improvement in sputum cytology with the modulation of molecular biomarkers in patients treated with this drug.

• Determine the overall toxicity of this drug in these patients.

• Determine the 6-month natural history of bronchial dysplasia in patients who are randomized to receive treatment with a placebo.

OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are stratified according to smoking status (current vs recently quit smoker), and prior cancer (none vs lung or head and neck). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive oral zileuton 4 times daily for 6 months in the absence of disease progression or unacceptable toxicity.

• Arm II: Patients receive oral placebo 4 times daily for 6 months in the absence of disease progression or unacceptable toxicity.

Patients are followed at 4 weeks.

PROJECTED ACCRUAL: Approximately 134 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: March 2009
• Est. primary completion date: September 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• At high risk for dysplasia, defined by 1 of the following criteria:

• Current or former smokers who have smoked at least 30 pack-years

• Former smokers must be enrolled within 20 years of complete smoking cessation

• Patients with curatively treated stage I non-small cell lung cancer*

• Patients with curatively treated stage I or II squamous cell carcinoma of the head and neck (limited to oral cavity, pharynx, or larynx)* NOTE: *At least 12 months post-curative therapy

• Histologic confirmation of mild to severe bronchial dysplasia on bronchoscopic biopsy required

• Moderate or severe atypia on sputum cytology required before bronchoscopy (not required for patients with prior lung or head and neck cancer)

• No evidence of malignancy by chest x-ray

PATIENT CHARACTERISTICS:

Age

• 18 and over (for patients with prior lung or head and neck malignancy)

• 35 and over (for all other patients)

Performance status

• SWOG 0-1

Life expectancy

• Not specified

Hematopoietic

• WBC at least 3,000/mm^3

• Platelet count at least 100,000/mm^3

• Hemoglobin at least 10.0 g/dL

• No bleeding disorder

Hepatic

• Bilirubin no greater than upper limit of normal (ULN)

• Liver enzymes no greater than ULN

• PT/PTT no greater than ULN

• No active or chronic liver disease (even if transaminases have normalized)

Renal

• Creatinine no greater than ULN

Cardiovascular

• No unstable angina

• No uncontrolled heart failure

Pulmonary

• No significant asthma or chronic obstructive pulmonary disease requiring chronic or periodic (at least once per year) steroids for flares

• No acute or chronic respiratory failure

Other

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• Willing and able to undergo serial bronchoscopic examinations

• No ongoing alcohol use (i.e., at least 1 glass of wine, beer, or a mixed drink per day on a regular basis)

• No other medical condition that would preclude safety during study participation

• No other active or invasive malignancy within the past 5 years except basal cell skin cancer or carcinoma in situ of the cervix

• No hypersensitivity to study drug or any of its inactive ingredients

PRIOR CONCURRENT THERAPY:

Biologic therapy

• Not specified

Chemotherapy

• Not specified

Endocrine therapy

• More than 3 months since prior corticosteroids*

• No concurrent corticosteroids*

• No concurrent anticancer hormonal agents NOTE: *Systemic or inhaled, including chronic administration

Radiotherapy

• No concurrent radiotherapy

Surgery

• Not specified

Other

• More than 3 months since prior lipoxygenase inhibitors*

• More than 3 months since prior investigational agents

• More than 3 months since prior nutritional supplements (except 1 daily multivitamin)

• No concurrent nutritional supplements (except 1 daily multivitamin)

• No other concurrent lipoxygenase inhibitors*

• No other concurrent investigational agents

• No concurrent warfarin, beta-blockers, or theophylline

• No other concurrent antineoplastic agents

• No concurrent or chronic daily use of non-steroidal anti-inflammatory agents (NSAIDS) (except cardioprotective doses of aspirin less than 100 mg/day)

• Periodic use of NSAIDS allowed

• Concurrent participation in a smoking cessation program (including use of bupropion or nicotine gum or patch) allowed NOTE: *Systemic or inhaled, including chronic administration

Study Design

Allocation: Randomized, Masking: Double-Blind, Primary Purpose: Prevention

Related Conditions & MeSH terms

• Head and Neck Cancer
• Head and Neck Neoplasms
• Lung Cancer
• Lung Neoplasms

Intervention

Drug:
• zileuton

Locations

Country	Name	City	State
United States	Barbara Ann Karmanos Cancer Institute	Detroit	Michigan

Sponsors (2)

Lead Sponsor	Collaborator
Barbara Ann Karmanos Cancer Institute	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bronchial dysplasia number and grade at 6 months			No
Secondary	Biomarkers (Ki-67, Cyclin D1, bcl-2, bax, caspase-3) by immunohistochemistry at 6 and 12 months			No
Secondary	Biomarkers (5-HETE, LTB-4) by blood and BAL levels at 6 and 12 months			No
Secondary	Adverse events as measured by number and severity monthly			Yes