Aspirin and Zileuton and Biomarker Expression in Nasal Tissue of Current Smokers

NCT ID: NCT02348203

Last Updated: 2022-06-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 63 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-01-13
• Study Completion Date: 2021-03-09

Brief Summary

This randomized phase II trial studies the effects of aspirin and zileuton on genes related to tobacco use in current smokers. Aspirin and zileuton may interfere with genes related to tobacco use and may be useful in preventing lung cancer in current smokers.

Detailed Description

PRIMARY OBJECTIVES:

I. To analyze the impact of combined treatment of acetylsalicylic acid (ASA) (aspirin) and zileuton on smoking-related gene expression signature in the nasal epithelium in current smokers and to analyze any difference between the ASA and zileuton intervention and placebo control.

SECONDARY OBJECTIVES:

I. To assess the impact of ASA and zileuton on three lung cancer gene signatures (an 80-gene bronchial signature, a phosphatidylinositol 3-kinase [PI3K] pathway gene signature and a nasal diagnostic gene signature) and to compare this to placebo control.

II. To determine whether the change in the smoking-related gene expression signature and the three lung cancer gene signatures of nasal epithelium persists 10-14 days off agent intervention.

III. To measure urinary prostaglandin E metabolite (PGE-M) and leukotriene E(4) (LTE[4]) levels in current smokers after ASA and zileuton.

IV. To assess the safety in current smokers of 12 week exposure to ASA and zileuton.

V. To evaluate a gender effect in the modulatory effects of ASA and zileuton on smoking related-gene expression signature.

VI. To explore the effect of ASA and zileuton on the metabolomics profile of the arachidonic acid pathway.

VII. To explore, in a discovery-driven fashion, the effect of ASA and zileuton on whole-genome gene expression.

VIII. To analyze the impact of ASA and zileuton on karyometric analysis of buccal cells.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM I: Patients receive aspirin orally (PO) once daily (QD) and zileuton PO twice daily (BID) for 12 weeks in the absence of unacceptable toxicity.

ARM II: Patients receive aspirin placebo PO QD and zileuton placebo PO BID for 12 weeks.

After completion of study treatment, patients are followed up for 2 weeks.

Conditions

Tobacco Use Disorder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Study Groups

Arm I (aspirin, zileuton)

Patients receive aspirin PO QD and zileuton PO BID for 12 weeks in the absence of unacceptable toxicity.

Group Type: EXPERIMENTAL

Aspirin

Intervention Type: DRUG

Given PO

Laboratory Biomarker Analysis

Intervention Type: OTHER

Correlative studies

Zileuton

Intervention Type: DRUG

Given PO

Arm II (double placebo)

Patients receive aspirin placebo PO QD and zileuton placebo PO BID for 12 weeks.

Group Type: PLACEBO_COMPARATOR

Laboratory Biomarker Analysis

Intervention Type: OTHER

Correlative studies

Placebo Administration

Intervention Type: OTHER

Given aspirin placebo PO

Placebo Administration

Intervention Type: OTHER

Given zileuton placebo PO

Interventions

Aspirin

Given PO

Intervention Type: DRUG

Laboratory Biomarker Analysis

Correlative studies

Intervention Type: OTHER

Placebo Administration

Given aspirin placebo PO

Intervention Type: OTHER

Placebo Administration

Given zileuton placebo PO

Intervention Type: OTHER

Zileuton

Given PO

Intervention Type: DRUG

Other Intervention Names

Acetylsalicylic Acid; ASA; Aspergum; Ecotrin; Empirin; Entericin; Extren; Measurin; Zyflo

Eligibility Criteria

Inclusion Criteria

• Current tobacco smokers with >= 20 pack years of self-reported smoking exposure and an average use of >= 10 cigarettes/day
• Karnofsky >= 70%
• Leukocytes >= 3,000/microliter
• Absolute neutrophil count >= 1,500/microliter
• Hematocrit >= the lower institutional limit
• Platelets >= the lower institutional limits
• Total bilirubin within normal institutional limits
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) within normal institutional limits
• Creatinine =< the upper institutional limits
• Prothrombin time (PT)/partial thromboplastin time (PTT) within normal institutional limits
• Fertile subjects must use adequate contraception (abstinence, barrier methods, or birth control pills) prior to study entry and for the duration of study participation; women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her study physician immediately
• Participants may have a history of indeterminate pulmonary nodule(s) by chest imaging if nodule follow-up has been completed or the study procedures would not interfere with nodule follow-up
• Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria

• History of allergic reaction to aspirin or attributed to compounds of similar chemical or biologic composition to aspirin, including other nonsteroidal anti-inflammatory drugs (NSAIDs)
• Gastric intolerance attributable to ASA or NSAIDs
• History of gastric ulcer within the past 5 years (with or without bleeding)
• Use of ASA or NSAIDs for more than 5 days per month within 3 months of enrollment
• Not willing or are unable to refrain from use of any non-study ASA, NSAIDs and leukotriene antagonists during the study period
• Adult asthma
• Chronic, current or recent (within the past three months) use of leukotriene antagonists
• Require chronic anticoagulation or anti-platelet therapy
• History of bleeding disorder or hemorrhagic stroke
• Chronic, current or recent (within the past three months) use of glucocorticoids (systemic, topical and/or nasal sprays or steroid topical creams to large body surface area); use of steroid topical creams for small body areas (=< 10% body surface) during study intervention is allowed
• History of chronic sinusitis or recent nasal polyps
• History of, or current, active or chronic liver disease even if transaminases have normalized
• History of allergic reaction to zileuton or attributed to compounds of similar chemical or biologic composition to zileuton
• Are taking drugs known to interact with zileuton, including theophylline, warfarin, and propranolol
• Not willing or are unable to limit alcohol consumption to =< 2 alcoholic beverages a day during the study period
• Pregnant or lactating women; breastfeeding should be discontinued if the mother is treated with aspirin; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her study physician immediately
• Participants may not be receiving any other investigational agents
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• Have a known history of inability to absorb an oral agent
• Invasive cancer within the past five years except non-melanoma skin cancer
• Urine cotinine level, if collected at screening, does not confirm active smoking status

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Linda L Garland

Role: PRINCIPAL_INVESTIGATOR

The University of Arizona Medical Center-University Campus

Locations

Banner University Medical Center - Tucson

Tucson, Arizona, United States

Boston University School of Medicine

Boston, Massachusetts, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

NCI-2015-00061

Identifier Type: REGISTRY

Identifier Source: secondary_id

N01-CN-2012-00031

Identifier Type: -

Identifier Source: secondary_id

1403269898

Identifier Type: OTHER

Identifier Source: secondary_id

UAZ2013-02-01

Identifier Type: OTHER

Identifier Source: secondary_id

N01CN00031

Identifier Type: NIH

Identifier Source: secondary_id

View Link

P30CA023074

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2015-00061

Identifier Type: -

Identifier Source: org_study_id