Nitric Oxide-Releasing Acetylsalicyclic Acid in Preventing Colorectal Cancer in Patients at High Risk of Colorectal Cancer

Last updated: February 6, 2009
Sponsor: Stony Brook University
Overall Status: Completed

Phase

1

Condition

Colorectal Cancer

Colon Cancer; Rectal Cancer

Rectal Cancer

Treatment

N/A

Clinical Study ID

NCT00331786
CDR0000473094
SUNY-UH-20055574
  • Ages > 50
  • All Genders

Study Summary

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of nitric oxide-releasing acetylsalicyclic acid may prevent colorectal cancer.

PURPOSE: This randomized phase I trial is studying the side effects and best dose of nitric oxide-releasing acetylsalicyclic acid in preventing colorectal cancer in patients at high risk of colorectal cancer.

Eligibility Criteria

Inclusion

DISEASE CHARACTERISTICS:

  • At risk for colorectal cancer

  • History of histologically proven sporadic colon adenomas or colon cancer

  • At least 5 aberrant cryptic foci on sigmoidoscopy

  • Less than 20 prior cumulative adenomas and no heredity nonpolyposis colorectal cancer

  • No significant asymptomatic lesions on sigmoidoscopy, including any of the following:

  • Inflammation

  • Strictures

  • Anorectal lesions

  • Fistulae

  • Vascular lesions

  • No adenomas or colon carcinomas on flexible sigmoidoscopy

  • No history of gastrointestinal (GI) cancer other than colorectal cancer

  • No inherited colorectal cancer syndromes

PATIENT CHARACTERISTICS:

  • No other GI mucosal epithelial diseases (e.g., Barrett's esophagus, chronic or recurrent peptic ulcer disease, celiac sprue, or other disorders of nutrient absorption)

  • No active peptic ulcer disease

  • No history of inflammatory bowel disease (ulcerative colitis or Crohn's disease)

  • No known or suspected alcohol ( > 5 glasses of wine or beer per day), drug, or medication abuse

  • No quantitative or qualitative platelet or coagulation abnormalities

  • No personal or family history of a bleeding disorder

  • No uncontrolled diabetes

  • No uncontrolled hypertension, or chronic congestive heart failure (New York Heart Association class II-IV heart disease)

  • No myocardial infarction, transient ischemic attack, or stroke within the past 6 months

  • No equilibrium disorders affecting gait or ability to stand that would preclude study participation

  • No involuntary change in weight (up or down) of ≥ 15% of usual body weight within the past year

  • Creatinine ≤ 2.0 mg/dL

  • No chronic liver disease or pancreatitis

  • No allergies to aspirin

  • No prior severe adverse reactions to NSAIDs such as asthma, GI bleeding, or renal insufficiency

  • No institutionalized, mentally disabled patients

  • No prisoners

  • Not pregnant or nursing

  • Fertile patients must use effective contraception

  • Negative pregnancy test

PRIOR CONCURRENT THERAPY:

  • No concurrent antibiotic prophylaxis

  • More than 7 days since prior nonsteroidal anti-inflammatory drug (NSAID) treatment, including aspirin

  • No concurrent frequent use (> 7 days in previous month) of NSAIDs, cyclooxygenase (COX)-2 inhibitors, nitrovasodilators, or oral corticosteroids

  • No concurrent macronutrient consumption below the 1st or above the 99th percentile of U.S. consumption

  • No concurrent anticoagulants, ticlopidine, and clopidogrel

  • More than 3 months since prior general anesthesia

  • More than 3 months since prior investigational agents

  • No concurrent NSAIDs, including aspirin or COX-2 inhibitors

  • Acetaminophen allowed

  • No concurrent nitrovasodilating drugs

  • More than 3 months since prior participation in other investigational trials

Study Design

Total Participants: 240
Study Start date:
July 01, 2006
Estimated Completion Date:

Study Description

OBJECTIVES:

Primary

  • Evaluate the effects of nitric oxide-releasing acetylsalicyclic acid on aberrant cryptic foci (ACF) in patients at high risk for colon cancer.

Secondary

  • Determine the pharmacokinetic profile of this drug in these patients.

  • Determine the presence or absence of ACF in these patients.

  • Determine the expression of PGE2, COX-1, COX-2, NF-kB, and β-catenin in colon tissue.

  • Determine the safety and tolerability of long-term nitric oxide-releasing acetylsalicyclic acid in these patients.

OUTLINE: This is a multicenter, double-blind, randomized, placebo-controlled, parallel group study. Patients are stratified according to gender and race (black vs non-Hispanic white vs Hispanic white vs Asian). Patients are randomized to 1 of 3 treatment arms.

  • Arm I: Patients receive oral nitric oxide-releasing acetylsalicyclic acid twice daily for 6 months.

  • Arm II: Patients receive nitric oxide-releasing acetylsalicyclic acid twice daily for 6 months at a higher dose than in arm I.

  • Arm III: Patients receive oral placebo twice daily for 6 months. Patients undergo sigmoidoscopies at baseline and at the completion of study treatment. Biopsies of aberrant cryptic foci (ACF) and non-ACF sites are collected at both sigmoidoscopies. Tissue is examined for biomarkers (PGE_2, COX, NF-kB, β-catenin).

After completion of study treatment, patients are followed periodically.

PROJECTED ACCRUAL: A total of 240 patients will be accrued for this study.

Connect with a study center

  • Stony Brook University Cancer Center

    Stony Brook, New York 11794-8174
    United States

    Site Not Available

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