Colon Cancer Clinical Trial
Selenium for Prevention of Adenomatous Colorectal Polyps
Summary
RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Selenium may be effective in preventing the recurrence of adenomatous colorectal polyps.
PURPOSE: This randomized phase III trial is studying selenium to see how well it works in preventing the recurrence of polyps in patients with adenomatous colorectal polyps.
Full Description
OBJECTIVES:
Primary
Compare the effects of selenium vs placebo on the recurrence of adenomatous colorectal polyps, in terms of histologic type, degree of dysplasia, number, size, and location, in patients with adenomatous colorectal polyps.
Compare the type, incidence, and outcome of side effects in patients treated with these regimens.
Determine patient adherence to long-term treatment with these regimens.
Secondary
Determine the effects of regimen modification by baseline blood selenium level, low-dose aspirin, selenoprotein genetic marker polymorphisms (e.g., GPx-1, GPx-2, and SEP15)
Determine the effects of low-dose aspirin (81 mg/day) modification by ornithine decarboxylase promoter genotype, and toxicity by slow-metabolizer genotypes of the cytochrome p450 2C9 and UT1A6 loci in these patients.
OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to use of low-dose (≤ 81 mg/day) aspirin (yes vs no). Patients are randomized to 1 of 2 treatment arms.
Arm I: Patients receive oral selenium once daily.
Arm II: Patients receive oral placebo once daily. In both arms, treatment continues for up to 5 years* in the absence of disease progression or unacceptable toxicity.
Patients undergo follow-up colonoscopy approximately 5 years* after baseline colonoscopy.
NOTE: Some patients will continue participation for up to 7 and a half years
PROJECTED ACCRUAL: A total of 1,600 patients with an adenoma will be randomized to this study, followed by a second group of randomization of 200 patients with at least one advanced adenoma (at baseline) for a substudy. Total planned randomizations = 1,800 participants.
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically confirmed colorectal adenomatous polyps
Meets the following criteria by colonoscopy (performed within the past 6 months):
Cecum was totally visualized or reached
At least 90% visualization of colon surface area
Removed at least 1 adenomatous polyp of at least 3 mm in size during procedure (For the Advanced Adenoma Sub-study: Removal of at least 1 advanced colorectal adenomatous polyp during procedure. An adenoma is considered advanced if it is 10 mm or greater in size, and/or has villous histology and/or shows high grade dysplasia)
Removed no more than 10 adenomatous polyps of any size by endoscopy
All other neoplastic and non-neoplastic colon polyps must have been completely removed (except for diminutive [less than 3 mm] sessile rectal polyps)
For the sub-study, at least 1 advanced adenomatous polyp defined as 10 mm or greater in size and/or has villous histology and/or shows high grade dysplasia
No prior diagnosis of any of the following:
Colorectal cancer
Familial adenomatous polyposis
Ulcerative colitis
Crohn's disease
Hereditary non-polyposis colon cancer (HNPCC), defined as:
Histologically confirmed colorectal cancer in at least 3 relatives, 1 of whom is a first-degree relative of the other 2
Disease occurrence in at least 2 consecutive generations
Colorectal cancer diagnosis in at least 1 family member who is less than 50 years of age
Patients with a family history of colorectal cancer but who are not diagnosed with HNPCC are allowed
No more than 1 prior segmental colon resection
PATIENT CHARACTERISTICS:
Age
40 to 80
Performance status
SWOG 0-1
Life expectancy
Not specified
Hematopoietic
Hemoglobin > 11 g/dL
WBC 3,000 - 11,000/mm^3
Hepatic
AST and ALT < 2 times upper limit of normal
Bilirubin < 2.0 mg/dL
Renal
Creatinine < 1.9 mg/dL
Cardiovascular
No unstable* cardiac disease despite medication (e.g., diuretics or digitalis)
No uncontrolled hypertension (i.e., systolic blood pressure ≥ 170 mm Hg and/or diastolic blood pressure ≥ 110 mm Hg) despite medication NOTE: *Unstable defined as unable to walk across the room without chest pain or shortness of breath
Other
Not pregnant or nursing
Fertile patients must use effective contraception for at least 2 months before and during study treatment
Resident of a clinical center metropolitan area or obtaining regular health care in a clinical metropolitan area for at least 6 months out of the year
Must be able to swallow pills
No unexpected weight loss of 10% or more within the past 6 months
No prior rheumatoid arthritis
No poorly controlled diabetes mellitus despite medication, defined as:
Blood sugar level ≥ 200 mg/dL on more than half of the readings taken within the past month
No invasive malignancy within the past 5 years that required medical excision, radiotherapy, or chemotherapy except basal cell or squamous cell carcinoma
PRIOR CONCURRENT THERAPY:
Biologic therapy
No concurrent drugs that regulate the immune system
Chemotherapy
No concurrent chemotherapy
Endocrine therapy
Not specified
Radiotherapy
No concurrent radiotherapy
Surgery
See Disease Characteristics
Other
Prior enrollment in another adenoma prevention study allowed
Concurrent routine aspirin (≤ 81 mg/day) allowed
No regular use of non-steroidal anti-inflammatory drugs (NSAIDs)
No concurrent enrollment in another research study using pharmacological cancer drugs, a cyclo-oxygenase-2 inhibitor, or selenium
No other concurrent selenium unless dosage is ≤ 50 µg/day
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There are 7 Locations for this study
Phoenix Arizona, 85012, United States
Scottsdale Arizona, 85258, United States
Scottsdale Arizona, 85259, United States
Tucson Arizona, 85724, United States
Denver Colorado, 80220, United States
Williamsville New York, 14221, United States
Dallas Texas, 75246, United States
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