RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development of cancer. It is not yet known whether celecoxib is effective in preventing polyps in patients with colon cancer.

PURPOSE: Randomized phase III trial to study the effectiveness of celecoxib in preventing the development of polyps in patients who have undergone surgery for stage I colon cancer.

Condition	Treatment or Intervention	Phase
stage I colon cancer adenocarcinoma of the colon	Drug: celecoxib  Procedure: cancer prevention intervention  Procedure: chemoprevention of cancer	Phase III

Further Study Details: 

OBJECTIVES: Primary

• Compare celecoxib vs placebo, in terms of decreasing the incidence of adenomatous polyps of the colon and rectum, in patients with resected stage I adenocarcinoma of the colon.

Secondary

• Compare disease-free survival of patients treated with these regimens.
• Compare the effect of these regimens on self-reported symptoms and health-related quality of life of these patients.
• Compare the quality of life of patients treated with these regimens.
• Compare the benefits of celecoxib in patients with primary tumors or polyps that express cyclo-oxygenase-2 (COX-2) with those that do not express COX-2.
• Determine the toxicity and safety of celecoxib in these patients.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to gender, tumor stage (T1 vs T2), age (≤ 49 vs 50 to 59 vs ≥ 60 years), and current aspirin use (yes vs no). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive oral celecoxib twice daily for 3 years.
• Arm II: Patients receive oral placebo twice daily for 3 years. In both arms, treatment continues in the absence of unacceptable toxicity or the diagnosis of invasive colon cancer, carcinomaof the colon or rectum, or a non-colon primary cancer.

Quality of life is assessed at baseline and then at 6, 12, 24, 36, and 42 months.

Patients are followed at 6 months and at 2 years.

PROJECTED ACCRUAL: A total of 1,200 patients (600 per treatment arm) will be accrued for this study within 2.5 years.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed adenocarcinoma of the colon
• Stage I disease
• Distal border of tumor ≥ 12 cm from the anal verge
• Tumor completely resected within the past 90 days
• Must have undergone a preoperative or postoperative colonoscopy to the cecum (or small bowel anastomosis) within the past 90 days
• All observed polyps must have been removed
• Patients with a history suggestive of hereditary non-polyposis colorectal cancer (HNPCC) must have a normal microsatellite instability status by immunohistochemistry or polymerase chain reaction
• Patients with family history of colon cancer who have not been diagnosed with HNPCC are eligible
• No prior familial adenomatous polyposis
• No prior invasive cancer or carcinoma of the colon or rectum
• No clinical or radiologic evidence of metastatic disease

PATIENT CHARACTERISTICS: Age

• 18 and over

Performance status

• Zubrod 0-1

Life expectancy

• At least 10 years

Hematopoietic

• Complete blood count normal
• Platelet count normal

Hepatic

• AST normal
• Bilirubin normal
• Alkaline phosphatase normal

Renal

• Creatinine normal

Cardiovascular

• No active ischemic heart disease
• No New York Heart Association class III or IV heart disease
• No myocardial infarction within the past 6 months
• No symptomatic arrhythmia
• No symptomatic peripheral vascular disease or carotid disease that would preclude study participation

Pulmonary

• No aspirin-sensitive asthma

Gastrointestinal

• No history of inflammatory bowel disease
• No history of upper gastrointestinal bleeding
• No history of duodenal or gastric ulcer

Other

• No known hypersensitivity to any COX-2 inhibitor, NSAIDs, aspirin, or sulfonamides
• No non-colorectal malignancy within the past 5 years except carcinoma of the cervix, melanoma , or basal cell or squamous cell skin cancer
• No other disease that would preclude study participation
• No psychiatric disorders, including history of clinical depression or addictive disorders, that would preclude giving informed consent or long-term compliance
• No rheumatologic or skeletal disorders requiring chronic NSAIDs or steroid therapy
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY: Biologic therapy

• Not specified

Chemotherapy

• Not specified

Endocrine therapy

• Not specified

Radiotherapy

• Not specified

Surgery

• See Disease Characteristics

Other

• No other concurrent investigational agents for colon cancer
• No concurrent chronic use of other cyclo-oxygenase-2 (COX-2) inhibitors, non-steroidal anti-inflammatory drugs (NSAIDs), or salicylates (e.g., aspirin)
• Chronic use is defined as use for more than an average of 3 days per month
• Concurrent NSAIDs allowed for up to 10 consecutive days for temporary relief due to inflammatory syndromes, injury, or postoperative pain
• Cardioprotective doses of aspirin (≤ 81 mg/day or 325 mg every other day) allowed
• No concurrent fluconazole or lithium

Pennsylvania
      Allegheny General Hospital, Pittsburgh,  Pennsylvania,  15212-4772,  United States

Study chairs or principal investigators

Richard M. Goldberg, MD,  Principal Investigator,  UNC Lineberger Comprehensive Cancer Center   

Study ID Numbers:  CDR0000373869; NSABP-P-3; NCT00087256
Record last reviewed:  January 2005
Last Updated:  January 10, 2005
Record first received:  July 8, 2004
ClinicalTrials.gov Identifier:  NCT00087256
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08