Eflornithine and Sulindac in Preventing Colorectal Cancer in Patients With Colon Polyps

National Cancer Institute (NCI)

Status and phase: Completed; Phase 3

Conditions: Precancerous Condition

Treatments: Drug: eflornithine; Other: placebo; Other: laboratory biomarker analysis; Drug: sulindac

Study type: Interventional

Funder types: NIH

Identifiers

NCT00118365

R01CA088078 (U.S. NIH Grant/Contract)

NCI-2009-00880

UCI 97-05

Details and patient eligibility

About

This randomized phase III trial is studying eflornithine and sulindac to see how well they work compared to a placebo in preventing colorectal cancer in patients with colon polyps. Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. The use of eflornithine and sulindac may prevent colorectal cancer. It is not yet known whether eflornithine and sulindac are more effective than a placebo in preventing colorectal cancer

Full description

PRIMARY OBJECTIVES:

I. Compare the rate of new adenomatous polyp formation in patients with a history of adenomatous polyps of the colon treated with eflornithine and sulindac vs placebo.

II. Correlate the effects of eflornithine and sulindac on polyamine and prostaglandin content in the flat mucosa with the rate of new adenoma formation in these patients.

III. Compare the rate of side effects in patients treated with these regimens.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to participating center and aspirin use (yes vs no).

Patients receive oral double placebo once daily for 4 weeks. Patients who are more than 70% compliant by pill measurement or self reporting are randomized to 1 of 2 treatment arms.

Arm I: Patients receive oral double placebo once daily.

Arm II: Patients receive oral eflornithine (DFMO) and oral sulindac once daily.

In both arms, treatment continues for 36 months in the absence of unacceptable toxicity or the development of an invasive malignancy.

Enrollment: 375 patients

Sex: All

Ages: 40 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Criteria:

• History of >= 1 surgically resected adenomatous polyp of the colon measuring >= 3 mm within the past 5 years
• Screening colonoscopy performed within the past 6 months
• All polyps must have been removed during colonoscopy, pathologically examined, and archived
• No prior surgical resection removing > 40 cm of the colon
• No personal or family history of familial polyposis or hereditary non-polyposis colon cancer
• SWOG 0-1
• Bilirubin =< 2.0 mg/dL
• AST and ALT =< 2 times normal
• Creatinine =< 1.5 mg/dL
• Urine protein =<, urine casts 0-3, urine WBC and RBC count 0-5 cells by urinalysis
• No history of inflammatory bowel disease
• No gastric or duodenal ulcers within the past 12 months
• Gastric or duodenal ulcers that were adequately treated > 24 months ago are allowed
• No symptomatic gastric or duodenal ulcers
• Not pregnant or nursing
• Negative pregnancy test
• Must have regional geographic stability over the next 36 months
• Pure tone audiometry evaluation normal
• Patients with >= 20 dB of uncorrectable hearing loss (for age) of any 2 contiguous frequencies are not allowed
• No invasive malignancy within the past 5 years except adequately treated nonmelanoma skin cancer, level I (or Breslow < 0.76 mm) cutaneous melanoma, Duke's A colon cancer, stage I cervical cancer, or stage 0 chronic lymphocytic leukemia
• No severe metabolic disorder
• No other significant acute or chronic disease that would preclude study participation
• No history of abnormal wound healing or repair
• No conditions that would confer risk of abnormal wound healing or repair
• No history of allergy to NSAIDs or eflornithine
• No concurrent chemotherapy
• No concurrent corticosteroids on a regular or predictable intermittent basis
• No concurrent radiotherapy
• Concurrent calcium supplements (=< 1,000 mg/day) allowed
• Concurrent lipid-lowering drugs (i.e., high-dose statins) allowed
• No other concurrent nonsteroidal anti-inflammatory drugs (NSAIDs) on a regular or predictable intermittent basis
• Concurrent aspirin for cardiovascular prophylaxis (i.e., 81 mg/day) allowed
• No concurrent anticoagulants on a regular or predictable intermittent basis
• No concurrent treatment for gastric or duodenal ulcers

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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375 participants in 2 patient groups, including a placebo group

Arm II (placebo)

Placebo Comparator group

Description:

Patients receive oral double placebo once daily. In both arms, treatment continues for 36 months in the absence of unacceptable toxicity or the development of an invasive malignancy.

Treatment:

Other: laboratory biomarker analysis

Other: placebo

Arm I (eflornithine and sulindac)

Experimental group

Description:

Patients receive oral eflornithine (DFMO) and oral sulindac once daily. In both arms, treatment continues for 36 months in the absence of unacceptable toxicity or the development of an invasive malignancy.

Treatment:

Drug: sulindac

Other: laboratory biomarker analysis

Drug: eflornithine