Authors |
Arber N, Eagle CJ, Spicak J, Racz I, Dite P, Hajer J, Zavoral M, Lechuga MJ, Gerletti P, Tang J, Rosenstein RB, Macdonald K, Bhadra P, Fowler R, Wittes J, Zauber AG, Solomon SD, Levin B; PreSAP Trial Investigators. |
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Title |
Celecoxib for the prevention of colorectal adenomatous polyps |
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Full source | N Engl J Med 2006;355:885-95 | |
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Abstract |
BACKGROUND:
Overexpression of cyclooxygenase 2 (COX-2) has been associated with colorectal
adenomatous polyps and cancer, prompting researchers to propose its inhibition
as a chemopreventive intervention. METHODS: The Prevention of Colorectal
Sporadic Adenomatous Polyps trial was a randomized, placebo-controlled,
double-blind study of the COX-2 inhibitor celecoxib given daily in a single
400-mg dose. At 107 centers in 32 countries, we randomly assigned 1561
subjects who had had adenomas removed before enrollment to receive celecoxib
(933 subjects) or placebo (628 subjects) daily, after stratification according
to the use or nonuse of low-dose aspirin. The primary outcome was detection
of adenomas at either year 1 or year 3 by colonoscopy and was compared
among the groups with the use of the Mantel-Cox test. RESULTS: Colonoscopies
were performed at year 1 on 88.7 percent of the subjects who had undergone
randomization and at year 3 on 79.2 percent. Of the 557 subjects in the
placebo group and the 840 subjects in the celecoxib group who were included
in the efficacy analysis, 264 and 270, respectively, were found to have
at least one adenoma at year 1, at year 3, or both. The cumulative rate
of adenomas detected through year 3 was 33.6 percent in the celecoxib
group and 49.3 percent in the placebo group (relative risk, 0.64; 95 percent
confidence interval, 0.56 to 0.75; P<0.001). The cumulative rate of
advanced adenomas detected through year 3 was 5.3 percent in the celecoxib
group and 10.4 percent in the placebo group (relative risk, 0.49; 95 percent
confidence interval, 0.33 to 0.73; P<0.001). Adjudicated serious cardiovascular
events occurred in 2.5 percent of subjects in the celecoxib group and
1.9 percent of those in the placebo group (relative risk, 1.30; 95 percent
confidence interval, 0.65 to 2.62). CONCLUSIONS: The use of 400 mg of
celecoxib once daily significantly reduced the occurrence of colorectal
adenomas within three years after polypectomy. (ClinicalTrials.gov number,
NCT00141193 [ClinicalTrials.gov].).
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