Celecoxib for the prevention of colorectal adenomatous polyps

被引:780
|
作者
Arber, Nadir
Eagle, Craig J.
Spicak, Julius
Racz, Istvan
Dite, Petr
Hajer, Jan
Zavoral, Miroslav
Lechuga, Maria J.
Gerletti, Paola
Tang, Jie
Rosenstein, Rebecca B.
Macdonald, Katie
Bhadra, Pritha
Fowler, Robert
Wittes, Janet
Zauber, Ann G.
Solomon, Scott D.
Levin, Bernard
机构
[1] Univ Texas, MD Anderson Canc Ctr, Div Canc Prevent & Populat Sci, Houston, TX 77030 USA
[2] Tel Aviv Sourasky Med Ctr, Integrated Canc Prevent Ctr, Tel Aviv, Israel
[3] Tel Aviv Univ, Sackler Sch Med, IL-69978 Tel Aviv, Israel
[4] Pfizer, New York, NY USA
[5] Inst Clin & Expt Med, Prague, Czech Republic
[6] Fac Hosp Brno Bohunice, Brno, Czech Republic
[7] Fac Hosp Kralovske Vinohrady, Prague, Czech Republic
[8] Cent Mil Hosp, Prague, Czech Republic
[9] Petz Aladar Cty Hosp, Gyor, Hungary
[10] Stat Collaborat, Washington, DC USA
[11] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[12] Brigham & Womens Hosp, Boston, MA 02115 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2006年 / 355卷 / 09期
关键词
D O I
10.1056/NEJMoa061652
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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收藏
页码:885 / 895
页数:11
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