Celecoxib for the prevention of sporadic colorectal adenomas

被引:866
作者
Bertagnolli, Monica M.
Eagle, Craig J.
Zauber, Ann G.
Redston, Mark
Solomon, Scott D.
Kim, KyungMann
Tang, Jie
Rosenstein, Rebecca B.
Wittes, Janet
Corle, Donald
Hess, Timothy M.
Woloj, G. Mabel
Boisserie, Frederic
Anderson, William F.
Viner, Jaye L.
Bagheri, Donya
Burn, John
Chung, Daniel C.
Dewar, Thomas
Foley, T. Raymond
Hoffman, Neville
Macrae, Finlay
Pruitt, Ronald E.
Saltzman, John R.
Salzberg, Bruce
Sylwestrowicz, Thomas
Gordon, Gary B.
Hawk, Ernest T.
机构
[1] Brigham & Womens Hosp, Div Surg Oncol, Boston, MA 02115 USA
[2] Pfizer, New York, NY USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[4] Univ Wisconsin, Madison, WI USA
[5] Stat Collaborat, Washington, DC USA
[6] NCI, Bethesda, MD 20892 USA
[7] CCS Associates, Mountain View, CA USA
[8] Newcastle Univ, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[9] Massachusetts Gen Hosp, Boston, MA 02114 USA
[10] Harris Methodist Hosp Ft Worth, Ft Worth, TX USA
[11] Reg Gastroenterol Associates Lancaster, Lancaster, PA USA
[12] Sir Charles Gairdner Hosp, Perth, WA, Australia
[13] Royal Melbourne Hosp, Melbourne, Vic, Australia
[14] Nashville Med Res Inst, Nashville, TN USA
[15] Atlanta Gastroenterol Associates, Atlanta, GA USA
[16] Univ Saskatchewan, St Pauls Hosp, Saskatoon, SK, Canada
[17] GD Searle & Co, Skokie, IL 60077 USA
关键词
D O I
10.1056/NEJMoa061355
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: Studies showing that drugs that inhibit cyclooxygenase-2 (COX-2) reduce the number of colorectal adenomas in animals and patients with familial adenomatous polyposis suggest that COX-2 inhibitors may also prevent sporadic colorectal neoplasia. Methods: We randomly assigned patients who had adenomas removed before study entry to receive placebo (679 patients) or 200 mg (685 patients) or 400 mg (671 patients) of celecoxib twice daily. Randomization was stratified for the use of low-dose aspirin. Follow-up colonoscopies were performed at one and three years after randomization. The occurrence of newly detected colorectal adenomas was compared among the groups with the life-table extension of the Mantel-Haenszel test. Results: Follow-up colonoscopies were completed at year 1 in 89.5 percent of randomized patients, and at year 3 in 75.7 percent. The estimated cumulative incidence of the detection of one or more adenomas by year 3 was 60.7 percent for patients receiving placebo, as compared with 43.2 percent for those receiving 200 mg of celecoxib twice a day (risk ratio, 0.67; 95 percent confidence interval, 0.59 to 0.77; P < 0.001) and 37.5 percent for those receiving 400 mg of celecoxib twice a day (risk ratio, 0.55; 95 percent confidence interval, 0.48 to 0.64; P < 0.001). Serious adverse events occurred in 18.8 percent of patients in the placebo group, as compared with 20.4 percent of those in the low-dose celecoxib group (risk ratio, 1.1; 95 percent confidence interval, 0.9 to 1.3; P=0.5) and 23.0 percent of those in the high-dose group (risk ratio, 1.2; 95 percent confidence interval, 1.0 to 1.5; P=0.06). As compared with placebo, celecoxib was associated with an increased risk of cardiovascular events (risk ratio for the low dose, 2.6; 95 percent confidence interval, 1.1 to 6.1; and risk ratio for the high dose, 3.4; 95 percent confidence interval, 1.5 to 7.9). Conclusions: These findings indicate that celecoxib is an effective agent for the prevention of colorectal adenomas but, because of potential cardiovascular events, cannot be routinely recommended for this indication.
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页码:873 / 884
页数:12
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