The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis

被引:1972
作者
Steinbach, G
Lynch, PM
Phillips, RKS
Wallace, MH
Hawk, E
Gordon, GB
Wakabayashi, N
Saunders, B
Shen, Y
Fujimura, T
Su, LK
Levin, B
Godio, L
Patterson, S
Rodriguez-Bigas, MA
Jester, SL
King, KL
Schumacher, M
Abbruzzese, J
DuBois, RN
Hittelman, WN
Zimmerman, S
Sherman, JW
Kelloff, G
机构
[1] Univ Texas, MD Anderson Canc Ctr, Div Canc Prevent, Houston, TX 77030 USA
[2] St Marks Hosp, Imperial Canc Res Fund, London EC1V 2PS, England
[3] NCI, Bethesda, MD 20892 USA
[4] GD Searle & Co, Skokie, IL 60077 USA
关键词
D O I
10.1056/NEJM200006293422603
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Patients with familial adenomatous polyposis have a nearly 100 percent risk of colorectal cancer. In this disease, the chemopreventive effects of nonsteroidal antiinflammatory drugs may be related to their inhibition of cyclooxygenase-2. Methods: We studied the effect of celecoxib, a selective cyclooxygenase-2 inhibitor, on colorectal polyps in patients with familial adenomatous polyposis. In a double-blind, placebo-controlled study, we randomly assigned 77 patients to treatment with celecoxib (100 or 400 mg twice daily) or placebo for six months. Patients underwent endoscopy at the beginning and end of the study. We determined the number and size of polyps from photographs and videotapes; the response to treatment was expressed as the mean percent change from base line. Results: At base line, the mean (+/-SD) number of polyps in focal areas where polyps were counted was 15.5+/-13.4 in the 15 patients assigned to placebo, 11.5+/-8.5 in the 32 patients assigned to 100 mg of celecoxib twice a day, and 12.3+/-8.2 in the 30 patients assigned to 400 mg of celecoxib twice a day (P=0.66 for the comparison among groups). After six months, the patients receiving 400 mg of celecoxib twice a day had a 28.0 percent reduction in the mean number of colorectal polyps (P = 0.003 for the comparison with placebo) and a 30.7 percent reduction in the polyp burden (the sum of polyp diameters) (P = 0.001), as compared with reductions of 4.5 and 4.9 percent, respectively, in the placebo group. The improvement in the extent of colorectal polyposis in the group receiving 400 mg twice a day was confirmed by a panel of endoscopists who reviewed the videotapes. The reductions in the group receiving 100 mg of celecoxib twice a day were 11.9 percent (P = 0.33 for the comparison with placebo) and 14.6 percent (P = 0.09), respectively. The incidence of adverse events was similar among the groups. Conclusions: In patients with familial adenomatous polyposis, six months of twice-daily treatment with 400 mg of celecoxib, a cyclooxygenase-2 inhibitor, leads to a significant reduction in the number of colorectal polyps. (N Engl J Med 2000;342:1946-52.) (C)2000, Massachusetts Medical Society.
引用
收藏
页码:1946 / 1952
页数:7
相关论文
共 40 条
  • [31] 2-J
  • [32] Cyclooxygenase-2 inhibitors in tumorigenesis (Part II)
    Taketo, MM
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (21): : 1609 - 1620
  • [33] ASPIRIN USE AND REDUCED RISK OF FATAL COLON CANCER
    THUN, MJ
    NAMBOODIRI, MM
    HEATH, CW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (23) : 1593 - 1596
  • [34] ALTERATIONS IN CELLULAR ADHESION AND APOPTOSIS IN EPITHELIAL-CELLS OVEREXPRESSING PROSTAGLANDIN-ENDOPEROXIDE-SYNTHASE-2
    TSUJII, M
    DUBOIS, RN
    [J]. CELL, 1995, 83 (03) : 493 - 501
  • [35] Regulation of cyclooxygenase-2 pathway by HER2 receptor
    Vadlamudi, R
    Mandal, M
    Adam, L
    Steinbach, G
    Mendelsohn, J
    Kumar, R
    [J]. ONCOGENE, 1999, 18 (02) : 305 - 314
  • [36] Vane JR, 1996, SCAND J RHEUMATOL, P9
  • [37] SULINDAC FOR POLYPOSIS OF THE COLON
    WADDELL, WR
    LOUGHRY, RW
    [J]. JOURNAL OF SURGICAL ONCOLOGY, 1983, 24 (01) : 83 - 87
  • [38] COMPLETE REVERSION AND PREVENTION OF RECTAL ADENOMAS IN COLECTOMIZED PATIENTS WITH FAMILIAL ADENOMATOUS POLYPOSIS BY RECTAL LOW-DOSE SULINDAC MAINTENANCE TREATMENT - ADVANTAGES OF A LOW-DOSE NONSTEROIDAL ANTIINFLAMMATORY DRUG REGIMEN IN REVERSING ADENOMAS EXCEEDING 33 MONTHS
    WINDE, G
    SCHMID, KW
    SCHLEGEL, W
    FISCHER, R
    OSSWALD, H
    BUNTE, H
    [J]. DISEASES OF THE COLON & RECTUM, 1995, 38 (08) : 813 - 830
  • [39] Gastrointestinal toxicity of nonsteroidal antiinflammatory drugs
    Wolfe, MM
    Lichtenstein, DR
    Singh, G
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (24) : 1888 - 1899
  • [40] Wolfe MM, 1999, NEW ENGL J MED, V341, P548