Treatment of Colonic and Rectal Adenomas with Sulindac in Familial Adenomatous Polyposis
Francis M. Giardiello, Stanley R. Hamilton, Anne J. Krush, Steven Piantadosi, Linda M. Hylind, Paul Celano, Susan V. Booker, C. Rahj Robinson, and G. Johan A. Offerhaus
Background Familial adenomatous polyposis is an autosomal dominantdisorder characterized by the formation of hundreds of colorectaladenomas and eventual colorectal cancer. Administration of thenonsteroidal antiinflammatory drug sulindac has been followedby regression of polyps in patients with this disorder, butno controlled trial of this drug in patients who have not hadsurgery has been reported.
Methods We conducted a randomized, double-blind, placebo-controlledstudy of 22 patients with familial adenomatous polyposis, including18 who had not undergone colectomy. The patients received sulindacat a dose of 150 mg orally twice a day for nine months or identical-appearingplacebo tablets. The number and size of the polyps were evaluatedevery three months for one year.
Results A statistically significant decrease in the mean numberof polyps and their mean diameter occurred in patients treatedwith sulindac, as compared with those given placebo. When treatmentwas stopped at nine months, the number of polyps had decreasedto 44 percent of base-line values and the diameter of the polypsto 35 percent of base-line values (P = 0.014 and P<0.001,respectively, for the comparison with the changes in the groupgiven placebo). No patient had complete resolution of polyps.Three months after treatment with sulindac was stopped, boththe number and the size of the polyps increased in sulindac-treatedpatients but remained significantly lower than the values atbase line. No side effects from sulindac were noted.
Conclusions Sulindac reduces the number and size of colorectaladenomas in patients with familial adenomatous polyposis, butits effect is incomplete, and it is unlikely to replace colectomyas primary therapy.
Source Information
From the Departments of Medicine (F.M.G., A.J.K, L.M.H.) and Pathology (S.R.H., C.R.R.) and the Oncology Center (F.M.G., S.R.H., S.P., P.C., S.V.B.), Johns Hopkins University School of Medicine and Hospital, Baltimore; and the Department of Pathology, Academic Medical Center, Amsterdam, the Netherlands (G.J.A.O.).
Address reprint requests to Dr. Giardiello at the Gastroenterology Division, Blalock 935, Johns Hopkins Hospital, 600 N. Wolfe St., Baltimore, MD 21287.
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Higuchi, T., Iwama, T., Yoshinaga, K., Toyooka, M., Taketo, M. M., Sugihara, K.
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de Leng, W. W. J., Westerman, A. M., Weterman, M. A. J., de Rooij, F. W. M., Dekken, H. v., de Goeij, A. F. P. M., Gruber, S. B., Wilson, J. H. P., Offerhaus, G. J. A., Giardiello, F. M., Keller, J. J.
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Place, A. E., Suh, N., Williams, C. R., Risingsong, R., Honda, T., Honda, Y., Gribble, G. W., Leesnitzer, L. M., Stimmel, J. B., Willson, T. M., Rosen, E., Sporn, M. B.
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Sandler, R. S., Halabi, S., Baron, J. A., Budinger, S., Paskett, E., Keresztes, R., Petrelli, N., Pipas, J. M., Karp, D. D., Loprinzi, C. L., Steinbach, G., Schilsky, R.
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Baron, J. A., Cole, B. F., Sandler, R. S., Haile, R. W., Ahnen, D., Bresalier, R., McKeown-Eyssen, G., Summers, R. W., Rothstein, R., Burke, C. A., Snover, D. C., Church, T. R., Allen, J. I., Beach, M., Beck, G. J., Bond, J. H., Byers, T., Greenberg, E. R., Mandel, J. S., Marcon, N., Mott, L. A., Pearson, L., Saibil, F., van Stolk, R. U.
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