Title: Eflornithine plus Sulindac for Prevention of Progression in Familial Adenomatous Polyposis
Author: Carol A. Burke, M.D.,, Evelien Dekker, M.D.,, Patrick Lynch, M.D.,, N. Jewel Samadder, M.D.,, Francesc Balaguer, M.D.,, Robert Hüneburg, M.D.,, John Burn, M.D.,, Antoni Castells, M.D.,, Steven Gallinger, M.D.,, Ramona Lim, M.D.,, Elena M. Stoffel, M.D.,, Samir Gupta, M.D.,, Alex Henderson, M.D.,, Frank G. Kallenberg, M.D.,, Priyanka Kanth, M.D.,, Victorine H. Roos, M.D.,, Gregory G. Ginsberg, M.D.,, Frank A. Sinicrope, M.D.,, Christian P. Strassburg, M.D.,, Eric Van Cutsem, M.D.,, James Church, M.D.,, Fiona Lalloo, M.D.,, Field F. Willingham, M.D., M.P.H.,, Paul E. Wise, M.D.,, William M. Grady, M.D.,, Molly Ford, M.D.,, Jennifer M. Weiss, M.D.,, Robert Gryfe, M.D.,, Anil K. Rustgi, M.D.,, Sapna Syngal, M.D.,, and Alfred Cohen, M.D.
The efficacy and safety of combination therapy with eflornithine and sulindac, as compared with either drug alone, in delaying disease progression in patients with familial adenomatous polyposis are unknown.
We evaluated the efficacy and safety of the combination of eflornithine and sulindac, as compared with either drug alone, in adults with familial adenomatous polyposis. The patients were stratified on the basis of anatomical site with the highest polyp burden and surgical status; the strata were precolectomy (shortest projected time to disease progression), rectal or ileal pouch polyposis after colectomy (longest projected time), and duodenal polyposis (intermediate projected time). The patients were then randomly assigned in a 1:1:1 ratio to receive 750 mg of eflornithine, 150 mg of sulindac, or both once daily for up to 48 months. The primary end point, assessed in a time-to-event analysis, was disease progression, defined as a composite of major surgery, endoscopic excision of advanced adenomas, diagnosis of high-grade dysplasia in the rectum or pouch, or progression of duodenal disease.
A total of 171 patients underwent randomization. Disease progression occurred in 18 of 56 patients (32%) in the eflornithine–sulindac group, 22 of 58 (38%) in the sulindac group, and 23 of 57 (40%) in the eflornithine group, with a hazard ratio of 0.71 (95% confidence interval [CI], 0.39 to 1.32) for eflornithine–sulindac as compared with sulindac (P=0.29) and 0.66 (95% CI, 0.36 to 1.24) for eflornithine–sulindac as compared with eflornithine. Among 37 precolectomy patients, the corresponding values in the treatment groups were 2 of 12 patients (17%), 6 of 13 (46%), and 5 of 12 (42%) (hazard ratios, 0.30 [95% CI, 0.07 to 1.32] and 0.20 [95% CI, 0.03 to 1.32]); among 34 patients with rectal or ileal pouch polyposis, the values were 4 of 11 patients (36%), 2 of 11 (18%), and 5 of 12 (42%) (hazard ratios, 2.03 [95% CI, 0.43 to 9.62] and 0.84 [95% CI, 0.24 to 2.90]); and among 100 patients with duodenal polyposis, the values were 12 of 33 patients (36%), 14 of 34 (41%), and 13 of 33 (39%) (hazard ratios, 0.73 [95% CI, 0.34 to 1.52] and 0.76 [95% CI, 0.35 to 1.64]). Adverse and serious adverse events were similar across the treatment groups.
In this trial involving patients with familial adenomatous polyposis, the incidence of disease progression was not significantly lower with the combination of eflornithine and sulindac than with either drug alone.