Folic Acid for the Prevention of Colorectal Adenomas: A Randomized Clinical Trial

• Published in: JAMA : the journal of the American Medical Association Vol. 297; no. 21; pp. 2351 - 2359
• Main Authors: Cole, Bernard F, Baron, John A, Sandler, Robert S, Haile, Robert W, Ahnen, Dennis J, Bresalier, Robert S, McKeown-Eyssen, Gail, Summers, Robert W, Rothstein, Richard I, Burke, Carol A, Snover, Dale C, Church, Timothy R, Allen, John I, Robertson, Douglas J, Beck, Gerald J, Bond, John H, Byers, Tim, Mandel, Jack S, Mott, Leila A, Pearson, Loretta H, Barry, Elizabeth L, Rees, Judy R, Marcon, Norman, Saibil, Fred, Ueland, Per Magne, Greenberg, E. Robert, Polyp Prevention Study Group, for the
• Format: Journal Article
• Language: English
• Published: United States American Medical Association 06-06-2007
• Subjects: Adenoma - epidemiology; Adenoma - etiology; Adenoma - prevention & control; Adult; Aged; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use; Aspirin - therapeutic use; Chi-Square Distribution; Clinical trials; Colon; Colorectal Neoplasms - epidemiology; Colorectal Neoplasms - prevention & control; Dietary supplements; Double-Blind Method; Female; Folic Acid - administration & dosage; Folic Acid - adverse effects; Folic Acid - therapeutic use; Follow-Up Studies; Humans; Incidence; Male; Middle Aged; Neoplasms - etiology; Preventive medicine; Risk; Treatment Failure; Tumors; Vitamin B
• DOI: 10.1001/jama.297.21.2351
• EISSN: 1538-3598
• ISSN: 0098-7484

CONTEXT Laboratory and epidemiological data suggest that folic acid may have an antineoplastic effect in the large intestine. OBJECTIVE To assess the safety and efficacy of folic acid supplementation for preventing colorectal adenomas. DESIGN, SETTING, AND PARTICIPANTS A double-blind, placebo-controlled, 2-factor, phase 3, randomized clinical trial conducted at 9 clinical centers between July 6, 1994, and October 1, 2004. Participants included 1021 men and women with a recent history of colorectal adenomas and no previous invasive large intestine carcinoma. INTERVENTION Participants were randomly assigned in a 1:1 ratio to receive 1 mg/d of folic acid (n = 516) or placebo (n = 505), and were separately randomized to receive aspirin (81 or 325 mg/d) or placebo. Follow-up consisted of 2 colonoscopic surveillance cycles (the first interval was at 3 years and the second at 3 or 5 years later). MAIN OUTCOME MEASURES The primary outcome measure was occurrence of at least 1 colorectal adenoma. Secondary outcomes were the occurrence of advanced lesions (≥25% villous features, high-grade dysplasia, size ≥1 cm, or invasive cancer) and adenoma multiplicity (0, 1-2, or ≥3 adenomas). RESULTS
During the first 3 years, 987 participants (96.7%) underwent colonoscopic follow-up, and the incidence of at least 1 colorectal adenoma was 44.1% for folic acid (n = 221) and 42.4% for placebo (n = 206) (unadjusted risk ratio [RR], 1.04; 95% confidence interval [CI], 0.90-1.20; P = .58). Incidence of at least 1 advanced lesion was 11.4% for folic acid (n = 57) and 8.6% for placebo (n = 42) (unadjusted RR, 1.32; 95% CI, 0.90-1.92; P = .15). A total of 607 participants (59.5%) underwent a second follow-up, and the incidence of at least 1 colorectal adenoma was 41.9% for folic acid (n = 127) and 37.2% for placebo (n = 113) (unadjusted RR, 1.13; 95% CI, 0.93-1.37; P = .23); and incidence of at least 1 advanced lesion was 11.6% for folic acid (n = 35) and 6.9% for placebo (n = 21) (unadjusted RR, 1.67; 95% CI, 1.00-2.80; P = .05). Folic acid was associated with higher risks of having 3 or more adenomas and of noncolorectal cancers. There was no significant effect modification by sex, age, smoking, alcohol use, body mass index, baseline plasma folate, or aspirin allocation.
CONCLUSIONS Folic acid at 1 mg/d does not reduce colorectal adenoma risk. Further research is needed to investigate the possibility that folic acid supplementation might increase the risk of colorectal neoplasia. TRIAL REGISTRATION
clinicaltrials.gov Identifier: NCT00272324