Lack of Effect of a High-Fiber Cereal Supplement on the Recurrence of Colorectal Adenomas
David S. Alberts, M.D., María Elena Martínez, Ph.D., Denise J. Roe, Dr.P.H., José M. Guillén-Rodríguez, M.S., James R. Marshall, Ph.D., J. Barbara van Leeuwen, M.A., Mary E. Reid, Ph.D., Cheryl Ritenbaugh, Ph.D., Perla A. Vargas, Ph.D., A.B. Bhattacharyya, M.D., David L. Earnest, M.D., Richard E. Sampliner, M.D., Dianne Parish, Kris Koonce, Lianne Fales, for The Phoenix Colon Cancer Prevention Physicians' Network
Background The risks of colorectal cancer and adenoma, the precursorlesion, are believed to be influenced by dietary factors. Epidemiologicevidence that cereal fiber protects against colorectal canceris equivocal. We conducted a randomized trial to determine whetherdietary supplementation with wheat-bran fiber reduces the rateof recurrence of colorectal adenomas.
Methods We randomly assigned 1429 men and women who were 40to 80 years of age and who had had one or more histologicallyconfirmed colorectal adenomas removed within three months beforerecruitment to a supervised program of dietary supplementationwith either high amounts (13.5 g per day) or low amounts (2g per day) of wheat-bran fiber. The primary end point was thepresence or absence of new adenomas at the time of follow-upcolonoscopy. Subjects and physicians, including colonoscopists,were unaware of the group assignments.
Results Of the 1303 subjects who completed the study, 719 hadbeen randomly assigned to the high-fiber group and 584 to thelow-fiber group. The median times from randomization to thelast follow-up colonoscopy were 34 months in the high-fibergroup and 36 months in the low-fiber group. By the time of thelast follow-up colonoscopy, at least one adenoma had been identifiedin 338 subjects in the high-fiber group (47.0 percent) and in299 subjects in the low-fiber group (51.2 percent). The multivariateadjusted odds ratio for recurrent adenoma in the high-fibergroup, as compared with the low-fiber group, was 0.88 (95 percentconfidence interval, 0.70 to 1.11; P=0.28), and the relativerisk of recurrence according to the number of adenomas, in thehigh-fiber group as compared with the low-fiber group, was 0.99(95 percent confidence interval, 0.71 to 1.36; P=0.93).
Conclusions As used in this study, a dietary supplement of wheat-branfiber does not protect against recurrent colorectal adenomas.
The risks of colorectal cancer and adenoma, the precursor lesion,are believed to be influenced by diet.1 Burkitt's proposal thata high-fiber diet protects against colon cancer was based onthe low rates of colorectal cancer in Africa.2 Insoluble fibers,such as wheat-bran fiber, are thought to protect against coloncancer by absorbing carcinogens in the gastrointestinal tract.3Indeed, wheat-bran fiber has been shown to dilute fecal concentrationsof bile acids4,5 and to bind bile acids, thereby increasingtheir fecal excretion.6,7 Although an inverse correlation wasobserved between mortality rates from colon cancer and per capitacereal consumption,8 the results of the few analytical epidemiologicstudies of associations between the consumption of whole-graincereal and the risk of colorectal cancer9,10,11,12,13,14,15or adenoma16 have been equivocal. Some metabolic end-point studies,5,17including our own,4 have shown that wheat-bran fiber decreasesfecal mutagenicity and reduces concentrations of fecal bileacids, although no effect was found on rates of proliferationof rectal mucosal cells.18 Two studies found that a supplementof wheat-bran fiber had no effect on the risk of recurrent colorectaladenoma.19,20
In 1990, we initiated a multicenter trial to determine whetherwheat-bran fiber can prevent the recurrence of colorectal adenomas.
Methods
Study Design and Subjects
Details of the design and methods of the study have been describedpreviously.21 Briefly, subjects were recruited between September1990 and July 1995 from multiple centers in the Phoenix, Arizona,metropolitan area. The study protocol was approved by the institutionalreview boards of the 22 participating health care centers inthe Phoenix area and by the human-subjects committee of theUniversity of Arizona. All subjects provided written informedconsent.
We identified men and women who were 40 to 80 years of age fromwhom one or more colorectal adenomas, measuring at least 3 mmin diameter at colonoscopy, had been removed within the threemonths before recruitment. To be eligible, subjects had to havean adequate nutritional status and normal renal and liver functionand to have a Southwest Oncology Group performance status of0, 1, or 2.22 We excluded persons who had had invasive cancerwithin the previous five years; those with a history of colonresection; those who had two or more first-degree relativeswith colorectal cancer, severe metabolic disorders, or othersevere illnesses; and those with an intake of more than 30 gof dietary fiber per day on the basis of their responses tothe Arizona Food-Frequency Questionnaire.23
Subjects who successfully completed a six-week run-in periodby consuming at least 75 percent of the amount of a low-fibersupplement supplied (2 g per day) were randomly assigned toreceive a high-fiber supplement (13.5 g per day) or a low-fibersupplement (2 g per day) of wheat-bran cereal. With the exceptionof the cereal-fiber intervention, no other dietary changes wererequired. The treatment assignments were not revealed to thesubjects, their physicians, or members of the study staff. Thefiber supplements were provided by Kellogg (Battle Creek, Mich.)and were available in several forms: unsweetened loop-shapedcereal and sweetened and unsweetened shredded cereal. Analysisof the fiber content per serving showed the following: high-fiberloops, 13 g; low-fiber loops, 2 g; high-fiber unsweetened shreddedcereal, 13 g; low-fiber unsweetened shredded cereal, 4 g; high-fibersweetened shredded cereal, 10 g; and low-fiber sweetened shreddedcereal, 3 g. Cereal boxes were color coded into six groups tohelp maintain the study blinding. Midway through the study,high-fiber wheat-branfiber bars (containing 10 g of fiber)and low-fiber bars (4 g of fiber) were developed by Kellogg.Subjects who had completed two years of the study were allowedto elect to consume up to 25 percent of their daily fiber supplementin the form of a fiber bar.
Compliance with the protocol was evaluated primarily by countsof returned cereal boxes and fiber bars at each visit and secondarilythrough a specialized intake calendar. Each index was used togenerate an overall compliance score; subjects who consumedmore than 75 percent of the cereal supplement were classifiedas complying with the protocol. On the basis of these data,members of the clinic research staff initiated individualizedmeasures, as necessary, to increase compliance.
Colonoscopy
The study protocol specified that follow-up colonoscopy be performedtwice after the initial qualifying colonoscopy. The first colonoscopywas to take place one year after randomization (to identifyand remove adenomas missed at the qualifying colonoscopy), andthe second two years thereafter. However, the national recommendationsregarding the frequency of colonoscopic surveillance of patientswith a history of colorectal adenomas changed during the studyfrom one and three years after the initial resection to threeyears after resection.24,25,26 Thus, there was a decrease inthe rate of colonoscopy at one year among subjects enrolledin the latter part of the trial.
Data Collection
Results of endoscopy and pathological analysis were collectedfor each colonoscopy reported during the study. Using standardizedguidelines, we abstracted data on the completeness of the examinationand on the location, size, and histologic features of any resectedadenomas.
Complete blood counts and blood chemical analyses were performedduring screening and during the run-in phase of the study andannually thereafter. Diet was assessed according to the sameschedule with use of the Arizona Food-Frequency Questionnaire,which has been evaluated with respect to reliability and validityin this population.27 Information on adverse events was obtainedevery three months at the time the dietary supplement was dispensed.
Statistical Analysis
The original trial design and approach to analysis were describedin detail by Emerson et al.28 The target sample size of 1400subjects was based on a three-year rate of recurrence of adenomasof 40 percent and on an estimate that 10 to 15 percent of adenomaswould be missed during the colonoscopy at base line. Given apredicted dropout rate of 25 percent over a period of threeyears, we estimated that 950 subjects would complete the intervention.Given this sample size, the study had a statistical power of0.82 to detect a 25 percent reduction in the recurrence of adenomasand a power of 0.94 to detect a 30 percent reduction.
An interim analysis conducted in the latter part of the studysuggested a difference between groups in the proportion of subjectswho stopped taking the assigned supplement: 12.7 percent stoppedin the low-fiber group, and 23.3 percent stopped in the high-fibergroup. Therefore, for the remainder of the accrual period, theoriginal 1:1 schedule of randomization was changed to 4:1, withfour subjects assigned to the high-fiber group for every oneassigned to the low-fiber group.
We counted all adenomas, whether detected during the first colonoscopy(at year 1) or subsequent colonoscopic examinations. Subjectsin whom an adenoma was found during the one-year colonoscopywere not withdrawn from the study. Two separate analyses wereperformed. The first included all subjects who underwent colonoscopyone or more times after randomization, with recurrence definedas the identification of one or more adenomas after randomization.The second set of analyses included only subjects who underwentcolonoscopy at one year and one or more times thereafter. Recurrencewas defined for these analyses as the identification of anyadenoma after the one-year colonoscopy. Differences betweenthe high-fiber group and the low-fiber group in the rates ofcolonoscopy at one year and during follow-up were analyzed withthe use of chi-square tests, and the difference between thegroups in the length of time from randomization to the lastcolonoscopy was assessed with a log-rank test. Differences incharacteristics and in the incidence of adverse events amongpatients with recurrent adenomas in the two groups were testedwith chi-square tests.
Multivariate adjustment to test for an effect of wheat-branfiber was initially performed with the use of logistic regression(presence vs. absence of an adenoma). We used generalized estimatingequations with a Poisson link function to model the number ofrecurrent adenomas at each colonoscopy, adjusting for the timingof colonoscopy and assuming an exchangeable correlation structureamong the repeated procedures.29 Generalized estimating equationswere used to estimate the adjusted relative risk of the recurrenceof adenomas for the high-fiber group as compared with the low-fibergroup, whereas logistic regression was used to estimate theadjusted odds ratio (as an estimate of the adjusted relativerisk). Initial models fitted to test the effect of group assignmentwere adjusted only for the randomization period. Subsequentstatistical modeling also adjusted for sex and the number ofadenomas at the base-line colonoscopy (both of which are strongpredictors of the risk of recurrence) and factors that werefound to be significantly different between groups at base line.The significance of the treatment effect was assessed with theWald statistic.
Results
Enrollment and Randomization
We identified 4705 potentially eligible subjects. Of these,2088 declined to participate, 1006 were found to be ineligible,and 102 dropped out before the run-in phase. The remaining 1509subjects entered the six-week run-in phase, which consistedof the daily intake of a supplement low in wheat-bran fiber(2 g per day). Of the 3699 eligible subjects, 1429 (38.6 percent)successfully completed the run-in period and underwent randomization,627 to the low-fiber group and 802 to the high-fiber group.
Base-Line Characteristics of the Subjects
Table 1 shows the base-line characteristics of all 1429 randomizedsubjects and of the 1303 subjects (91.2 percent) who completedthe study by undergoing at least one colonoscopy after randomization.Of these 1303 subjects, 138 underwent only the one-year colonoscopy.The results for all randomized subjects who underwent colonoscopyafter randomization were included in an intention-to-treat analysis.
Table 1. Base-Line Characteristics of the Subjects.
Compliance
We assessed compliance with the dietary-supplement regimen bytwo methods: a count of cereal boxes returned to the study sitesand a calendar record of consumption kept by each subject. Withthe exception of the first year of the study, there was a significantdifference in compliance between the two groups (Table 2): theproportion of subjects who consumed more than 75 percent ofthe cereal supplement was lower in the high-fiber group thanin the low-fiber group (P<0.05). Counts of returned boxesindicated that compliance declined with each year of the study,so that by the third year, 84 percent of the low-fiber groupand 74 percent of the high-fiber group were consuming more than75 percent of the supplement. On the basis of responses to theArizona Food-Frequency Questionnaire, which includes intakeof fiber from the wheat-branfiber supplement and othersources, the mean total intake of fiber was 27.5 g per day inthe high-fiber group and 18.1 g per day in the low-fiber group.
Table 2. Self-Reported Compliance with the Protocol among the 1303 Subjects Who Completed the Study.
Recurrence of Adenomas
As noted in the Methods section, we changed the randomizationscheme during the latter part of the study. As a result, 276of the 1303 subjects underwent randomization according to a4:1 ratio (high fiber to low fiber) (Table 3). We did not detectsignificant differences between the high-fiber and low-fibergroups in the number of colonoscopic procedures performed amongsubjects who underwent randomization according to either theinitial 1:1 scheme or the 4:1 subsequent scheme; however, subjectswho underwent randomization during the later period underwentsignificantly fewer colonoscopic examinations during year 1than those who underwent randomization during the initial period.This difference clearly resulted from the change in clinicalscreening practice.
Table 3. Number of Colonoscopic Examinations after Randomization, According to Treatment Group and Randomization Scheme.
Table 4 shows the rates of recurrent adenomas among the 1303subjects who completed the study. The median observation periodwas 34 months in the high-fiber group and 36 months in the low-fibergroup (P=0.006). By the time of the last follow-up colonoscopy,the percentage of subjects with one or more recurrent adenomaswas 51.2 percent in the low-fiber group and 47.0 percent inthe high-fiber group (P=0.13). After adjustment for the randomizationscheme used, the odds ratio for the presence of at least onerecurrent adenoma in the high-fiber group, as compared withthe low-fiber group, was 0.88 (95 percent confidence interval,0.70 to 1.11; P=0.28).
When the analysis was restricted to the 889 subjects who underwentboth a one-year colonoscopy and another examination two yearslater, the recurrence rates in the high-fiber and low-fibergroups were not significantly different. With the use of generalizedestimating equations, the relative risk in the high-fiber group,as compared with the low-fiber group, was 0.99 (95 percent confidenceinterval, 0.71 to 1.36; P=0.93) for all 1303 subjects and 1.08(95 percent confidence interval, 0.71 to 1.64; P=0.73) for the889 subjects who underwent colonoscopy during year 1. Additionaladjustments for sex, the number of colonoscopic examinations,the number of adenomas found at the base-line colonoscopy, andbase-line variables that differed significantly between treatmentgroups did not change the results. Separate analyses revealedno significant differences in the rates of recurrence betweenwomen in the low-fiber group and women in the high-fiber group(40.7 percent vs. 40.8 percent, P=0.99). Among the men, therewere fewer recurrent adenomas in the high-fiber group than inthe low-fiber group (50.0 percent vs. 56.6 percent); this differencewas of borderline statistical significance (P=0.05). There wasno evidence of an effect of supplementation with wheat-branfiber among male subjects who underwent colonoscopy during thefirst year.
When we assessed the characteristics of the recurrent adenomas(Table 5), there was no significant difference between the twogroups regarding the size of the adenomas (P=0.71) or theirhistologic appearance (P=0.51). However, there was a significantlyhigher proportion of subjects with three or more recurrent adenomasin the high-fiber group than in the low-fiber group (P=0.03).When subjects were classified according to the sites of therecurrent adenomas (proximal colon or distal colon and rectumor both), the high-fiber and low-fiber groups were significantlydifferent (P=0.004); this result was largely due to the highernumber of subjects in the high-fiber group who had recurrentadenomas in both the proximal colon and distal colon and rectum.
Table 5. Characteristics of Adenomas Identified after Randomization among Subjects with Recurrent Adenomas.
Adverse Events
During the course of the study, nine cases of colorectal cancerwere reported, two in the low-fiber group and seven in the high-fibergroup (P=0.20). As shown in Table 6, among the 1303 subjectswho completed the study, there were 23 deaths: 10 in the low-fibergroup and 13 in the high-fiber group. There were no significantdifferences between groups in the occurrence of extracoloniccancer (P=0.58), cardiovascular disease (P=0.37), or stroke(P=0.69). The number of subjects who reported gastrointestinaleffects was significantly higher in the high-fiber group thanin the low-fiber group for all effects except constipation (Table 6).Most of these adverse effects were mild.
Table 6. Incidence of Death and Other Adverse Events after Randomization.
Discussion
In this double-blind trial, we found that a dietary supplementof wheat-bran fiber had no statistically significant protectiveeffect against recurrent colorectal adenomas. This finding wasunchanged whether the analysis was based on all colonoscopicprocedures performed after randomization or only those performedafter one year in the study. This method of analysis has beenused in other intervention studies of recurrent colorectal adenoma.30Moreover, the high-dose supplement of wheat-bran fiber had noeffect on the number of recurrent adenomas in subjects who hada recurrence. Our results are consistent with those of the TorontoPolyp Prevention Trial19 and the Australian Polyp PreventionProject.20 Although our secondary analyses suggested an effectof the high-fiber supplement among men, this result probablyrepresents a chance finding; in the Toronto Polyp PreventionTrial the effect of a low-fat, high-fiber diet was greater amongwomen than men.19 Furthermore, contrary to the findings of theAustralian trial, we did not see any evidence that the high-fibersupplement we used reduced the rate of recurrence of large adenomas.We observed no protective effect of the high-fiber supplementon the number, location, or histologic features of the recurrentadenomas. The combination of these observations argues againstthe idea that dietary supplementation with wheat-bran fibercan protect against recurrent colorectal adenomas. As reportedin this issue of the Journal, Schatzkin et al. found that alow-fat, high-fiber diet also failed to lower the risk of recurrenceof colorectal adenomas.31
We observed a relatively high rate of recurrent adenomas inthe proximal colon in both the low-fiber group and the high-fibergroup (48.2 percent and 41.4 percent, as compared with respectiverates of 26.4 percent and 27.5 percent at base line). When ratesof recurrent adenomas in the proximal colon are added to therates of recurrence occurring in both the proximal colon andthe distal colon or rectum, 68.2 percent of the subjects inthe low-fiber group and 74.0 percent of those in the high-fibergroup had recurrences in the proximal colon. The high ratesof recurrent adenomas in the proximal colon strongly suggestthat colonoscopy, rather than sigmoidoscopy, is the preferredmethod of surveillance, especially in patients with a historyof adenoma in the proximal colon.
In large, randomized clinical trials, randomization is expectedto result in a relatively equal distribution of subjects withrespect to risk factors of interest. In our trial, there wasa balanced distribution with respect to base-line age and sex,but imbalances in terms of exposure to tobacco, alcohol consumption,and total intake of fat. Nevertheless, the multivariate logistic-regressionanalysis, after adjustment for randomization period, sex, smokingstatus, alcohol consumption, and energy intake, did not showa significant effect of supplementation with wheat-bran fiberon the recurrence of colorectal adenomas. Thus, our resultsdo not appear to be related to an imbalance in the base-linecharacteristics of the subjects or to the change in the randomizationscheme from a 1:1 ratio to a 4:1 ratio in favor of the high-fibergroup.
Our experience underscores the difficulty of performing large-scalenutritional intervention trials, in terms of both recruitmentand compliance with the protocol. Of 3699 eligible subjects,1303 (35.2 percent) successfully completed the trial. In addition,by the third year of the study, only 74 percent of the subjectsin the high-fiber group, as compared with 84 percent of thosein the low-fiber group, consumed more than 75 percent of theirsupplemental cereal on a daily basis (a level we defined asindicative of compliance). Despite these difficulties, the meanintake of total fiber was 27.5 g per day in the high-fiber groupand 18.1 g per day in the low-fiber group. It can be arguedthat this level of intake over a period of three years is inadequateto prevent recurrent adenomas; however, our compliance dataindicate that higher daily consumption of wheat-bran fiber forlonger periods is not practical in adults older than 65 yearsof age.
The lack of effect of three years of supplementation with wheat-branfiber may reflect inadequate follow-up: three years may be tooshort. It could be argued that the total amount of dietary andcereal fiber consumed by the subjects in the high-fiber groupwas insufficient to protect against recurrent adenomas. It isalso possible that a high-fiber diet may be beneficial onlyin persons with lower base-line intakes of total fiber thanthose in our study. Alternatively, the use of wheat-branfibersupplements may only protect against the progression of largeadenomas to carcinomas. However, both the Nurses' Health Study15and the Health Professionals' Follow-up Study16 failed to findthat cereal fiber prevents colon cancer. Since cereal fiberhas potentially healthful effects in the prevention of coronaryheart disease,32,33 public health recommendations34,35 thatemphasize increased consumption of complex carbohydrates, whole-grainfoods, and cereal products may nevertheless be appropriate.
Supported in part by Public Health Service grants (CA-41108and CA-23074) from the National Cancer Institute and by theKellogg Company. Dr. Martínez was supported by a CareerDevelopment Award (KO1 CA79069-10) from the National CancerInstitute. The contents of this article are solely the responsibilityof the authors and do not necessarily represent the officialviews of the National Cancer Institute.
We are indebted to Dr. Victor Fulgoni (formerly of Kellogg)for his constant support; to Dr. Lee Sechrest, Lisa Hess, EllenGraver, and Kathleen Woolf for their expert advice concerningcompliance and dietary assessment; to Dr. William Stini formeasurement of bone mineralization; to Drs. Mikel Aickin andDaniel McGee for their advice concerning biostatistical designand analysis; and to Nancy Mason-Liddil, Evelyn Anthony, AnneDeJong-Ruhnau, and Roberta Graham for their tireless effortsin the day-to-day performance of the trial.
* The members of the Phoenix Colon Cancer Prevention Physicians'Network are listed in the Appendix.
Source Information
From the Arizona Cancer Center (D.S.A., M.E.M., D.J.R., J.M.G.-R., J.R.M., J.B.L., M.E.R.), the College of Public Health (D.S.A., M.E.M., D.J.R., J.R.M., M.E.R.), and the Departments of Pathology (A.B.B.) and Medicine (D.S.A., D.L.E., R.E.S.), University of Arizona, Tucson; the Center for Health Research, Portland, Oreg. (C.R.); the Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock (P.A.V.); and Veterans Affairs Medical Center, Tucson, Ariz. (R.E.S.). Other authors were Dianne Parish, B.S., Kris Koonce, B.S., and Lianne Fales, M.P.H., Arizona Cancer Center, University of Arizona, Tucson.Presented in abstract form at the 91st annual meeting of the American Association for Cancer Research, San Francisco, April 15, 2000.
Address reprint requests to Dr. Alberts at the Arizona Cancer Center, P.O. Box 245024, Tucson, AZ 85724-5024, or at dalberts{at}azcc.arizona.edu.
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Appendix
The members of the Phoenix Colon Cancer Prevention Physicians'Network were as follows: M. Cohen, P.G. Foutch, R.T. McDermott,Jr., R. Sawyer, Jr., A. Toraya, B. MacCollum, C. Stein, D. Meline,D. Wadas, D. Douglas, D.H. Winston, D. Johnson, D. Larson, D.-S.Cho, E.I. Leff, E. Cooper, E.I. Alper, F. Ramirez, F. Lewkowitz,F.J. Kogan, G. Severino, G. Burdick, J. Patel, J. Burgess, J.Kirkpatrick, J. Shaver, J. Singer, J. Mellen, J. Bickel, J.E.Phelps, J. Hanigsberg, J. Harlan, J. Mueller, J. Murphy, J.Leighton, K.S. Venkatesh, K. Parent, L. Pass, L.A. Bettinger,L. Rigberg, L. Shields, M.E. Harrison, M. Goldblatt, M. Hoefer,M. Shaukat, M. Altman, M. Rock, M. Schwimmer, M. Shapiro, M.Yanish, M. Anderson, P.S. Ramanujam, P.J. Berggreen, P. Kumar,R. Keate, R. Shah, R. Brooks, R. Jonas, R. Manch, R.J. Spencer,R. Leon, R. Sanowski, R. Heigh, S. Bellapravalu, S. Brown, S.Glouberman, S. Winograd, S. Kanner, V. Sartor, F. Taylor (deceased);Data and Safety Monitoring Committee E.R. Greenberg(Norris Cotton Cancer Center, Hanover, N.H.), R. Prentice (FredHutchinson Cancer Center, Seattle), E. Gritz (M.D. AndersonCancer Center, Houston), R. Haile (Norris Comprehensive CancerCenter, Los Angeles).
Ashbeck, E. L., Jacobs, E. T., Martinez, M. E., Gerner, E. W., Lance, P., Thompson, P. A.
(2009). Components of Metabolic Syndrome and Metachronous Colorectal Neoplasia. Cancer Epidemiol. Biomarkers Prev.
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