The Effect of Fecal Occult-Blood Screening on the Incidence of Colorectal Cancer
Jack S. Mandel, Ph.D., M.P.H., Timothy R. Church, Ph.D., John H. Bond, M.D., Fred Ederer, M.A., Mindy S. Geisser, M.S., Steven J. Mongin, M.S., Dale C. Snover, M.D., and Leonard M. Schuman, M.D.
Background Both annual testing for fecal occult blood and biennialtesting significantly reduce mortality from colorectal cancer.However, the effect of screening on the incidence of colorectalcancer remains uncertain, despite the diagnosis and removalof precancerous lesions in many persons who undergo screening.
Methods We have followed the participants in the Minnesota ColonCancer Control Study for 18 years. A total of 46,551 people,most of whom were 50 to 80 years old, were enrolled between1975 and 1978 and randomly assigned to annual screening, biennialscreening, or usual care (the control group). Those assignedto the screening groups were asked to prepare and submit twosamples from each of three consecutive stools for guaiac-basedtesting. Those with at least one positive slide in the set ofsix were offered a diagnostic examination that included colonoscopy.Screening was conducted between 1976 and 1982 and again between1986 and 1992. Study participants have been followed with respectto newly diagnosed cases of colorectal cancer and deaths. Follow-uphas been more than 90 percent complete.
Results During the 18-year follow-up period, we identified 1359new cases of colorectal cancer: 417 in the annual-screeninggroup, 435 in the biennial-screening group, and 507 in the controlgroup. The cumulative incidence ratios for colorectal cancerin the screening groups as compared with the control group were0.80 (95 percent confidence interval, 0.70 to 0.90) and 0.83(95 percent confidence interval, 0.73 to 0.94) for the annual-screeningand biennial-screening groups, respectively. For both screeninggroups, the number of positive slides was associated with thepositive predictive value both for colorectal cancer and foradenomatous polyps at least 1 cm in diameter.
Conclusions The use of either annual or biennial fecal occult-bloodtesting significantly reduces the incidence of colorectal cancer.
Three randomized, controlled clinical trials have shown thatboth annual screening and biennial screening for occult bloodin the stool significantly reduce the rate of death from colorectalcancer.1,2,3,4 Several observational studies have had similarresults.5,6,7,8,9,10,11,12,13 The reduction in mortality isevidently a consequence of the earlier detection and surgicalremoval of malignant colorectal tumors. Fecal occult-blood screeningmay yield an additional benefit: a reduction in the incidenceof colorectal cancer, resulting from the detection and removalof premalignant adenomatous polyps. Fecal occult-blood testsare not very sensitive for the presence of polyps but will detectsome, particularly large polyps, which are more likely to bleed14,15,16and also to become cancerous.17
Subjects in the National Polyp Study had a lower incidence ofcolorectal cancer than subjects in three historical controlgroups, which suggests that the incidence of this cancer isreduced by colonoscopic polypectomy and surveillance of personswith adenomatous polyps.18 In the trials of fecal occult-bloodscreening, many polyps were detected and removed during bowelexamination after a positive screening test. Thus, a reductionin the incidence of colorectal cancer in the screened groupsmight be expected. After 13 years of follow-up in the MinnesotaColon Cancer Control Study, the incidence of colorectal cancerwas 12 percent lower in the screened groups than in the controlgroups (P not significant).1 We now present data on the cumulativeincidence of colorectal cancer after 18 years of follow-up.
Methods
Participants
The Minnesota study was a randomized, controlled clinical trialconducted to evaluate the effectiveness of fecal occult-bloodtesting in reducing the rate of death from colorectal cancer.1,19Briefly, 46,551 people, the majority of whom were 50 to 80 yearsold when recruited between 1975 and 1978, were randomly assignedto annual screening, biennial screening, or usual care (controlgroup). The annual-screening and biennial-screening groups willbe referred to collectively as the screening groups. For eachscreening, participants assigned to the screening groups wereasked to prepare two guaiac-impregnated paper slides (Hemoccult,Beckman Coulter, Palo Alto, Calif.) for each of three consecutivestools and submit them to the investigators. Screening was conductedbetween 1976 and 1982 and, after a hiatus, resumed in 1986.All screening was completed in 1992.
The institutional review board of the University of Minnesotareviewed and approved the study, and all participants gave writteninformed consent.
Study Design
Participants with at least one positive slide were invited toundergo a diagnostic evaluation, which initially included historytaking and a physical examination, single-column barium enema,rigid proctosigmoidoscopy, urinalysis, a complete blood count,routine tests of blood chemistry, an upper gastrointestinalx-ray series, chest radiography, electrocardiography, and colonoscopy.Single-column barium enema was discontinued in 1978. Double-contrastbarium enemas were administered to participants who had at leastone positive screening test and whose colonoscopic examinationswere incomplete or suboptimal (about 5 percent of the subjects).Rigid proctosigmoidoscopy and the upper gastrointestinal serieswere discontinued in 1982. Throughout the trial, colonoscopywas the dominant diagnostic procedure used to identify colorectalpolyps and cancers. During colonoscopy, all polyps detectedwere routinely resected.
Diagnostic evaluation of subjects with positive screening testswas completed in 1993. Follow-up has continued to the presenttime in order to ascertain the incidence of colorectal cancerand all deaths.
Beginning in 1976 and continuing to the present, all study participantsreceived an annual questionnaire designed to ascertain vitalstatus and identify newly diagnosed colorectal polyps and cancersin the control group and in members of the screening groupswhose lesions were not detected by screening. Colorectal cancersreported in all three groups were confirmed by a review of relevantmedical records from the diagnosing or treating physicians orhospitals, with the written consent of the participants. Forcolorectal cancers and for polyps reported in conjunction withcolorectal cancers, slides of tissue were obtained for independentconfirmation and staging by the study pathologist.
To validate the method of ascertainment, new cases of colorectalcancer were also identified by linkage of the cohort, from 1988(the first year for which data were available) through 1994(the last year for which data were available), to the MinnesotaCancer Surveillance System,20 which collects data on all newlydiagnosed and pathologically confirmed cancers in Minnesota.
For deaths occurring in the first 15 years after enrollmentin the study, a deaths review committee, whose members had noknowledge of the group assignments, reviewed all records ofselected subjects who had died to determine the underlying causeof death. Included in this review were all such subjects inwhom a history of gastrointestinal disease or cancer could notbe definitively ruled out.21
Statistical Analysis
For the analysis of incidence, which included all cases diagnosedin the first 18 years of the study that were logged into thedata base before January 1, 1999, the cumulative probabilityof survival free of colorectal cancer was estimated by the life-tablemethod.22 The cumulative incidence was obtained by subtractingthis probability from 1. The 106 subjects in whom colorectalcancer was diagnosed before randomization were omitted fromthe analysis of incidence, leaving 46,445 subjects. The ratiosof the 18-year cumulative incidence of colorectal cancer inthe two screening groups to the incidence in the control groupand the 95 percent confidence intervals for these ratios werecomputed as a measure of the extent to which screening affectedincidence. Reported P values are two-sided, and no correctionwas made for multiple tests.
To evaluate the sensitivity of the fecal occult-blood test forthe detection of large polyps, we used the following indirectmethod.23 For all returned slide sets that contained all sixspecimens, the positive predictive value (for colorectal cancer,the fraction of subjects with a positive screening test whohad colorectal cancer; for polyps, the fraction who had polyps)was estimated for each given number of positive slides. Thepositive predictive value was calculated in the screening groupsseparately and for each of two outcomes: colorectal cancer orpolyps at least 1 cm in diameter but no colorectal cancer. Onlypositive tests that were followed by adequate examinations,defined as colonoscopy or a combination of flexible sigmoidoscopyand barium-enema radiography, were used in the computations.
To account for the potential correlation between repeated screeningsin the same subject, we estimated the positive predictive valueof each number of positive slides and for each screening groupin a single, generalized linear model with a logit-link function,using the generalized-estimating-equation approach.24,25,26,27Accounting for correlation in this manner corrects for the excessiveweight that would be given to participants with multiple screeningsif the positive predictive value were estimated as the simpleratio of the number of true positives to the total number ofpositive screening tests. Spearman's rho test28,29 was usedto measure the size and statistical significance of the associationbetween the number of positive slides and the positive predictivevalue.
Results
A total of 46,445 people (22,323 men and 24,122 women) withouta prior diagnosis of colorectal cancer were randomly assignedto one of the three study groups (Table 1). During the screeningperiod, participants in the annual-screening and biennial-screeninggroups were offered 11 and 6 opportunities for screening, respectively.The mean rate of compliance per screening opportunity was 75percent in the annual-screening group and 78 percent in thebiennial-screening group. Of the subjects with a positive test,83 percent in the annual-screening group and 84 percent in thebiennial-screening group underwent diagnostic follow-up, includinga complete examination of the large bowel by colonoscopy orthe combination of double-contrast barium enema and flexiblesigmoidoscopy. In each group, about 11 percent of the subjectswith positive screening tests underwent flexible sigmoidoscopyor barium enema or underwent another fecal occult-blood test.Five percent of the subjects with positive tests declined toconsult a physician. Overall, 75 percent of the subjects withpositive screening tests were examined at the University ofMinnesota Hospital and Clinics.
Table 1. Results of Fecal Occult-Blood Testing According to Study Group after 18 Years of Follow-up.
Follow-up for vital status through year 18 was complete for91.3 percent, 91.7 percent, and 91.2 percent of participantsin the annual-screening, biennial-screening, and control groups,respectively, and it was 95 percent complete through year 17for all groups. Death certificates were obtained for all but3 of the 15,873 people who were known to have died during the18-year follow-up period. Because active surveillance has continuedsince the cessation of screening, including a successful linkagewith the Minnesota Cancer Surveillance System (performed withoutknowledge of group assignment), the ascertainment of the incidenceof colorectal cancer was nearly complete and did not vary significantlybetween the groups.
During the 18 years of follow-up, approximately 235,000 person-yearswere accrued for each study group, and 1359 new cases of colorectalcancer were ascertained: 417 in the annual-screening group,435 in the biennial-screening group, and 507 in the controlgroup (Table 1 and Figure 1). The ratios of the cumulative incidencerates in the screening groups to that in the control group were0.80 (95 percent confidence interval, 0.70 to 0.90; P<0.001)for the annual-screening group and 0.83 (95 percent confidenceinterval, 0.73 to 0.94; P=0.002) in the biennial-screening group(Table 1).
Figure 1. Cumulative Incidence of Colorectal Cancer, According to Study Group, during 18 Years of Follow-up.
Table 2 shows the positive predictive value of a positive test,according to the number of positive slides, for colorectal cancerand for adenomatous polyps at least 1 cm in diameter but nocolorectal cancer. For both screening groups, there was a strongassociation between the number of positive slides and the percentageof subjects with colorectal cancer. For the annual-screeninggroup, the positive predictive value ranged from 0.87 percentfor one positive slide to 4.53 percent for six positive slides(Spearman's rho= 0.94, P=0.02). For the biennial-screening group,the positive predictive value ranged from 1.12 percent for onepositive slide to 6.13 percent for six positive slides (Spearman'srho=0.94, P=0.02). For adenomatous polyps at least 1 cm in diameter,there was also an association between the number of positiveslides and the positive predictive value; this value rangedfrom 5.99 percent to 7.87 percent for the annual-screening group(Spearman's rho=0.94, P= 0.02) and from 6.86 percent to 10.08percent for the biennial-screening group (Spearman's rho=0.83,P=0.06).
Table 2. Predictive Value of Fecal Occult-Blood Testing According to the Number of Positive Slides.
Discussion
Our findings demonstrate a significant reduction in the incidenceof colorectal cancer after fecal occult-blood testing. Thisreduction occurred after both annual and biennial screening.The most plausible explanation is the identification and removalof the precursor lesions for colorectal cancer thatis, adenomatous polyps. In study participants who were examinedat the University of Minnesota, polyps visualized during theexamination were routinely removed. For patients with a positiveslide who were examined elsewhere, the information on whetherpolyps were diagnosed and removed during follow-up was complete.However, the decision to remove polyps was made less consistentlythan at the University of Minnesota, especially during the earlyyears of the study. Since the focus of the study was on colorectalcancer, information was abstracted only on polyps that wereremoved in the course of a diagnosis of cancer or a workup aftera positive fecal occult-blood test. Thus, the attribution ofthe reduced incidence of colorectal cancer to the removal ofadenomatous polyps is based on the not unreasonable assumptionthat the removal of polyps was much more common in the screeninggroups than in the control group. The National Polyp Study foundthat the removal of adenomatous polyps, followed by colonoscopicsurveillance, significantly reduced the incidence of colorectalcancer below the rates in the general population.18 The sensitivityof fecal occult-blood tests for the detection of adenomatouspolyps has been reported to be moderate but is greater for largerpolyps, which are more likely to bleed, than for smaller polyps.14,15,16,17The positive predictive value increased with the number of positiveslides in our study, which further supports the results of earlierstudies14,15,16,17; our findings also provide evidence thatpolyp removal is the likely explanation for the decrease inincidence.
The failure of screening for fecal occult blood to lead to aclinically significant reduction in the incidence of colorectalcancer after early follow-up in some studies might be interpretedas an argument against the hypothesis that most cancers arisefrom benign adenomatous polyps.30,31 Our study supports thetheory of the adenomacarcinoma sequence and emphasizesthe importance of detecting and resecting advanced adenomas.To date, however, the European trials have involved less follow-up,making it difficult to show a reduction in incidence with screening.Lang and Ransohoff argued that the reduction in mortality fromcolorectal cancer in our trial was largely the consequence ofchance detection of cancers as a result of many colonoscopiesperformed, rather than a result of the sensitivity of the fecaloccult-blood test.32 However, the reverse has been shown tobe true; that is, the reduced mortality resulted primarily fromthe sensitivity of the fecal occult-blood test, with chancedetection of cancer playing only a minor part.33 It may similarlybe argued that the reduced incidence of colorectal cancer inour trial is largely the result of the chance detection of nonbleedingadenomatous polyps by the many colonoscopies performed, ratherthan a result of the sensitivity of the fecal occult-blood testfor the detection of bleeding polyps. However, the fecal occult-bloodtest was sensitive for larger polyps, as shown by the statisticallysignificant association between the positive predictive valueof a test and the number of positive slides.
The reductions in the incidence of colorectal cancer that weobserved may underestimate the true reductions that could beachieved among persons who elect to participate fully in screening.Compliance with screening in our trial was less than complete,averaging about 75 percent for each screening occasion. About50 percent of the screening subjects participated in all thescreening tests they were offered; 10 percent participated innone.1 In addition, subjects in the control group were not preventedfrom undergoing screening through their personal physicians.Thus, noncompliance in the screening groups and participationin screening in the control group are likely to have attenuatedthe true effect. A hiatus in the screening program, which averaged4.5 years for the annual-screening group and 3.6 years for thebiennial-screening group, is likely to have further attenuatedthe effect.4 Although subjects in the screening groups may haveparticipated in some screening beyond that offered in the study,the data that were collected indicate that this occurred infrequently(data not shown). Finally, screening advances the date of diagnosisand thus leads to a temporary, artifactual increase in incidence.After screening ceases, this effect is diminished.
The use of either annual or biennial fecal occult-blood testingsignificantly reduces the incidence of colorectal cancer. Preventingcolorectal cancers reduces morbidity and is likely to improvethe cost effectiveness of screening for colorectal cancer byfecal occult-blood testing.
Supported by research contracts (N01-CB-95613, N01-CB-61005,N01-CB-53862, and R01CA65728) with the National Cancer Instituteand by a cooperative agreement with the Centers for DiseaseControl and Prevention through the Association of Schools ofPublic Health.
We are indebted to G. Mary Bradley, D. Engelhard, J. Cordes,and G. Watt for their contributions to this study.
Source Information
From Exponent, Menlo Park, Calif. (J.S.M.); the Divisions of Environmental and Occupational Health (T.R.C., M.S.G., S.J.M.), Biostatistics (F.E.), and Epidemiology (L.M.S.), School of Public Health, University of Minnesota, Minneapolis; the Minneapolis Veterans Affairs Hospital, Minneapolis (J.H.B.); the Emmes Corp., Potomac, Md. (F.E.); and Fairview Hospital, Minneapolis (D.C.S.).
Address reprint requests to Dr. Mandel at Exponent, 149 Commonwealth Dr., Menlo Park, CA 94025, or at jmandel{at}exponent.com.
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