Use of Colonoscopy to Screen Asymptomatic Adults for Colorectal Cancer
David A. Lieberman, M.D., David G. Weiss, Ph.D., John H. Bond, M.D., Dennis J. Ahnen, M.D., Harinder Garewal, M.D., Ph.D., Gregorio Chejfec, M.D., William V. Harford, M.D., Dawn Provenzale, M.D., Steve Sontag, M.D., Tom Schnell, M.D., Theodore E. Durbin, M.D., Doug B. Nelson, M.D., Steve L. Ewing, M.D., George Triadafilopoulos, M.D, Francisco C. Ramirez, M.D., John G. Lee, M.D, Judith F. Collins, M.D., M. Brian Fennerty, M.D., Tiina K. Johnston, Ed.M., Christopher L. Corless, M.D., Ph.D., Kenneth R. McQuaid, M.D., Richard E. Sampliner, M.D., Thomas G. Morales, M.D., Ronnie Fass, M.D., Robert Smith, M.D., Yogesh Maheshwari, M.D., for The Veterans Affairs Cooperative Study Group 380
Background and Methods The role of colonoscopy in screeningfor colorectal cancer is uncertain. At 13 Veterans Affairs medicalcenters, we performed colonoscopy to determine the prevalenceand location of advanced colonic neoplasms and the risk of advancedproximal neoplasia in asymptomatic patients (age range, 50 to75 years) with or without distal neoplasia. Advanced colonicneoplasia was defined as an adenoma that was 10 mm or more indiameter, a villous adenoma, an adenoma with high-grade dysplasia,or invasive cancer. In patients with more than one neoplasticlesion, classification was based on the most advanced lesion.
Results Of 17,732 patients screened for enrollment, 3196 wereenrolled; 3121 of the enrolled patients (97.7 percent) underwentcomplete examination of the colon. The mean age of the patientswas 62.9 years, and 96.8 percent were men. Colonoscopic examinationshowed one or more neoplastic lesions in 37.5 percent of thepatients, an adenoma with a diameter of at least 10 mm or avillous adenoma in 7.9 percent, an adenoma with high-grade dysplasiain 1.6 percent, and invasive cancer in 1.0 percent. Of the 1765patients with no polyps in the portion of the colon that wasdistal to the splenic flexure, 48 (2.7 percent) had advancedproximal neoplasms. Patients with large adenomas (10 mm) orsmall adenomas (<10 mm) in the distal colon were more likelyto have advanced proximal neoplasia than were patients withno distal adenomas (odds ratios, 3.4 [95 percent confidenceinterval, 1.8 to 6.5] and 2.6 [95 percent confidence interval,1.7 to 4.1], respectively). However, 52 percent of the 128 patientswith advanced proximal neoplasia had no distal adenomas.
Conclusions Colonoscopic screening can detect advanced colonicneoplasms in asymptomatic adults. Many of these neoplasms wouldnot be detected with sigmoidoscopy.
Colorectal cancer is the second leading cause of death in NorthAmerica. There is evidence that the rate of mortality from colorectalcancer can be reduced by screening asymptomatic persons at averagerisk, beginning at the age of 50 years.1,2,3,4,5 The PreventiveServices Task Force has endorsed screening with the use of afecal occult-blood test or sigmoidoscopy.6 Colonoscopy is generallyreserved for patients with positive results of screening testsor those with a higher-than-average risk of colorectal cancer.A multidisciplinary panel of experts has recommended that screeningwith colonoscopy be considered for persons at average risk.7Experience with colonoscopy as a primary screening procedurehas been limited to a few case series.8,9,10 There have beenno direct comparisons between examinations limited to the distalcolon and full colonoscopy to determine the potential additionalbenefit of a full examination in asymptomatic persons.
We conducted a study to determine risk factors for neoplasticlesions with a diameter of 10 mm or more in asymptomatic personsbetween the ages of 50 and 75 years. Patients enrolled in thestudy underwent colonoscopic examination, during which all polypoidlesions were removed and evaluated histologically. The purposeof the study was to determine the prevalence and location ofcolonic neoplasia in asymptomatic patients, the risk of proximaladvanced neoplasia in patients with and in those without neoplasiain the distal colon, and the likelihood that advanced proximalneoplasia would be detected on the basis of the presence ofan adenoma in the distal colon.
Methods
Patients
The study protocol was approved by a central human-rights committeeand by the corresponding committee at each participating center.Patients were enrolled in the study between February 1994 andJanuary 1997. They were recruited from 13 Veterans Affairs medicalcenters, representing each major region of the United States.Patients were recruited in one of three ways: by random selectionfrom the center's clinic list on the basis of age, by the selectionof asymptomatic patients referred for screening sigmoidoscopy,and by advertisement for patients with a family history of colorectalcancer. Oversampling for patients who had one or more first-degreerelatives with colorectal cancer was performed in order to havean adequate number of patients with a family history in thesample.
A study nurse asked each patient to complete a brief questionnairedesigned to determine eligibility for the study. Patients wereexcluded if they reported symptoms of lower gastrointestinaltract disease, including rectal bleeding, on more than one occasionin the previous six months, a marked change in bowel habits,or lower abdominal pain that would normally require medicalevaluation. Other exclusion criteria were current participationin other studies, a history of disease of the colon (colitis,polyps, or cancer) or colonic surgery, a colonic examinationwithin the previous 10 years (sigmoidoscopy, colonoscopy, orbarium enema), a medical condition that could increase the riskassociated with colonoscopy (active cardiac or pulmonary diseaseor other serious disease) or that would preclude a benefit fromcolonoscopic screening (cancer or any terminal illness), a prostheticheart valve, anticoagulant therapy, nonmedical problems (psychiatricdisorders, lack of transportation, homelessness or lack of supportat home, or excessive use of alcohol), and a need for specialprecautions in performing colonoscopy (i.e., antibiotic prophylaxis).In addition, women of childbearing potential were excluded.
Study Protocol
Eligible persons who provided informed consent completed detailedquestionnaires that covered diet, physical activity, drug use,and family history of cancer. A physical examination was performed,and laboratory studies were ordered to evaluate coagulation.The patients received a polyethylene glycolbased electrolytesolution for bowel preparation, along with instructions foruse. A complete colonoscopic examination was performed whilethe patients were under conscious sedation with an intravenousagent. All examinations were performed at the participatingcenters by the study investigators, who were selected becauseof their extensive experience with colonoscopy. During the examination,the location and size of all polypoid lesions were noted bystudy nurses. The size of each polyp was estimated with theuse of an open-biopsy forceps, which is 7 mm in diameter. Investigatorswere required to provide photographic documentation of cecallandmarks and of all polyps and other important lesions.
If the colonoscopic examination was incomplete because of problemswith bowel preparation or failure to reach the cecum, the patientwas asked to return for a second attempt. If a complete examinationwas performed within six months after the first attempt, a completeexamination was reported, and the combined results of the twoexaminations were included in the analysis. If the second examinationwas also incomplete, the results were excluded from the analysis.If the patient underwent surgery within six months after theinitial examination and if the resected specimen could be evaluated,then a complete examination was reported, and the results wereincluded in the analysis.
Histologic Evaluation
All retrieved polypoid lesions were sent to local pathologylaboratories for histologic evaluation. Slides were sent toa designated expert in pathology at the Veterans Affairs MedicalCenter in Hines, Illinois, for an independent, blinded review.When there was agreement between the local pathologist and thepathologist at the coordinating center, a final pathologicalclassification was made. When there was disagreement, the slideswere sent to a pathologist at the Veterans Affairs medical centerin Minneapolis or in Portland, Oregon. The results of the thirdreview were used to classify the lesion.
Patients were classified on the basis of their most advancedlesion in order to determine the prevalence of pathologicalfeatures. For example, a patient who had a villous adenoma anda tubular adenoma was classified as having a villous adenoma.The most advanced lesions in the entire colon, distal colon,and proximal colon were determined. Patients were classifiedseparately according to the number of adenomas in the distalcolon and the number in the entire colon. The distal colon wasdefined as the rectum, sigmoid, and descending colon up to butnot including the splenic flexure. The proximal colon was definedas the splenic flexure and other, more proximal portions ofthe colon. The risk of proximal neoplasia associated with distalcolonic lesions was determined.
Advanced colonic neoplasia was defined as an adenoma with adiameter of 10 mm or more, a villous adenoma (i.e., at least25 percent villous), an adenoma with high-grade dysplasia, orinvasive cancer. Patients with intramucosal carcinoma or carcinomain situ were classified as having high-grade dysplasia. Cancerwas defined as the invasion of malignant cells beyond the muscularismucosa.
Statistical Analysis
Data-base management and all statistical analyses were performedwith SAS software (SAS Institute, Cary, N.C.). Rates and proportionswere calculated for categorical data, and means and standarderrors for continuous data. In addition, standard logistic-regressionmethods were used to calculate odds ratios for advanced neoplasia,with 95 percent confidence intervals.11 Odds ratios were adjustedfor age and family history of cancer in analyses of the riskof advanced neoplasia in the distal and proximal colon.
Results
A total of 17,732 patients were screened for enrollment in thestudy, and 3196 eligible patients were enrolled. Selected demographiccharacteristics of the study population are shown in Table 1.The proportion of patients who were recruited by random selectionfrom clinic lists was 48.8 percent; 45.0 percent of the patientshad been referred for sigmoidoscopy, and 6.2 percent had respondedto the advertisement for patients with a family history of colorectalcancer. The prevalence of a family history of colorectal cancer(one or more affected first-degree relatives) was 13.9 percentin the final study population but 8.2 percent in the overallgroup of patients who were randomly selected from clinic patients,with the difference due to oversampling. The most frequentlyreported reasons for exclusion are shown in Table 2. A totalof 1463 patients met the criteria for enrollment but declinedto participate.
Colonoscopy was completed to the cecum in 3121 of the 3196 patients(97.7 percent). In 14 patients, more than one procedure wasrequired to complete the examination. Patients were classifiedon the basis of the most advanced lesion found in the colon(Table 3). A total of 1441 patients (46.2 percent) had no polypoidlesions. In the other 1680 patients (53.8 percent), a totalof 5218 polyps were removed. In 391 patients (12.5 percent),the most advanced lesions were hyperplastic polyps. In 118 patients(3.8 percent), biopsy of what appeared to be a polyp revealedeither normal mucosa or nonpolypoid, miscellaneous findings.In all, 62.5 percent of the patients had no evidence of neoplasia.
Table 3. Colonoscopic Findings According to the Most Advanced Lesion.
A total of 1171 patients had one or more adenomas of any typeor invasive cancer (37.5 percent). In 842 patients, the mostimportant finding was a tubular adenoma that was less than 10mm in diameter. Of these patients, 687 had one or two adenomas,112 had three or four, and 43 had five or more.
Advanced disease (defined as an adenoma with a diameter of atleast 10 mm, or villous features, high-grade dysplasia, or invasivecancer) was present in 329 patients (10.5 percent). In 155 patients(5.0 percent), the most advanced lesions were large tubularadenomas (10 mm). Ninety-three patients (3.0 percent) had adenomaswith villous features, 51 (1.6 percent) had adenomas with high-gradedysplasia, and 30 (1.0 percent) had invasive cancer. Among thepatients with cancer, the stage was T1N0 in nine patients, T2N0in six, and T3N0 in seven; six patients had nodal involvement(N1 or N2), and two had metastatic disease.
The most advanced lesions in the distal colon and in the proximalcolon were identified separately for each patient (Table 4).In the primary analysis, the distal colon was defined as therectum and the sigmoid and descending colon. According to thisdefinition, 228 patients (7.3 percent) had advanced diseasein the distal colon (i.e., distal to the splenic flexure) and128 (4.1 percent) had advanced disease in the proximal colon.We also determined the prevalence of advanced disease in thedistal colon defined as only the rectum and sigmoid colon. Withthe more restricted definition, 188 (6.0 percent) had advanceddisease in the distal colon, and 169 (5.4 percent) had advanceddisease in the proximal colon.
Table 4. Prevalence and Location of Advanced Neoplasia.
The likelihood that advanced proximal neoplasia would be detectedon examination of the distal colon was determined by notingthe presence or absence of an adenoma in the portion of thecolon that was distal to the splenic flexure (Table 4). Amongthe patients with advanced proximal neoplasia, 48.4 percent(62 of 128) had at least one adenoma in the distal colon, and14.1 percent (18 of 128) had large adenomas (10 mm in diameter)in the distal colon. With the distal colon defined as the rectumplus the sigmoid colon, only 37.9 percent of the patients withadvanced proximal neoplasia (64 of 169) had a distal adenoma.
Among the patients with no adenomas distal to the splenic flexure,2.7 percent had advanced proximal neoplasia. These patientsserved as the reference group in an analysis of the risk ofadvanced proximal neoplasia according to the distal findings.The odds ratios (with 95 percent confidence intervals), adjustedfor age and the presence or absence of a family history of colorectalcancer, are shown in Table 5, according to the two definitionsof the distal colon. The patients with distal hyperplastic polypsdid not have a higher risk of advanced proximal neoplasia thanthe patients without distal polyps. However, the patients withsmall or large adenomas in the distal colon had a significantlyincreased risk of advanced proximal neoplasia: odds ratio forpatients with small adenomas, 2.6 (95 percent confidence interval,1.7 to 4.1); odds ratio for patients with large adenomas, 3.4(95 percent confidence interval, 1.8 to 6.5). Among patientswith small tubular adenomas (<10 mm in diameter) in the distalcolon, the presence of one or two adenomas was significantlyassociated with an elevated risk of proximal advanced neoplasia,but the presence of a larger number of adenomas did not furtherincrease the risk. When the distal colon was defined as therectum and sigmoid colon, the presence of distal adenomas, whethersmall or large, was still associated with an increased riskof advanced proximal neoplasia. The odds ratio for proximaladvanced neoplasia was higher for the patients with distal villousadenomas (4.7; 95 percent confidence interval, 2.1 to 10.4)than for the patients with distal tubular adenomas (2.6; 95percent confidence interval, 1.7 to 4.0), but the differencewas not statistically significant.
Table 5. Risk of Advanced Proximal Neoplasia According to the Distal Findings.
The effect of age on the prevalence of advanced neoplasia wasassessed as an independent variable. The prevalence of advancedneoplasia increased from 5.7 percent in the youngest patients(50 to 59 years old) to 13 percent in the oldest patients (70to 75 years old). There was a trend toward an increased prevalenceof advanced proximal neoplasia with age (P<0.001): the prevalencewas 2 percent for patients who were 50 to 59 years old, 4.9percent for those 60 to 69 years old, and 5.9 percent for those70 to 75 years old.
There were no differences in the rates of advanced neoplasiaaccording to the method used to recruit patients (P=0.32). Patientswith a family history of colorectal cancer who were recruitedby any of the three methods had a higher age-adjusted risk ofadvanced neoplasia than patients with no family history (14.3percent vs. 9.9 percent; odds ratio, 1.5; 95 percent confidenceinterval, 1.1 to 2.0).
Ten patients (0.3 percent) had serious complications duringor immediately after colonoscopy: six patients had gastrointestinalbleeding that required hospitalization, and one each had a myocardialinfarction, a cerebrovascular accident, Fornier's gangrene thatrequired hospitalization, and thrombophlebitis. Three patientsdied within 30 days after colonoscopy; none of the deaths weredirectly related to the procedure. There were no perforations.
Discussion
We evaluated the use of colonoscopy as a primary screening procedurein a large number of asymptomatic adults. The combined prevalenceof invasive cancer and adenoma with high-grade dysplasia was2.6 percent. Most of the patients with cancer (73.3 percent)were identified before there was nodal involvement or distalspread and were therefore candidates for curative treatment.These data suggest that screening with colonoscopy in asymptomaticmen can detect early and potentially curable advanced neoplasia.In the National Polyp Study,12 patients who underwent colonoscopy,with the removal of all polyps, had a lower incidence of colorectalcancer during six years of follow-up than did the referencepopulations. Although our study was not designed to determinewhether colonoscopic screening would reduce the rate of mortalityfrom colorectal cancer, the results indicate that many casesof advanced neoplasia would be detected as part of a colonoscopicscreening program.
Our findings can be used to determine the yield of a screeningexamination limited to the distal colon. There has been controversyabout the importance of detecting small adenomas (<10 mmin diameter) in the distal colon.13,14,15,16,17,18,19 In ourstudy, all patients were asymptomatic and underwent full colonoscopy,irrespective of the findings in the distal colon. Patients withno polyps of any kind in the rectum or sigmoid or descendingcolon had a risk of advanced proximal neoplasia of 2.7 percent.Among patients with no polyps in the rectum or sigmoid colon,the prevalence of advanced proximal neoplasia was 3.7 percent.The risk of proximal advanced neoplasia increased significantlywith age. Patients with distal hyperplastic polyps had a riskof advanced proximal neoplasia that was similar to the riskamong patients with no polyps. However, patients with distaladenomas of any size had a higher risk of advanced proximalneoplasia than patients with no distal adenomas.
We determined the prevalence of advanced proximal neoplasiain asymptomatic patients and the likelihood that such patientswould have any adenomas in the distal colon (Table 4). Whenthe distal colon was defined as the rectum and the sigmoid anddescending colon, 48.4 percent of the patients with advancedproximal neoplasia had adenomas in the distal colon. When thedistal colon was defined as the rectum and sigmoid colon, only37.9 percent of the patients with proximal advanced neoplasiahad distal advanced neoplasia. Therefore, the majority of advancedproximal neoplasms would not have been detected if the distalcolon had been examined either to the junction of the sigmoidcolon and the descending colon or to the splenic flexure.
These data can be interpreted in two ways. Examination of thedistal colon to the splenic flexure, followed by full colonoscopyif an adenoma of any size had been found, would have identifiedthe 79.9 percent of patients with advanced neoplasia. However,if the distal colon had been examined only to the junction ofthe descending colon and the sigmoid colon, then the advancedneoplasia in 31.9 percent of the patients would not have beendetected. Failure to detect advanced neoplasia may be more likelyin older patients than in younger patients, since the prevalenceof advanced proximal disease increases with age.
Our study population included a disproportionately large numberof patients who had one or more first-degree relatives withcolorectal cancer. These patients had an increased age-adjustedrisk of advanced neoplasia, a finding that is consistent withthe results of other studies.20,21,22 These data support therecommendation of an expert panel that colonoscopy be offeredto such patients.7
Our study has several important limitations. First, the resultsare applicable only to men. There is considerable evidence thatmen have higher age-adjusted rates of cancer than women.23 Inaddition, a definition of the distal colon that includes theleft colon to the splenic flexure may not reflect the actualdepth of insertion of a sigmoidoscope. Therefore, we determinedthe yield of an examination that reached the junction of thesigmoid colon and the descending colon. Our data demonstratethat a more extensive examination of the colon leads to a higherrate of detection of advanced neoplasia. Finally, the effectivenessof colonoscopy depends on the expertise of the endoscopist.24In our study, all the endoscopists had substantial experiencewith colonoscopy, as reflected by the high rate of successfulcecal intubation. The results of examinations performed by lessexperienced endoscopists may be different.
We believe that the use of colonoscopy to screen asymptomaticmen for colorectal cancer is feasible and that such screeningcan identify patients with advanced neoplasia who may benefitfrom the detection and removal of the lesions. The majorityof advanced lesions are distal to the splenic flexure. However,our data show that more than half the cases of advanced proximalneoplasia would not be detected with sigmoidoscopy to the splenicflexure. Patients with distal adenomas of any size have a higherrisk of advanced proximal neoplasia than patients with no distaladenomas. In the group of patients in our study who had no distaladenomas, 2.7 percent had advanced proximal lesions, which wouldnot have been detected with sigmoidoscopy alone. It remainsto be determined whether a full colonic examination will leadto a greater reduction in the rate of mortality from colorectalcancer than other methods of screening.
Supported by a grant from the Veterans Affairs Cooperative StudiesProgram.
* Participants in the study group are listed in the Appendix.
Source Information
From the Veterans Affairs medical centers in Portland, Oreg. (D.A.L.); Perry Point, Md. (D.G.W.); Minneapolis (J.H.B.); Denver (D.J.A.); Tucson, Ariz. (H.G.); and Hines, Ill. (G.C.). Other authors were William V. Harford, M.D., Dallas; Dawn Provenzale, M.D., Durham, N.C.; Steve Sontag, M.D., and Tom Schnell, M.D., Hines, Ill.; Donald R. Campbell, M.D., Kansas City, Mo.; Theodore E. Durbin, M.D., Long Beach, Calif.; Doug B. Nelson, M.D., and Steve L. Ewing, M.D., Minneapolis; George Triadafilopoulos, M.D., Palo Alto, Calif.; Francisco C. Ramirez, M.D., Phoenix, Ariz.; John G. Lee, M.D., Judith F. Collins, M.D., M. Brian Fennerty, M.D., Tiina K. Johnston, Ed.M., and Christopher L. Corless, M.D., Ph.D., Portland, Oreg.; Kenneth R. McQuaid, M.D., San Francisco; Richard E. Sampliner, M.D., Thomas G. Morales, M.D., and Ronnie Fass, M.D., Tucson, Ariz.; and Robert Smith, M.D., and Yogesh Maheshwari, M.D., White River Junction, Vt. all at Veterans Affairs medical centers.
Address reprint requests to Dr. Lieberman at the Division of Gastroenterology, Oregon Health Sciences University, Portland Veterans Affairs Medical Center, P3-GI, P.O. Box 1034, Portland, OR 97207.
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Appendix
The following persons participated in Veterans Affairs StudyGroup 380: Data Monitoring Board B. Levin (chairman),C.R. Boland, M. Brown, R. Burt, R.B. D'Agostino, and D.K. Rex;Executive Committee S. Prindiville (special consultant,Denver), A. Schatzkin (Bethesda, Md.), W. Willett (Boston),and J.F. Collins (Perry Point, Md.); Planning Committee J. Selby and C. Quesenberry; Veterans Affairs Cooperative ProgramOffice J.R. Feussner, D. Deykin, and P. Huang.
Study personnel Dallas: M. Prebis; Denver: S. Frederickand B. Ciminelli; Durham, N.C.: C. Rose, M.J. Timmins, and R.Smith; Hines, Ill.: S. O'Connell; Kansas City, Mo.: R. Corbett;Long Beach, Calif.: S. Van Schoick, C. Nordin, E. Dumitrescu,B. Bagnol, and M. Du; Minneapolis: S. Schwartz; Palo Alto, Calif.:D. Tizer; Phoenix, Ariz.: R. Sanowski and S. Medlin; Portland,Oreg.: M. Garrard; San Francisco: S. Woodford; Tucson, Ariz.:P. Martinez; White River Junction, Vt.: L. Miraldi; study chairman'soffice M. Sutton; Veterans Affairs Cooperative StudiesProgram Coordinating Center B. Calvert, J. Collins,C. Crigler, M. Lee, R. Ortiz, and E. Spence; central laboratory(Tucson, Ariz.): L. Ramsey.
Screening for Colorectal Cancer
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Extract |
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N Engl J Med 2000;
343:1651-1654, Nov 30, 2000.
Correspondence
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