Evidence of Benefit
Fecal Occult Blood Test
Newer FOBTs: Nonrandomized Controlled Trial Evidence
Sigmoidoscopy
Combination of FOBT and Flexible Sigmoidoscopy
Barium Enema
Colonoscopy
Virtual Colonoscopy (Computed Tomographic Colonography)
Digital Rectal Examination
Detection of DNA Mutations in the Stool
Fecal Occult Blood Test
There are five controlled clinical trials that have been completed or that are in
progress to evaluate the efficacy of screening utilizing the fecal occult blood
test (FOBT). The Swedish trial is a targeted study for the group aged 60 to 64 years.[1] The English program selects candidates from lists of family
practitioners.[2] The Danish trial offers screening to a population aged 45
to 75 years randomly assigned to a control or study group.[3,4]
The Memorial Sloan-Kettering Cancer Center-Strang Clinic (MSKCC) trial,
completed in 1985, was an evaluation of the FOBT as a supplement to annual
rigid sigmoidoscopy.[5] The study and control groups were selected by calendar
periods.
The Minnesota trial demonstrated that annual FOBT testing using primarily
rehydrated samples decreased mortality from colorectal cancer (CRC) by 33% [6] and
that biennial testing developed a 21% relative mortality reduction.[7] A large part of the reduction may be attributed to chance
detection of cancer by colonoscopies; rehydration of guaiac test slides greatly
increased positivity and consequently increased the number of colonoscopies performed.[8]
Subsequent analyses by the Minnesota investigators using mathematical modeling
suggested that for 75% to 84% of the patients mortality reduction was achieved
because of sensitive detection of CRCs by the test; chance
detection played a minor role (16%–25% of the reduction).[9] Nearly 85% of
patients with a positive test underwent diagnostic procedures that included
colonoscopy or double-contrast barium enema plus flexible sigmoidoscopy (FS). After
18 years of follow-up, the incidence of CRC was reduced by 20% in
the annually screened arm and 17% in the biennially screened arm.[10]
The English trial allocated approximately 76,000 individuals to each arm.
Those in the screened arm were offered nonrehydrated FOBT testing every 2 years
for three to six rounds from 1985 to 1995. Median follow-up time was 7.8 years.
Sixty percent completed at least one test; 38% completed all tests. Cumulative
incidence of CRC was similar in both arms. The trial reported a
relative risk (RR) reduction of 15% in CRC mortality (odds ratio
[OR] = 0.85; 95% confidence interval [CI], 0.74–0.98).[11] In this study, the
serious complication rate of colonoscopy was 0.5%. There were five deaths within
30 days of surgery for screen-detected CRC or adenoma in a
total of 75,253 individuals screened.[12]
After a median follow-up of 11.8 years, a difference in CRC incidence between the intervention and control groups was not observed. Overall, the disease-specific mortality rate ratio associated with screening was 0.87 (0.78–0.97; P = .01). The rate ratio for death from all causes was 1.00 (0.98–1.02; P = .79).[13]
The Danish trial in Funen, Denmark, entered approximately 31,000 individuals
into two arms, in which individuals in the screened arm were offered
nonrehydrated FOBT testing every 2 years for nine rounds over a 17-year period.
Sixty-seven percent completed the first screen, and more than 90% of individuals
invited to each subsequent screen underwent FOBT testing. This trial
demonstrated an 18% reduction in CRC mortality at 10 years of
follow-up,[14] 15% at 13 years of follow-up (RR = 0.85; 95% CI,
0.73–1.00),[15] and 11% at 17 years of follow-up (RR = 0.89; 95% CI, 0.78–1.01).[16] CRC incidence and overall mortality was
virtually identical in both arms.
All trials have shown a more favorable stage distribution in the screened
population compared with controls (Table 3 1). Data from the Danish
trial indicate that while the cumulative incidence of CRC was
similar in the screened and control groups, a higher percentage of CRCs and adenomas were Dukes A and B lesions in the screened group.[14]
A meta-analysis of all previously reported randomized trials using biennial FOBT showed no overall mortality reduction by FOBT screening (RR = 1.002; 95% CI, 0.989–1.085). The RR of CRC death in the FOBT arm was 0.87 (95% CI, 0.8–0.95), and the RR of non-CRC death in the FOBT group was 1.02 (95% CI, 1.00–1.04; P = .015).[17]
The MSKCC study evaluated compliance and effectiveness, in a setting of
comprehensive medical examinations, of using the FOBT in conjunction with
sigmoidoscopy to screen for CRC. From 1975 to 1979, a total of
21,756 patients (aged 40 years and older) who presented at the Preventive Medicine
Institute-Strang Clinic for routine medical evaluations were enrolled by
calendar period into study and control groups. Study patients were offered
annually both rigid sigmoidoscopy examinations and FOBTs requiring two stool
specimens per day for 3 days, while control patients were offered only annual
sigmoidoscopy. Trial I was primarily a demonstration of feasibility of using
the FOBT as a supplemental screening method. Trial II was an evaluation of
effectiveness. In Trial II, CRC mortality was lower in the study
group than in the control group (0.36 vs. 0.63 per 1,000), a nonstatistically
significant result (P = .053).
Mathematical models have been constructed to extrapolate the results of
screening trials to screening programs for the general population in community
health care delivery settings. These models project a reduction in CRC mortality or an increase in life expectancy using currently available
screening methodology.[18-21] The anticipated success of such methodology is
critically dependent on the appropriate use of the FOBT and an effective
clinical management plan.[22,23]
A systematic review done through the Cochrane Collaboration examined all CRC screening randomized trials that involved FOBT testing on more than one occasion. The combined results showed that trial participants allocated to screening had a 16% lower CRC mortality (RR = 0.84; 95% CI, 0.78–0.90). There was, however, no difference in all-cause mortality between the screened and control groups (RR = 1.00; 95% CI, 0.99–1.02). Furthermore, the trials reported a low positive predictive value for the FOBT test, suggesting that more than 80% of all positive tests were false-positives.[24]
In a population-based pilot study in Finland, guaiac FOBT screening was judged to be impractical due to low specificity and its attendant costs.[25]
On initial (prevalence) examinations, from 1% to 5% of unselected
persons tested with FOBT have positive test results. Of those with positive
test results, approximately 2% to 10% have cancer and approximately 20% to 30%
have adenomas,[26,27] depending on how the test is done. Data from randomized
controlled trials are summarized in Table 3 1.
Table 3. Randomized Controlled Screening Trials: Fecal Occult Blood Testing
Site
|
Population Size
|
Positivity Rate (%)
|
% Localizeda
|
Testing Interval
|
Relative Mortality Reduction
|
a% Localized = T1–3 N0 M0.
|
|
Screened
|
Control
|
|
Minnesota [6,7] |
48,000 |
Unrehydrated: 2.4% |
59 |
53 |
Annual |
33% |
|
Rehydrated: 9.8% |
|
|
Biennial |
21% |
United
Kingdom [11]
|
150,000 |
Unrehydrated: 2.1% |
52 |
44 |
Biennial |
15% |
Denmark [14]
|
62,000 |
Unrehydrated: 1.0% |
56 |
48 |
Biennial |
18% |
Sweden [1] |
27,000 |
Unrehydrated: 1.9% |
65 |
33 |
|
Not
available |
|
Rehydrated: 5.8% |
|
|
|
|
Newer FOBTs: Nonrandomized Controlled Trial Evidence
Newer FOBTs have been developed to detect human hemoglobin (immunochemical FOBT [iFOBT]) in contrast to the peroxidase-like activity that is detected by the guaiac-based FOBT (gFOBT) studied in the randomized controlled trials above.
In a study of 1,000 persons at high risk of CRC and who had colonoscopy and iFOBT done on three bowel movements, the sensitivity and specificity for CRC was 94% and 87%; for advanced adenoma and CRC, it was 67% and 91%.The results were only slightly changed after removing seven patients with cancer who had been referred because of guaiac-positive FOBT or anemia.[28] In another study using a different iFOBT, tested in one bowel movement, the sensitivity for CRC was 66% and for advanced adenoma and CRC, the sensitivity was 27%; specificity was 95%.[29] These sensitivities are much higher than the 13% to 39% sensitivity for CRC using gFOBT when studied in a similar way. A systematic review of guaiac and immunochemical FOBTs commissioned to evaluate the comparative diagnostic performance of the two FOBT test types to inform a decision to introduce screening for CRC in the United Kingdom found no clear performance superiority of either type and significant sensitivity variability among types in different clinical settings.[30]
Sigmoidoscopy
The flexible fiberoptic sigmoidoscope was introduced in 1969. The 60 cm
flexible sigmoidoscope became available in 1976.[31] The flexible
sigmoidoscope permits a more complete examination of the distal colon with more
acceptable patient tolerance than the older rigid sigmoidoscope. The rigid instrument can discover 25% of polyps, and the 60 cm
scope can find as many as 65%. The finding of an adenoma by FS may
warrant colonoscopy to evaluate the more proximal portion of the colon.[32,33]
The prevalence of advanced proximal neoplasia is increased in patients with a
villous or tubulovillous adenoma distally and is also increased in those aged 65
years or older with a positive family history of CRC and with
multiple distal adenomas.[34] Removal of adenomas is associated with a
decreased risk of subsequent CRC.[35] While most of these
adenomas are polypoid, flat and depressed lesions may be more prevalent than
previously recognized. Large flat and depressed lesions are more likely to be
severely dysplastic. Specialized techniques may be needed to identify, biopsy,
and remove such lesions.[36]
Virtually all screening studies using these types of sigmoidoscopes have
demonstrated an increase in the proportion of early cases and a corresponding
increase in survival compared with cases diagnosed in a nonscreening environment.
Most of these studies, however, lack appropriate comparison groups, and their
interpretation is unclear because of screening biases.
The Memorial-Strang Clinic sigmoidoscopy study was conducted between 1946 and
1954 in 26,124 patients.[37] The survival rate in the 58 patients found to
have cancer was 90% after a follow-up period of 15 years. There were, however,
neither controls nor adjustment for biases.
One study was conducted over a 25-year period with 18,158 patients who
underwent periodic rigid sigmoidoscopy with removal of polyps.[38] This study
showed a significant reduction in the incidence of cancer in the rectosigmoid
colon when compared with statewide data. There were 14 rectal cancers in the
study group, which was only 15% of the expected incidence in that state. This study,
however, was not controlled and provided minimal follow-up data.
The Kaiser-Permanente Multiphasic Health Checkup was a randomized study of
10,713 health plan members between the ages of 35 and 54 years; after 16 years, the
study reported a more favorable stage distribution and survival rate and a
reduction in mortality between the study and control groups (12 vs. 29
deaths, respectively), which was statistically significant.[39] In a re-evaluation
considering only those cancers within reach of the sigmoidoscope, no
statistical difference, however, could be demonstrated.
Two case-control studies have been reported that evaluate the efficacy of
screening sigmoidoscopy in preventing CRC mortality;[40,41] one
study used rigid sigmoidoscopy, and the other used rigid and FS. Both
studies were conducted in prepaid health plans and suggested a significantly
decreased risk (70%–90%) of fatal cancer of the distal colon or rectum among
individuals with a history of one or more sigmoidoscopic examinations compared
with nonscreened patients. In a multicenter study of colon cancer in northern
California and Utah, sigmoidoscopic screening was associated with a decreased
incidence of colon cancer in both men (OR = 0.56; 95% CI, 0.44–0.77) and women
(OR = 0.53; 95% CI, 0.33–0.77) after adjusting for other risk factors for colon
cancer.[42]
A population-based mass screening program with proctoscopy for CRC in one Chinese province was associated with a reduction in incidence and mortality from rectal cancer. Mortality decreased from 4.20 (in 1974–1976) per 100,000 to 2.98 (in 1992–1996) per 100,000.[43]
In a population-based, case-control study in Germany, 39%, 77%, and 64% of proximal, distal, and total CRCs, respectively, were estimated to be preventable by colonoscopy. The estimated proportion of total CRCs preventable by sigmoidoscopy was 45% among both women and men, assuming that sigmoidoscopy reaches the junction of the descending and sigmoid colon only and that findings of distal polyps are not followed by colonoscopy. Assuming that sigmoidoscopy reaches the splenic flexure and colonoscopy is done after detection of distal polyps, estimated proportions of total CRCs preventable by sigmoidoscopy increased to 50% and 55% (73% and 91% of total CRCs preventable by primary colonoscopy) among women and men, respectively.
Based on an extensive evidence-based review, guidelines have been formulated by
representatives from a consortium of medical societies for screening and
surveillance of those at average risk and those at increased risk for
CRC because of a family history of CRC or genetic
syndromes or a personal history of adenomatous polyps, inflammatory bowel
disease, or curative-intent resection of CRC.[44] Adherence to
screening by FOBT and sigmoidoscopy is below 50% in unselected population
studies.[45]
Among research patients in a large-scale randomized clinical trial of screening, more than 85% accepted repeat sigmoidoscopy after 3 years. An uncomfortable or technically inadequate initial examination, which may be more common in women, had an adverse effect on subsequent adherence.[46,47]
An optimal frequency for CRC screening has not been rigorously established. Various organizations have recommended a 5-year interval for repeat sigmoidoscopy based on data from observational studies.[48,49] One case-control study found a negative association between sigmoidoscopy and mortality that persisted for as many as 10 years,[40] while another case-control study of endoscopy found an effect only for as many as 6 years. In contrast, other studies have examined the yield of adenomas [50] and cancers [50,51] in the distal colon 3 years after a negative sigmoidoscopy.[50] After only 3 years, potentially dangerous neoplasms were discovered; 72 advanced adenomas and six cancers were identified among 9,317 individuals examined.
Combination of FOBT and Flexible Sigmoidoscopy
In 2,885 veterans (97% male; mean age 63 years), the prevalence of advanced
adenoma at colonoscopy was 10.6%. It was estimated that combined screening
with one-time FOBT and sigmoidoscopy would detect 75.8%
(95% CI, 71.0%–80.6%) of advanced neoplasms. Examination of the rectum and
sigmoid colon during colonoscopy was defined as a surrogate for sigmoidoscopy.
This represented a small but statistically insignificant increase in rate of
detection of advanced neoplasia when compared with FS alone
(70.3%; 95% CI, 65.2%–75.4%). The latter result could be achieved assuming that
all patients with an adenoma in the distal colon undergo complete colonoscopy.
Advanced neoplasia was defined as a lesion measuring at least 10 mm in
diameter, containing 25% or more villous histology, high-grade dysplasia, or
invasive cancer.[52] One-time use of FOBT differs from
the annual or biennial application reported in those studies summarized in Table 1 3.
The Norwegian Colorectal Cancer Prevention once-only screening study randomly assigned 20,780 men and women, aged 50 to 64 years, to FS only or a combination of FS and FOBT with FlexSure OBT.[53] A positive FS was defined as a finding of any neoplasia or any polyp at least 10.0 mm. A positive FS or FOBT qualified for colonoscopy. Attendance in this study was 65%. Forty-one cases of CRC were detected (0.3% of screened individuals). Adenomas were found in 2,208 participants (17%), and 545 (4.2%) had high-risk adenomas. There was no difference in diagnosis yield between the FS only and the FS and FOBT groups regarding CRC or high-risk adenoma. There were no serious complications after FS, but there were six perforations after therapeutic colonoscopy (1:336).
Barium Enema
As part of the National Polyp Study, colonoscopic examination and barium enema
were compared in paired surveillance examinations in those who had undergone a
prior colonoscopic polypectomy.[54] The proportion of examinations in which
adenomatous polyps were detected by barium enema was related to the size of the
adenoma (P = .009); the rate was 32% for colonoscopic examinations in which the
largest adenomas detected were no larger than 5.0 mm, 53% for those in which the
largest adenomas detected were 6.0 mm to 10.0 mm, and 48% for those in which the
largest adenomas detected were larger than 10.0 mm. In patients who have undergone
colonoscopic polypectomy, colonoscopic examination is a more sensitive method
of surveillance than double-contrast barium enema.
Colonoscopy
In a colonoscopic study of 3,121 predominantly male U.S. veterans (mean age: 63
years), advanced neoplasia (defined as an adenoma that was ≥10.0 mm in
diameter, a villous adenoma, an adenoma with high-grade dysplasia, or invasive
cancer) was identified in 10.5% of the individuals.[55] Among patients with no
adenomas distal to the splenic flexure, 2.7% had advanced proximal neoplasia.
Patients with large adenomas (≥10.0 mm) or small adenomas (<10.0 mm) in the
distal colon were more likely to have advanced proximal neoplasia than were
patients with no distal adenomas (OR = 3.4; 90% CI, 1.8–6.5 and OR = 2.6; 90% CI,
1.7–4.1, respectively). One-half of those with advanced proximal neoplasia, however, had no
distal adenomas. In a study of 1,994 adults (aged 50 years or older) who
underwent colonoscopic screening as part of a program sponsored by an employer,
5.6% had advanced neoplasms.[56] Forty-six percent of those with advanced
proximal neoplasms had no distal polyps (hyperplastic or adenomatous). If
colonoscopic screening is performed only in patients with distal polyps, about
half the cases of advanced proximal neoplasia will not be detected.
A study of colonoscopy in women compared the yield of sigmoidoscopy versus colonoscopy. Among 1,463 women, cancer was found in one and advanced colonic neoplasia in 72 women or 4.9% (about one-half the prevalence compared with men). The authors focused, however, on RR (i.e., RR of missing an advanced neoplasm) as the outcome, instead of absolute risk of such neoplasms, which is substantially lower in women. In addition, the natural history of advanced neoplasia is not known, so its importance as an outcome in studies of detection is not clear.[57]
Analysis of data from a colonoscopy-based screening program in Warsaw, Poland demonstrated higher rates of advanced neoplasia in men than in women. The predominant age range of participants was 50 to 66 years. Of the 43,042 participants aged 50 to 66 years, advanced neoplasia was detected in 5.9% (5.7% among women with a family history of CRC; 4.3% among women without a family history of CRC; 12.2% among men with a family history; and 8.0% among men without a family history of CRC). Clinically significant complications requiring medical intervention were rare (0.1%) consisting of five perforations, 13 episodes of bleeding, 22 cardiovascular events, and 11 other events over the entire population of 50,148 screened persons. There were no deaths; however, the author reported that collection of 30-day complications data was not systematic (therefore, the data may not be reliable).[58]
Detection rates in colonoscopy screening vary with the rate at which the endoscopist examines the colon while withdrawing the scope. Detection rates among gastroenterologists (mean number of lesions per patient screened, 0.10 to 1.05; range of the percentage of patients with adenomas, 9.4% to 23.7%) and times to withdraw (3.1 to 16.8 minutes for procedures not including polyp removal). Examiners whose mean withdrawal time was 6 minutes or more had higher detection rates than those with mean withdrawal times of less than 6 minutes (28.3% vs. 11.8%; P < .001 for any neoplasia) and (6.4% vs. 2.6%; P < .005 for advanced neoplasia).[59] Overall detection rate of adenomas and cancer may be affected by how thoroughly endoscopists search for "flat adenomas" and "flat cancer." While the phenomenon of "flat neoplasms" has been appreciated for years in Japan, it has more recently been described in the United States. In a study in which endoscopists used high-resolution white-light endoscopes, flat or "nonpolypoid" lesions were found to account for only 11% of all superficial colon lesions, but they were about 9.8 times as likely to contain cancer (in situ neoplasia or invasive cancer) compared with "polypoid" lesions.[60] However, because the definition of flat or "nonpolypoid" was "height less than ½ the diameter," it is likely that many lesions classified as "nonpolypoid" in this study would be routinely found and described by U.S. endoscopists as "sessile." At the same time, the existence of very flat or depressed lesions (depressed lesions are very uncommon but are highly likely to contain cancer) means that endoscopists will want to pay increasing attention to this problem.[61] Flat lesions may play a role in the phenomenon of “missed cancers.”[62]
Virtual Colonoscopy (Computed Tomographic Colonography)
Virtual colonoscopy (also known as computed tomographic [CT] colonography or CT pneumocolon) refers to the examination of computer-generated images of the colon constructed from data obtained from an abdominal CT examination. These images simulate the effect of a conventional colonoscopy. Patients must take laxatives to clean the colon before the procedure, and the colon is insufflated with air (sometimes carbon dioxide) by insertion of a rectal tube just prior to radiographic examination.[63]
The performance of virtual colonoscopy depends heavily on the size of the target lesion. In a series of 300 patients who were referred for CRC screening or the evaluation of symptoms and who underwent CT colonography followed by conventional colonoscopy, investigators obtained sensitivities for CT colonography of 90% for 83 polyps measuring larger than 10.0 mm and 80% for 141 polyps measuring 5.0 to 9.9 mm. The per patient sensitivity for the 10.0 mm lesion size was 94% (64 of 68), and it was 66.9% (95 of 142) for adenomas smaller than 5.0 mm. CT colonography led to false identification of 45 polyps ranging in size from 3.0 mm to 17.0 mm in patients who had normal colonoscopic results. Overall performance characteristics for CT colonography were similar when comparing results for the 96 individuals without symptoms to results for the 204 symptomatic individuals.[64]
In a separate series of 201 patients who had symptoms suggestive of colorectal disease or who were undergoing surveillance because of prior colorectal neoplasia, investigators found that CT colonography detected all 13 CRCs identified in 13 patients on (endoscopic) colonoscopy, but only 20 (7 > 10.0 mm) of the 118 (14 > 10.0 mm) polyps in 63 patients. Sensitivity for detection of invasive carcinoma and/or polyps 10.0 mm or larger in diameter was 73% (95% CI, 56%–90%), and the specificity was 94% (95% CI, 91%–98%).[65]
One thousand two hundred thirty-three asymptomatic adults underwent complete virtual and optical colonoscopic examinations (728 men and 505 women; mean age 57.8 years) at several U.S. institutions employing an identical state-of-the-art protocol between May 2002 and June 2003. Extraordinary care was given to bowel preparation, and stool tagging was employed to minimize artifacts. High-speed, thin-section, supine-position and prone-position, single breath-hold scans were reconstructed in both two dimensions (2-D) and three dimensions (3-D), but the 3-D data were relied upon for image interpretation, using commercially available software.
Polyps were measured with electronic calipers and recorded according to colonic segment. Extracolonic findings were also recorded. CT colonographic studies were prospectively interpreted by one of six board-certified radiologists, each previously trained on a minimum of 25 CT colonographic studies, immediately before optical colonoscopic examination. Optical colonoscopies were performed by 17 experienced gastroenterologists or colorectal surgeons who were initially unaware of the CT findings. Polyps were photographed and measured with a calibrated linear probe.
CT results were unblinded segment by segment to the colonoscopists to allow them to re-evaluate their findings in light of the additional CT information, and thereby create a reference standard against which both CT colonography and optical colonoscopy findings could be compared. Performance characteristics for CT (and optical) colonoscopy were calculated for adenomatous polyps. Sensitivity of CT colonography increased from 88.7% (149/168), for adenomas at least 6.0 mm, to 93.8% (45/48), for adenomas at least 10.0 mm, with respective specificities of 79.6% and 96.0%. (Sensitivities for optical colonoscopy in the absence of CT information were, respectively, by size 92.3% and 87.5%.)
Most of the polyps found on CT colonography, but not on the initial optical colonoscopy, were situated behind a colonic fold, that is “recognized as a relative blind spot” for optical colonoscopy. Interobserver agreement for independent double readings of CT colonography studies, segment by segment, was good, 99.6% for polyps at least 10.0 mm and 97.6% for polyps at least 6.0 mm. Only two cancers were detected in this asymptomatic population, one by optical colonoscopy and both by CT colonography. Fifty-six patients (4.5%) had extracolonic findings considered to be potentially clinically important and needing medical workup.[66]
Another study reported very different results. This study was a prospective evaluation of CT colonography among 600 participants who were seen at nine large medical centers. The participants were referred for routine clinically indicated colonoscopy, and CT colonography was performed immediately prior to the colonoscopy using multidetector scanning. The accuracy of CT colonography was substantially lower than previously reported; 39% of lesions less than 6 mm and 55% of lesions less than 1 cm were detected and six out of eight cancers were detected using CT colonography. Additionally, the accuracy of CT colonography varied substantially among centers and did not improve over time. Of note, some of the imaging techniques used in previously published reports were not used in this study, and that might explain, in part, the low sensitivity of the test in this report. The authors conclude, however, that techniques and training need to be improved before widespread use because most clinically significant polyps were missed.[67]
A study has assessed how well virtual colonoscopy can detect colorectal polyps without a laxative prep. The question is of great importance for implementation because the laxative prep required by both conventional colonoscopy, and virtual colonoscopy is considered a great disadvantage by patients. By tagging feces with iodinated contrast material ingested during several days prior to the procedure, investigators were able to detect lesions larger than 8 mm with 95% sensitivity and 92% specificity.[68] The particular tagging material used in this study caused about 10% of patients to become nauseated, however; other materials are being assessed. While a number of hurdles remain to be overcome before virtual colonoscopy becomes popular and widely used,[69] this study provides important preliminary data suggesting that the problem of laxative preparation might be successfully addressed.
Extracolonic abnormalities are common in CT colonography. Fifteen percent of patients in an Australian series of 100 patients, referred for colonography because of symptoms or family history, were found to have extracolonic findings, 11 needing further medical workups for renal, splenic, uterine, liver, and gallbladder abnormalities.[70] In another study, 59% of 111 symptomatic patients referred for clinical colonoscopy in a Swedish hospital between June 1998 and September 1999 were found to have moderate or major extracolonic conditions on CT colonography. CT colonography was performed immediately prior to colonoscopy and these findings required further evaluation. It is unstated to what extent the follow-up of these incidental findings benefited patients.[71]
Sixty-nine percent of 681 asymptomatic patients in Minnesota had extracolonic findings, of which 10% were considered to be “highly important” by the investigators, requiring further medical workup. Suspected abnormalities involved kidney (34), chest (22), liver (8), ovary (6), renal or splenic arteries (4), retroperitoneum (3), and pancreas (1);[72] however, the extent to which these findings will contribute to benefits or harms is uncertain.
Technical improvements involving both the interpretation methodology, such as 3-D imaging, and bowel preparation are under study in many centers. While specificity for detection of polyps is homogeneously high in many studies, sensitivity can vary widely. These variations are attributable to a number of factors including characteristics of the CT scanner and detector, width of collimation, mode of imaging (2-D vs. 3-D and/or "fly-through"), as well as variability in expertise of radiologists.[73]
Digital Rectal Examination
A case-control study reported that routine digital rectal examination was not
associated with any statistically significant reduction in mortality from
distal rectal cancer.[74]
Detection of DNA Mutations in the Stool
The molecular genetic changes that are associated with the development of
colorectal adenomas and carcinoma have been well characterized.[75] Advanced
techniques have been developed to detect several of these gene mutations that
have been shed into the stool.[76-79] Stool DNA testing was recently assessed in a prospective study of asymptomatic persons who received colonoscopy, three-card FOBT (Hemoccult II), and stool DNA testing based on a panel of markers assessing 21 mutations. Conducted in a blinded way with prestated hypotheses and analyses, the study found that among 4,404 patients, the DNA panel had a sensitivity for CRC of 51.6% (for all stages of CRC) versus 12.9% for Hemoccult II, while the false-positive rates were 5.6% and 4.8%, respectively. On this basis, the approach looks promising but would be improved, if possible, by increased sensitivity (perhaps by increasing the number of DNA markers) and by reduced cost.[80,81]
References
-
Kewenter J, Björk S, Haglind E, et al.: Screening and rescreening for colorectal cancer. A controlled trial of fecal occult blood testing in 27,700 subjects. Cancer 62 (3): 645-51, 1988.
[PUBMED Abstract]
-
Hardcastle JD, Thomas WM, Chamberlain J, et al.: Randomised, controlled trial of faecal occult blood screening for colorectal cancer. Results for first 107,349 subjects. Lancet 1 (8648): 1160-4, 1989.
[PUBMED Abstract]
-
Kronborg O, Fenger C, Søndergaard O, et al.: Initial mass screening for colorectal cancer with fecal occult blood test. A prospective randomized study at Funen in Denmark. Scand J Gastroenterol 22 (6): 677-86, 1987.
[PUBMED Abstract]
-
Kronborg O, Fenger C, Olsen J, et al.: Repeated screening for colorectal cancer with fecal occult blood test. A prospective randomized study at Funen, Denmark. Scand J Gastroenterol 24 (5): 599-606, 1989.
[PUBMED Abstract]
-
Winawer SJ, Flehinger BJ, Schottenfeld D, et al.: Screening for colorectal cancer with fecal occult blood testing and sigmoidoscopy. J Natl Cancer Inst 85 (16): 1311-8, 1993.
[PUBMED Abstract]
-
Mandel JS, Bond JH, Church TR, et al.: Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota Colon Cancer Control Study. N Engl J Med 328 (19): 1365-71, 1993.
[PUBMED Abstract]
-
Mandel JS, Church TR, Ederer F, et al.: Colorectal cancer mortality: effectiveness of biennial screening for fecal occult blood. J Natl Cancer Inst 91 (5): 434-7, 1999.
[PUBMED Abstract]
-
Lang CA, Ransohoff DF: Fecal occult blood screening for colorectal cancer. Is mortality reduced by chance selection for screening colonoscopy? JAMA 271 (13): 1011-3, 1994.
[PUBMED Abstract]
-
Ederer F, Church TR, Mandel JS: Fecal occult blood screening in the Minnesota study: role of chance detection of lesions. J Natl Cancer Inst 89 (19): 1423-8, 1997.
[PUBMED Abstract]
-
Mandel JS, Church TR, Bond JH, et al.: The effect of fecal occult-blood screening on the incidence of colorectal cancer. N Engl J Med 343 (22): 1603-7, 2000.
[PUBMED Abstract]
-
Hardcastle JD, Chamberlain JO, Robinson MH, et al.: Randomised controlled trial of faecal-occult-blood screening for colorectal cancer. Lancet 348 (9040): 1472-7, 1996.
[PUBMED Abstract]
-
Robinson MH, Hardcastle JD, Moss SM, et al.: The risks of screening: data from the Nottingham randomised controlled trial of faecal occult blood screening for colorectal cancer. Gut 45 (4): 588-92, 1999.
[PUBMED Abstract]
-
Scholefield JH, Moss S, Sufi F, et al.: Effect of faecal occult blood screening on mortality from colorectal cancer: results from a randomised controlled trial. Gut 50 (6): 840-4, 2002.
[PUBMED Abstract]
-
Kronborg O, Fenger C, Olsen J, et al.: Randomised study of screening for colorectal cancer with faecal-occult-blood test. Lancet 348 (9040): 1467-71, 1996.
[PUBMED Abstract]
-
Jørgensen OD, Kronborg O, Fenger C: A randomised study of screening for colorectal cancer using faecal occult blood testing: results after 13 years and seven biennial screening rounds. Gut 50 (1): 29-32, 2002.
[PUBMED Abstract]
-
Kronborg O, Jørgensen OD, Fenger C, et al.: Randomized study of biennial screening with a faecal occult blood test: results after nine screening rounds. Scand J Gastroenterol 39 (9): 846-51, 2004.
[PUBMED Abstract]
-
Moayyedi P, Achkar E: Does fecal occult blood testing really reduce mortality? A reanalysis of systematic review data. Am J Gastroenterol 101 (2): 380-4, 2006.
[PUBMED Abstract]
-
Gyrd-Hansen D, Søgaard J, Kronborg O: Colorectal cancer screening: efficiency and effectiveness. Health Econ 7 (1): 9-20, 1998.
[PUBMED Abstract]
-
Loeve F, Boer R, van Oortmarssen GJ, et al.: The MISCAN-COLON simulation model for the evaluation of colorectal cancer screening. Comput Biomed Res 32 (1): 13-33, 1999.
[PUBMED Abstract]
-
Wagner JL, Tunis S, Brown M, et al.: Cost-effectiveness of colorectal cancer screening in average-risk adults. In: Young GP, Rozen P, Levin B, eds.: Prevention and Early Detection of Colorectal Cancer. London, England: WB Saunders, 1996, pp 321-356.
-
Whynes DK, Neilson AR, Walker AR, et al.: Faecal occult blood screening for colorectal cancer: is it cost-effective? Health Econ 7 (1): 21-9, 1998.
[PUBMED Abstract]
-
Suggested technique for fecal occult blood testing and interpretation in colorectal cancer screening. American College of Physicians. Ann Intern Med 126 (10): 808-10, 1997.
[PUBMED Abstract]
-
Ransohoff DF, Lang CA: Screening for colorectal cancer with the fecal occult blood test: a background paper. American College of Physicians. Ann Intern Med 126 (10): 811-22, 1997.
[PUBMED Abstract]
-
Hewitson P, Glasziou P, Irwig L, et al.: Screening for colorectal cancer using the faecal occult blood test, Hemoccult. Cochrane Database Syst Rev (1): CD001216, 2007.
[PUBMED Abstract]
-
Malila N, Hakama M, Pukkala E: A 25-year follow-up of a population screened with faecal occult blood test in Finland. Acta Oncol 46 (8): 1103-6, 2007.
[PUBMED Abstract]
-
Eddy DM: Screening for colorectal cancer. Ann Intern Med 113 (5): 373-84, 1990.
[PUBMED Abstract]
-
Allison JE, Feldman R, Tekawa IS: Hemoccult screening in detecting colorectal neoplasm: sensitivity, specificity, and predictive value. Long-term follow-up in a large group practice setting. Ann Intern Med 112 (5): 328-33, 1990.
[PUBMED Abstract]
-
Levi Z, Rozen P, Hazazi R, et al.: A quantitative immunochemical fecal occult blood test for colorectal neoplasia. Ann Intern Med 146 (4): 244-55, 2007.
[PUBMED Abstract]
-
Morikawa T, Kato J, Yamaji Y, et al.: A comparison of the immunochemical fecal occult blood test and total colonoscopy in the asymptomatic population. Gastroenterology 129 (2): 422-8, 2005.
[PUBMED Abstract]
-
Burch JA, Soares-Weiser K, St John DJ, et al.: Diagnostic accuracy of faecal occult blood tests used in screening for colorectal cancer: a systematic review. J Med Screen 14 (3): 132-7, 2007.
[PUBMED Abstract]
-
Fath RB, Winawer SJ: Endoscopic screening by flexible fiberoptic sigmoidoscopy. Front Gastrointest Res 10: 102-111, 1986.
-
Read TE, Read JD, Butterly LF: Importance of adenomas 5 mm or less in diameter that are detected by sigmoidoscopy. N Engl J Med 336 (1): 8-12, 1997.
[PUBMED Abstract]
-
Wallace MB, Kemp JA, Trnka YM, et al.: Is colonoscopy indicated for small adenomas found by screening flexible sigmoidoscopy? Ann Intern Med 129 (4): 273-8, 1998.
[PUBMED Abstract]
-
Levin TR, Palitz A, Grossman S, et al.: Predicting advanced proximal colonic neoplasia with screening sigmoidoscopy. JAMA 281 (17): 1611-7, 1999.
[PUBMED Abstract]
-
Winawer SJ, Zauber AG, Ho MN, et al.: Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup. N Engl J Med 329 (27): 1977-81, 1993.
[PUBMED Abstract]
-
Rembacken BJ, Fujii T, Cairns A, et al.: Flat and depressed colonic neoplasms: a prospective study of 1000 colonoscopies in the UK. Lancet 355 (9211): 1211-4, 2000.
[PUBMED Abstract]
-
Hertz RE, Deddish MR, Day E: Value of periodic examinations in detecting cancer of the rectum and colon. Postgrad Med 27: 290-294, 1960.
-
Gilbertsen VA: Proctosigmoidoscopy and polypectomy in reducing the incidence of rectal cancer. Cancer 34 (3): suppl:936-9, 1974.
[PUBMED Abstract]
-
Friedman GD, Collen MF, Fireman BH: Multiphasic Health Checkup Evaluation: a 16-year follow-up. J Chronic Dis 39 (6): 453-63, 1986.
[PUBMED Abstract]
-
Selby JV, Friedman GD, Quesenberry CP Jr, et al.: A case-control study of screening sigmoidoscopy and mortality from colorectal cancer. N Engl J Med 326 (10): 653-7, 1992.
[PUBMED Abstract]
-
Newcomb PA, Norfleet RG, Storer BE, et al.: Screening sigmoidoscopy and colorectal cancer mortality. J Natl Cancer Inst 84 (20): 1572-5, 1992.
[PUBMED Abstract]
-
Slattery ML, Edwards SL, Ma KN, et al.: Colon cancer screening, lifestyle, and risk of colon cancer. Cancer Causes Control 11 (6): 555-63, 2000.
[PUBMED Abstract]
-
Zheng S, Liu XY, Ding KF, et al.: Reduction of the incidence and mortality of rectal cancer by polypectomy: a prospective cohort study in Haining County. World J Gastroenterol 8 (3): 488-92, 2002.
[PUBMED Abstract]
-
Winawer SJ, Fletcher RH, Miller L, et al.: Colorectal cancer screening: clinical guidelines and rationale. Gastroenterology 112 (2): 594-642, 1997.
[PUBMED Abstract]
-
Vernon SW: Participation in colorectal cancer screening: a review. J Natl Cancer Inst 89 (19): 1406-22, 1997.
[PUBMED Abstract]
-
Weissfeld JL, Ling BS, Schoen RE, et al.: Adherence to repeat screening flexible sigmoidoscopy in the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial. Cancer 94 (10): 2569-76, 2002.
[PUBMED Abstract]
-
Weissfeld JL, Schoen RE, Pinsky PF, et al.: Flexible sigmoidoscopy in the PLCO cancer screening trial: results from the baseline screening examination of a randomized trial. J Natl Cancer Inst 97 (13): 989-97, 2005.
[PUBMED Abstract]
-
Winawer S, Fletcher R, Rex D, et al.: Colorectal cancer screening and surveillance: clinical guidelines and rationale-Update based on new evidence. Gastroenterology 124 (2): 544-60, 2003.
[PUBMED Abstract]
-
Smith RA, von Eschenbach AC, Wender R, et al.: American Cancer Society guidelines for the early detection of cancer: update of early detection guidelines for prostate, colorectal, and endometrial cancers. Also: update 2001--testing for early lung cancer detection. CA Cancer J Clin 51 (1): 38-75; quiz 77-80, 2001 Jan-Feb.
[PUBMED Abstract]
-
Schoen RE, Pinsky PF, Weissfeld JL, et al.: Results of repeat sigmoidoscopy 3 years after a negative examination. JAMA 290 (1): 41-8, 2003.
[PUBMED Abstract]
-
Doria-Rose VP, Levin TR, Selby JV, et al.: The incidence of colorectal cancer following a negative screening sigmoidoscopy: implications for screening interval. Gastroenterology 127 (3): 714-22, 2004.
[PUBMED Abstract]
-
Lieberman DA, Weiss DG; Veterans Affairs Cooperative Study Group 380.: One-time screening for colorectal cancer with combined fecal occult-blood testing and examination of the distal colon. N Engl J Med 345 (8): 555-60, 2001.
[PUBMED Abstract]
-
Gondal G, Grotmol T, Hofstad B, et al.: The Norwegian Colorectal Cancer Prevention (NORCCAP) screening study: baseline findings and implementations for clinical work-up in age groups 50-64 years. Scand J Gastroenterol 38 (6): 635-42, 2003.
[PUBMED Abstract]
-
Winawer SJ, Stewart ET, Zauber AG, et al.: A comparison of colonoscopy and double-contrast barium enema for surveillance after polypectomy. National Polyp Study Work Group. N Engl J Med 342 (24): 1766-72, 2000.
[PUBMED Abstract]
-
Lieberman DA, Weiss DG, Bond JH, et al.: Use of colonoscopy to screen asymptomatic adults for colorectal cancer. Veterans Affairs Cooperative Study Group 380. N Engl J Med 343 (3): 162-8, 2000.
[PUBMED Abstract]
-
Imperiale TF, Wagner DR, Lin CY, et al.: Risk of advanced proximal neoplasms in asymptomatic adults according to the distal colorectal findings. N Engl J Med 343 (3): 169-74, 2000.
[PUBMED Abstract]
-
Schoenfeld P, Cash B, Flood A, et al.: Colonoscopic screening of average-risk women for colorectal neoplasia. N Engl J Med 352 (20): 2061-8, 2005.
[PUBMED Abstract]
-
Regula J, Rupinski M, Kraszewska E, et al.: Colonoscopy in colorectal-cancer screening for detection of advanced neoplasia. N Engl J Med 355 (18): 1863-72, 2006.
[PUBMED Abstract]
-
Barclay RL, Vicari JJ, Doughty AS, et al.: Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 355 (24): 2533-41, 2006.
[PUBMED Abstract]
-
Soetikno RM, Kaltenbach T, Rouse RV, et al.: Prevalence of nonpolypoid (flat and depressed) colorectal neoplasms in asymptomatic and symptomatic adults. JAMA 299 (9): 1027-35, 2008.
[PUBMED Abstract]
-
Lieberman D: Nonpolypoid colorectal neoplasia in the United States: the parachute is open. JAMA 299 (9): 1068-9, 2008.
[PUBMED Abstract]
-
Robertson DJ, Greenberg ER, Beach M, et al.: Colorectal cancer in patients under close colonoscopic surveillance. Gastroenterology 129 (1): 34-41, 2005.
[PUBMED Abstract]
-
Ferrucci JT: Colon cancer screening with virtual colonoscopy: promise, polyps, politics. AJR Am J Roentgenol 177 (5): 975-88, 2001.
[PUBMED Abstract]
-
Yee J, Akerkar GA, Hung RK, et al.: Colorectal neoplasia: performance characteristics of CT colonography for detection in 300 patients. Radiology 219 (3): 685-92, 2001.
[PUBMED Abstract]
-
Miao YM, Amin Z, Healy J, et al.: A prospective single centre study comparing computed tomography pneumocolon against colonoscopy in the detection of colorectal neoplasms. Gut 47 (6): 832-7, 2000.
[PUBMED Abstract]
-
Pickhardt PJ, Choi JR, Hwang I, et al.: Computed tomographic virtual colonoscopy to screen for colorectal neoplasia in asymptomatic adults. N Engl J Med 349 (23): 2191-200, 2003.
[PUBMED Abstract]
-
Cotton PB, Durkalski VL, Pineau BC, et al.: Computed tomographic colonography (virtual colonoscopy): a multicenter comparison with standard colonoscopy for detection of colorectal neoplasia. JAMA 291 (14): 1713-9, 2004.
[PUBMED Abstract]
-
Iannaccone R, Laghi A, Catalano C, et al.: Computed tomographic colonography without cathartic preparation for the detection of colorectal polyps. Gastroenterology 127 (5): 1300-11, 2004.
[PUBMED Abstract]
-
McFarland EG, Zalis ME: CT colonography: progress toward colorectal evaluation without catharsis. Gastroenterology 127 (5): 1623-6, 2004.
[PUBMED Abstract]
-
Edwards JT, Wood CJ, Mendelson RM, et al.: Extracolonic findings at virtual colonoscopy: implications for screening programs. Am J Gastroenterol 96 (10): 3009-12, 2001.
[PUBMED Abstract]
-
Hellström M, Svensson MH, Lasson A: Extracolonic and incidental findings on CT colonography (virtual colonoscopy). AJR Am J Roentgenol 182 (3): 631-8, 2004.
[PUBMED Abstract]
-
Gluecker TM, Johnson CD, Wilson LA, et al.: Extracolonic findings at CT colonography: evaluation of prevalence and cost in a screening population. Gastroenterology 124 (4): 911-6, 2003.
[PUBMED Abstract]
-
Mulhall BP, Veerappan GR, Jackson JL: Meta-analysis: computed tomographic colonography. Ann Intern Med 142 (8): 635-50, 2005.
[PUBMED Abstract]
-
Herrinton LJ, Selby JV, Friedman GD, et al.: Case-control study of digital-rectal screening in relation to mortality from cancer of the distal rectum. Am J Epidemiol 142 (9): 961-4, 1995.
[PUBMED Abstract]
-
Kinzler KW, Vogelstein B: Lessons from hereditary colorectal cancer. Cell 87 (2): 159-70, 1996.
[PUBMED Abstract]
-
Dong SM, Traverso G, Johnson C, et al.: Detecting colorectal cancer in stool with the use of multiple genetic targets. J Natl Cancer Inst 93 (11): 858-65, 2001.
[PUBMED Abstract]
-
Traverso G, Shuber A, Levin B, et al.: Detection of APC mutations in fecal DNA from patients with colorectal tumors. N Engl J Med 346 (5): 311-20, 2002.
[PUBMED Abstract]
-
Traverso G, Shuber A, Olsson L, et al.: Detection of proximal colorectal cancers through analysis of faecal DNA. Lancet 359 (9304): 403-4, 2002.
[PUBMED Abstract]
-
Ahlquist DA, Skoletsky JE, Boynton KA, et al.: Colorectal cancer screening by detection of altered human DNA in stool: feasibility of a multitarget assay panel. Gastroenterology 119 (5): 1219-27, 2000.
[PUBMED Abstract]
-
Imperiale TF, Ransohoff DF, Itzkowitz SH, et al.: Fecal DNA versus fecal occult blood for colorectal-cancer screening in an average-risk population. N Engl J Med 351 (26): 2704-14, 2004.
[PUBMED Abstract]
-
Woolf SH: A smarter strategy? Reflections on fecal DNA screening for colorectal cancer. N Engl J Med 351 (26): 2755-8, 2004.
[PUBMED Abstract]
|