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Colorectal cancer is a disease ideal for screening: it is common;
prognosis is poor if it is detected late but excellent if it is treated
early; and there is a premalignant phase (the adenoma) which has a
relatively long dwell time during which it can be detected and treated
relatively safely. In addition, higher-than-average-risk groups
can be identified and targeted. It has been recommended that a
colorectal cancer screening program be established in Australia,
but, because of uncertainties about the program's feasibility, that
this be implemented through a series of pilot studies.1 Nonetheless,
for asymptomatic individuals aged over 50 years without a family
history of colorectal cancer, the National Health and Medical
Research Council favours screening by annual faecal occult blood
testing (FOBT), complemented by flexible sigmoidoscopy every five
years.2 The problem is that all current screening tools are imperfect. FOBT is
most widely advocated as the only test shown to reduce mortality from
colorectal cancer (by 15%-33%) when used for mass population
screening.1 It is also cheap, safe and can
be administered by the general practitioner. Accuracy depends on the
type of FOBT used and the frequency of testing, but, on an individual
basis, FOBT misses between 21% and 63% of cancers and most adenomas,
and has a false-positive rate of 2%-13%.3
Flexible sigmoidoscopy is under trial both in Australia and overseas
as a tool for population screening. The rationale is that most
neoplasms occur within reach of the flexible sigmoidoscope, and that
distal adenomas may be predictors of proximal lesions. In this issue
of the Journal, Nicholson and colleagues4 show, as
have others,5 that, among screened
subjects with adenomas, 25% have proximal adenomas only (defined by
Nicholson et al as proximal to the splenic flexure). These are beyond
the reach of flexible sigmoidoscopy. This study illustrates one of
the problems of flexible sigmoidoscopy screening -- accuracy for
cancer and polyp detection. However, other important issues must be
considered in assessing a screening test, such as acceptability,
compliance, availability, safety and cost. Indeed, in the
Australian context, initial participation rates in flexible
sigmoidoscopy screening have been disappointing (12%),6 although recent
data indicate that these rates have increased to around 40%
(Associate Professor John Olynyk, Department of Gastroenterology,
Fremantle Hospital, Fremantle, WA, personal communication).
The findings of Nicholson and colleagues support the need for imaging
the whole colon in colorectal neoplasm screening. Methods advocated
for this include double-contrast barium enema and colonoscopy. Both
have their supporters. However, data on use of these methods for
population screening of average-risk individuals are limited, and
both have drawbacks that make them unlikely to be widely accepted for
mass screening. Setting aside considerations of compliance,
double-contrast barium enema is probably not sufficiently accurate
without concomitant flexible sigmoidoscopy (which would increase
costs and almost certainly decrease compliance), and imposes a
significant radiation dose. Total colonoscopy has the advantages of
accuracy and ability to combine screening with therapy
(polypectomy) but carries a small but significant risk.7 A certain level
of competence is required to achieve adequate rates of caecal
intubation, and, although it is difficult to determine exact
completion rates, outside specialist centres they may be only
80%-90%8,9 or less. Taking into
account the need for sedation, consequent bed fees and cost of time off
work, colonoscopy is relatively expensive.
A recent contender for screening is virtual colonoscopy (computed
tomography [CT] colography). After bowel preparation, the colon is
insufflated with air or carbon dioxide, and a spiral CT scan
performed, preferably in supine and prone positions. Because of the
volumetric nature of data acquisition, sagittal and coronal
reformatted images can be viewed, as well as the source axial images,
and endoluminal images can be reconstructed, simulating an
endoscopic view. Navigation using these images can be achieved by
manual manoeuvres or "fly-through" techniques that automatically
centre on the bowel lumen. While not yet as accurate as colonoscopy for
polyp detection, virtual colonoscopy is likely to become
significantly more accurate with expected developments in hardware
and software. Currently, virtual colonoscopy is more accurate than
FOBT and can probably compete with flexible sigmoidoscopy with
regard to larger polyps. A study from Boston has reported
sensitivities of 91%, 82% and 55% for polyps of diameter 10 mm or more,
6-9 mm, and 5 mm or less, respectively.10
Virtual colonoscopy also has several potential advantages as a
screening tool: it is minimally invasive and quick for the patient
(the scan takes only a few minutes); no sedation is required; and
initial studies have shown that it is highly acceptable to
patients.11 Its "high-tech", virtual
reality profile makes it potentially attractive to the lay public.
While using ionising radiation, dosages are considerably less than
for double-contrast barium enema when low-dosage protocols are
used. Using the current scanning protocol in our institution, total
effective radiation dose has been calculated to be less than 5 mSv,
even when supine and prone scans are performed (compared with about 8
mSv for conventional double-contrast barium enema). In addition,
early studies hold out the possibility that magnetic-resonance (MR)
virtual colonoscopy may eventually supersede CT virtual
colonoscopy, eliminating ionising radiation.12 Lastly, there
is the potential to detect incidental extracolonic disease, such as
asymptomatic aortic aneurysms and renal carcinoma.
Problems currently limiting the application of virtual colonoscopy
as a screening tool include its lack of sensitivity for small polyps,
particularly those 5 mm or less in diameter.10 Does this matter in the
context of a screening program? Probably not: the chances of a 5 mm
lesion being malignant are negligible; if screening takes place
every five years the dwell time for such a small lesion allows an
enlarging lesion to be picked up on subsequent examinations. A
further limitation is the need for bowel preparation, which is likely
to be a significant factor in reducing participation rates. However,
the use of faecal tagging to allow software to differentiate faeces
and polyps may eventually minimise, or even eliminate, the need for
bowel preparation.
In addition, other factors, such as availability, operator
experience and cost, need to be evaluated in assessing the potential
role of virtual colonoscopy as a screening tool for colorectal
cancer. Much of the present cost is related to the time required for
image processing and reading of the images by the radiologist, which
is as long as 30-45 minutes with current commercially available
technology. However, this time will inevitably be reduced
significantly by further technological advances, such as faster
computer processing and automated polyp detection software.
Finally, it would be preferable that images are read promptly so that
individuals with abnormalities have the opportunity of proceeding
to same-day colonoscopy to avoid the need for a second bowel
preparation.
So, is virtual colonoscopy a viable option as a screening tool for
colorectal cancer in the average-risk individual? There is little
doubt that, in its current state of development, it is not ready for
widespread use. In addition to the limitations already discussed,
the excellent sensitivity data reported by some centres10,13 have not
been widely replicated.14 Equally, there is a high
probability that, at its rate of evolution, in the not-too-distant
future CT (or MR) virtual colonoscopy will become an accepted (or even
the accepted) modality for colorectal cancer screening. In
the meantime, while waiting for the technology to catch up,
feasibility studies of virtual colonoscopy are needed to examine
issues such as participation rates, factors affecting recruitment
into screening programs, acceptability and cost.
Richard M Mendelson Radiologist
Geoffrey M Forbes Gastroenterologist, and Clinical Senior Lecturer University of
Western Australia, Royal Perth Hospital, WA
Disclosure statement: The authors are active in clinical
research into virtual colonoscopy and are planning a feasibility
study of the technique in colorectal cancer screening.
- Australian Health Technology Advisory Committee. Colorectal
cancer screening. Canberra: AGPS, 1997.
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National Health and Medical Research Council. Guidelines for the
prevention, early detection and management of colorectal cancer.
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Allison JE, Tekawa IS, Ransom LJ, Adrain AL. A comparison of fecal
occult blood tests for colorectal-cancer screening. N Engl J
Med 1996; 334: 155-159.
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Nicholson FB, Korman MG, Stern AI, Hansky J. Distribution of
colorectal adenomas: implications for bowel cancer screening.
Med J Aust 2000; 172: 428-430.
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Kadakia SC, Wrobleski CS, Kadakia AS, Meier NJ. Prevalence of
proximal colonic polyps in average-risk asymptomatic patients with
negative fecal occult blood tests and flexible sigmoidoscopy.
Gastrointest Endosc 1996; 44: 112-117.
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Olynyk JK, Aquilia S, Fletcher DR, Dickinson JA. Flexible
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Waye J, Kahn O, Auerbach M. Complications of colonoscopy and
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Thiis-Evensen E, Hoff GS, Sauar J, et al. Flexible sigmoidoscopy or
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Freeman B, Engel JJ, Fine MS, DiVita DP. Colonoscopy to the cecum:
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Fenlon HM, Nunes DP, Schroy P, et al. A comparison of virtual and
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Forbes GM, Mendelson RM. Patient acceptance of virtual
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Debatin JF, Luboldt W, Bauerfeind P. Virtual colonoscopy in 1999:
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Endoscopy 1999; 31: 174-179.
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Kay CL, Kulling D, Hawes RH, et al. Virtual endoscopy -- comparison
with colonoscopy in the detection of space-occupying lesions of the
colon. Endoscopy 2000; 32: 226-232.
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Rex DK, Vining D, Kopecky KK. An initial experience with screening
for colon polyps using spiral CT with and without CT colography
(virtual colonoscopy). Gastrointest Endosc 1999; 50:
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