Title: Screening for colorectal cancer
1Screening for colorectal cancer
- Nigel Williams
- University Hospitals Coventry and Warwickshire
2Philosophy of screening
- The early detection of cancer in a
population setting makes the following
assumptions -
- The Screening test is reliable and indicates
the presence of cancer -
- There are few false positive and false
negatives - The test is easy to apply and interpret
3Philosophy of screening
- The early detection of cancer in a
population setting makes the following
assumptions -
- The Screening test is inexpensive
- The test does not incur significant hazard to
people screened - That early diagnosis will significantly alter
the natural history of the disease
4Philosophy of screening
-
- Lead time bias
- Although early treatment of a cancer may result
in an apparently longer overall survival.there
may be no overall change in the natural history
of the disease
5CRC screening
- Colorectal cancer is ideally suited to
screening - It is common (28-30 000 new cases/yr)
- There is a clearly identified premalignant
lesion - Treatment of the premalignant lesion reduces
the risk of cancer - Early detection of CRC improves overall
survival - The cost effectiveness of screening compares
favourably with other screening strategies (eg
breast, cervical) -
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7CRC screening- the data
Mandel JS Minnesota Hardcastle Nottingham Kronberg
Odense (Denmark) All were large scale RCTs in a
population setting
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9CRC screening- the data
All three RCTs have demonstrated a reduction in
the risk of dying from colorectal cancer. A
meta-analysis of trials using Haemoccult reported
a 16 reduction in colorectal cancer mortality
10CRC screening- present guidelines
11CRC screening- present guidelines
12CRC screening- guidelines
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14CRC screening- what they say
There is no longer any doubt that screening is an
effective method of reducing colorectal cancer
incidence and mortality rates Atkin WS,
Northover JMA Gut 2002
15CRC screening- what they say
The persistent reduction in mortality from CRC in
a biennial screening program with Haemoccult-II
and a reduction in relative risk to less than
0.70.support attempts to introduce larger scale
population screening programmes. Jorgensen OD et
al Gut 2002 50 29-32
16CRC screening- what they say
There is no longer any doubt that screening is an
effective method of reducing colorectal cancer
incidence and mortality rates. The US
Preventative Services Task Force recently
reviewed the evidence and gave a grade A
recommendation that all men and women should be
screened for CRC Smith RA et al CA Cancer J
Clin 2004 54 41-52
17CRC screening- how?
FOBT - to rehydrate or not - how often FOBT
FS Colonoscopy Virtual colonoscopy Immunological G
enetic testing of stool DNA
18CRC screening- the reality
The UK Colorectal Cancer Screening Pilot was
established to determine the feasibility of
screening for CRC in the UK population using FOBT
and colonoscopy. The English site was based in
Warwickshire and in Scotland, the population of
Dundee were selected.
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20CRC screening- the reality
Funding was for all administration and setting
up In Warwickshire 4 extra colonoscopy lists
were required and were undertaken at consultant
level. All participants had attended a
masterclass with C B Williams 4-5
colonoscopies per list
21CRC screening- the reality
FOBT kits were posted to 187 777 people The
response rate was approximately 60. The FOB
positivity rate was approximately 1.5 yielding
1700 colonoscopies over the 2 year period
22CRC screening- the reality
A small number of people declined, were excluded
for medical reasons or had their colonoscopy
performed privately If the caecum was not
intubated a DCBE was performed the same day
23CRC screening- the reality
Of those patients undergoing colonoscopy,
approximately 60 were normal, 30 had polyps and
10 had a cancer. Generally, Dukes A and B
were overrepresented compared to a symptomatic
population. It is too early for mortality and
long-term survival data to be available
24CRC screening- the debate
FOS or colonoscopy Manpower issues When to start
screening What intervals How can we reduce the
risk of polypectomy Genetic stratification of
risk