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ANDREW LATCHFORD
BSc, MBBS, MD, FRCP
CONSULTANT
GASTROENTEROLOGIST
www.bowelcancerwest.org.uk
BACKGROUND COLORECTAL
CANCER
Interaction
between genotype and
the environment
The UK lifetime risk of CRC is ≈5%
Many people by chance alone have at
least one affected relative
number of affected relatives,
risk
of developing CRC
www.bowelcancerwest.org.uk
GENETIC RISK
Spectrum
of risk
High-risk, overwhelming contribution
of genotype
– ≤5% CRC, at risk of ‘inherited bowel
cancer’
Low-
and moderate-risk, genotype
contributes to risk, role in ≈30%
www.bowelcancerwest.org.uk
ASSESSMENT OF RISK
Accurate
family history
– site and age at diagnosis of ALL cancers in
family members,
– presence of colorectal adenomas/other polyps
The
family history has limitations
– small families
– incorrect information, early death of
individuals before they develop cancers.
www.bowelcancerwest.org.uk
ASSESSMENT OF RISK
A
full personal history
– symptoms
– previous large bowel polyps
– previous large bowel cancers
– cancers at other sites
– other risk factors for colorectal cancer
(IBD, acromegaly)
www.bowelcancerwest.org.uk
LOW RISK GROUP
Individuals
in this group have:
– no personal history of bowel cancer; no confirmed family
history of bowel cancer; or
– no first-degree relative (i.e. parent, sibling or child) with
bowel cancer; or
– one first-degree relative with bowel cancer diagnosed at
age 50 years or older
No
evidence to support invasive
surveillance
www.bowelcancerwest.org.uk
MODERATE RISK GROUP
Low-moderate
risk
– those with one affected relative
diagnosed under 50 years; or
– two affected first-degree relatives
diagnosed at at age 60 years or older
ONE OFF COLONOSCOPY AGE 55 YEARS
www.bowelcancerwest.org.uk
MODERATE RISK GROUP
High-moderate
risk
– three or more affected relatives in a first
degree kinship (none under 50 years)
– two affected relatives diagnosed under 60
years (or with a mean age at diagnosis
under 60 years) in a first degree kinship
5
YEARLY COLONOSCOPY FROM AGE
50 YEARS
www.bowelcancerwest.org.uk
HIGH RISK GROUP
Criteria include
– member of family with polyposis syndrome
– member of family with Lynch syndrome
– pedigree suggestive of autosomal dominantly
inherited colorectal (or other Lynch syndromeassociated) cancer
– pedigree indicative of autosomal recessive
inheritance, MYH associated polyposis (MAP)
Condition
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specific management
PEARLS AND PITFALLS
Family
history assessment of risk but
difficult to do well
If between risk groups, manage the
family as if in the higher risk group
Family histories evolve, risk group
change if cancers develop/excluded
ASPIRIN THE FUTURE?
www.bowelcancerwest.org.uk
ANY QUESTIONS?
www.bowelcancerwest.org.uk