The Cancer Genetics Service aims to:
- Provide an accessible service, which includes: risk assessment,
information, psychological, emotional and physical support of
individuals who are at increased risk of developing cancer due
to their family history.
- Use a multidisciplinary team approach to assess the needs of
individual patients, the appropriate level of intervention and
care can be suggested.
- Provide direct support and counselling to the 500 high risk
families already referred and for future referrals.
- Provide information, training, and support for healthcare professionals
who are involved in providing genetic information to families
through primary care or cancer clinics.
There has been a huge growth in referrals of families concerned
about the inherited basis of cancers over the last five years. They
now constitute over 30% of the departmental workload. In the main
this is centred on the common cancers of:
- familial breast cancer
- familial ovarian cancer
- familial bowel cancer
- hereditary non-polyposis colon cancer (HNPCC)
- familial adenomatous polyposis (FAP)
and the rarer, but more specific cancer predisposition syndromes:
- Von Hippel Lindau disease
- Gorlin's syndrome
- Neurofibromatosis type I and type II
- Li Fraumeni syndrome
- Ataxia Telangiectasia and chromosome breakage disorders
Mersey & Cheshire Clinical Genetics Service
- Cancer Genetics
Referral Guidelines for Patients Concerned
due to Family History Breast/Ovarian Cancer
The following criteria should be used to assess if your patient
is at increased risk of ovarian cancer and if she is likely to benefit
from referral to the Genetic Counselling Service at the Countess
of Chester Hospital. This clinic offers genetic risk assessment
and recommendations for clinical surveillance if appropriate. If
you feel that your patient would benefit from a genetic counselling
referral please discuss referral with a member of the genetics team.
Ovarian
Cancer Referral Guidelines |
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(all associated with at least 10%
ovarian cancer risk)
The family must be at increased risk
(as defined below).
The patient must be a first degree relative of an affected
family member.
- The family contains 2 or more individuals
on the same side of the family with ovarian cancer who are
first degree relatives of each other.
(or 2 close relatives on the same side of the family - please
discuss with a member of the genetics team).
or
- The family contains one individual
with ovarian cancer at any age and one individual with breast
cancer diagnosed under the age of 50 years, who are first
degree relatives of each other.
or
- The family contains one individual
with ovarian cancer at any age and two individuals with
breast cancer diagnosed under the age of 60 years who are
connected by first degree relationships.
or
- The family contains one individual
with one of the known cancer predisposing genes.
or
- The family contains three individuals
with colorectal cancer with at least one case diagnosed
before 50 years and one case of ovarian cancer connected
by first degree relationships.
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Breast
Cancer Referral Guidelines |

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Possible Moderate Risk Group
(Lifetime risk approximately 16 - 25%)
Breast cancer in:
1 first degree relative <40
or
1 first degree relative with
bilateral disease (first tumour <60)
or
1 male first degree relative
or
2 first degree relatives average
age <60
(e.g. mother-sister; two sisters)
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Refer
to local family history breast surveillance clinic.
Advise monthly breast self examination
Annual breast clinical examination
Baseline mammography at 35 years
Mammography every 12 months 40-50 years
Discharge to National Breast Screening Program at 50 years.
If below 35 re-refer at 35 or 5 years before youngest cancer
in the family.
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Possible
High Risk Group
(Lifetime risk approximately above 25%)
3 close relatives on the same side
of the family average age <60
or
2 close relatives average age <40
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Refer to local family history breast
surveillance clinic and to clinical genetics service (genetic
counselling)
Advise monthly breast self examination
Annual breast clinical examination to 60 years
Baseline mammography 35 years
Mammography every 12 months 40-50
Mammography every 18 months 50-60 to alternate with National
Breast Screening Program
Discharge at 60 years.
If below 35 re-refer at 35 or 5 years before youngest cancer
in the family.
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Referrals for high risk families should be made to:
Dr Ian Ellis or Dr Alan Fryer or Dr Anthony Ellis (Gastroenterology
Genetics)
Clinical Genetics - Referrals
Alder Hey Hospital
Eaton Road
Liverpool
L12 2AP
Partnership Clinics
This logo is used to identify services supported by the cancer
genetics service of the Merseyside and Cheshire Clinical genetics
Services. It is hoped to continue to support and develop a number
of breast cancer family history screening clinics across the zone
which will act as the first line contact for GP's wishing to refer
women.
The current partner Family History Breast Screening Clinics
are:
Sue Holcolme
Family History Breast Screening Clinic (Prof Leinster)
Royal Liverpool University Hospital
Prescot Road
Liverpool
L7 8XP
Family History Breast Screening Clinic
Southport and Formby District General Hospital
Town Lane
Southport
PR8 6PN
Ann Monahan
Breast Nurse
Family History Breast Screening Clinic
University Hospitals Aintree NHS Trust
WALTON
Rice Lane
Liverpool
L9
Miss Leena Chagla
Consultant Breast Surgeon in Whiston
Whiston Breast Services
Whiston Hospital
St Helen's and Knowsley Hospitals
Whiston Hospital
Prescot
Merseyside
L35 5DR
Miss Liz Redmond
Breast Screening Family History Clinic
Countess of Chester hospital
Liverpool Road Chester
CH2 1UL
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