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Breast
cancer
Breast
cancer is the most common female cancer in the UK. It is very
rare in women under 30, but for older women it becomes more
common. Men can also develop breast cancer, but this is happens
very rarely.
Around
one in nine women in the UK (11%) will develop breast cancer
during their lifetime. About 39,000 women are diagnosed in
the UK each year, and over 200 men.
Most
cases of breast cancer are not inherited (not caused by a
faulty gene which has been passed down from generation to
generation), but where a breast cancer gene is present it
greatly increases the risk that that person will develop the
disease. Men can carry the known breast cancer genes, but
they are very unlikely to get ill. However, men can pass the
gene on to their children.
So far, scientists have
identified two genes that are responsible for about 5 to 10%
of breast cancer cases. They can also increase a person's
risk of developing ovarian cancer. They are called BRCA1 and
BRCA2. It is quite likely that more genes will be found in
the future, but even then the vast majority of breast cancer
cases will occur without a strong family history (without
a genetic mutation having been passed down the generations) |
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Further
information can be found on this page about:
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London
IDEAS and breast cancer
About 1 in 20 cases (5
%) of breast cancer has a genetic link. London IDEAS is carrying
out several projects to improve access to breast cancer services
and to enhance awareness of genetics in breast cancer among health
professionals (particularly GPs, general practice nurses and midwives).
You can find out more about our work here.

Information
about breast cancer
There are several good
websites and publications for information about breast cancer, its
diagnosis and treatment.
Following
these links will take you specifically to background information

I
have breast changes – what next?
The first step is to see
your GP, who will examine you. You will be referred to a breast
cancer clinic if your GP thinks there is a possibility of cancer.
If you have attended an NHS Breast Screening Programme, you will
be referred in a similar manner if there is a suspicion of cancer.
Further information about
what happens next can be read about in this website:
To
find out what is known about diet and prevention of breast cancer,
follow these links:

Genetics
and breast cancer
Most breast cancer cases
are not inherited (not caused by a faulty gene that has been passed
down from generation to generation). Only about 1 in 20 cases (5
%) involve an inherited genetic factor. Many other aspects of a
woman's life can influence the development of breast cancer, such
the age at which she has children. It is also thought that there
are many other as yet unknown factors involved.
Two genes have been identified
so far that increase the risk of developing breast, and to a lesser
extent ovarian, cancer: BRCA1 and BRCA2. The child of a person with
one of these genes has a 50:50 (1 in 2) chance of inheriting the
same gene. Having one of these genes does not mean breast cancer
will definitely develop, but it does mean the risk is much greater
than for women who don't carry this particular genetic mutation.
Testing for cancer susceptibility
genes is a two-step process: the specific gene variation ("mutation")
in the family member with cancer must be found, then a predictive
gene test can be offered to unaffected family members.

Genetics,
patients and their families
The usefulness of genetic
testing in cancer susceptibility genes is probably over-rated by
both the general public and the medical profession and this has
led to very high demand in UK genetics centres from patients wanting
a genetic test.
Not everyone with a family
history of breast cancer is in a "high risk" category, and therefore
genetic testing is not suitable for the majority of people even
with some family history.
If you only have one,
or even two, elderly relatives who have had breast cancer, you are
still not at significantly increased risk of getting breast cancer
yourself. On the other hand, if your relatives were relatively young
when they got cancer, or if there are cases of bilateral cancer
(in both breasts), or of male breast cancer or breast and ovarian
cancer in your family, you are likely to be at significantly increased
risk.
Doctors seeing someone
with a family history will decide whether they are at low, moderate
or high risk:
- High risk families: two or more relatives with
breast and/or ovarian cancer, at least one of which was relatively
young when she got ill.
Members of these families
are cared for by health professionals working in cancer genetics,
breast care and primary care. They are offered genetic testing.
However, in the majority of cases no mutation is picked up.
- Moderate risk families: might have a number
of elderly relatives with breast cancer, or only one member with
breast cancer who got ill when she was very young (under 45).
Members of these families are cared for by the breast and primary
care teams in the NHS. Patients are offered regular mammographs.
Genetic testing is not normally necessary.
- Low risk families: might have one elderly member
with breast cancer.
Members of these families do not need further medical intervention,
but it is important that any anxieties are discussed, and that
individuals are reassured.

For
further information about breast cancer genetics:
CancerBACUP is developing
new information leaflets about genetics and cancer, and provides
an overview about breast cancer genetics on its website:
Breakthrough breast cancer
explains the issues that arise for people who are offered, or are
considering, taking a genetic test:
Further
information:
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